Inhibition of microRNA function by antimiR oligonucleotides
Silence volume 3, Article number: 1 (2012)
MicroRNAs (miRNAs) have emerged as important post-transcriptional regulators of gene expression in many developmental and cellular processes. Moreover, there is now ample evidence that perturbations in the levels of individual or entire families of miRNAs are strongly associated with the pathogenesis of a wide range of human diseases. Indeed, disease-associated miRNAs represent a new class of targets for the development of miRNA-based therapeutic modalities, which may yield patient benefits unobtainable by other therapeutic approaches. The recent explosion in miRNA research has accelerated the development of several computational and experimental approaches for probing miRNA functions in cell culture and in vivo. In this review, we focus on the use of antisense oligonucleotides (antimiRs) in miRNA inhibition for loss-of-function studies. We provide an overview of the currently employed antisense chemistries and their utility in designing antimiR oligonucleotides. Furthermore, we describe the most commonly used in vivo delivery strategies and discuss different approaches for assessment of miRNA inhibition and potential off-target effects. Finally, we summarize recent progress in antimiR mediated pharmacological inhibition of disease-associated miRNAs, which shows great promise in the development of novel miRNA-based therapeutics.
MicroRNAs (miRNAs) are an abundant class of small (approximately 22 nt) endogenous non-coding RNAs that direct post-transcriptional regulation of gene expression. Metazoan miRNAs regulate a wide range of biological processes, including developmental timing, apoptosis, differentiation, cell proliferation and metabolism [1–6]. Moreover, there is ample evidence that dysregulation of individual or entire families of miRNAs is associated with the pathogenesis of human diseases, such as cancer, CNS disorders, viral infections, cardiovascular and metabolic diseases [7–12].
The first miRNA genes, lin-4 and let-7, were discovered in C. elegans by Victor Ambros and Gary Ruvkun, and shown to base-pair imperfectly to 3' untranslated regions (UTRs) of heterochronic genes, thereby controlling timing of larval development in the worm [13–15]. To date 18,226 miRNAs have been annotated in animals, plants and viruses, including 1,527 miRNAs encoded in the human genome . miRNAs are either expressed from independent transcriptional units or derive from introns of protein-coding genes or exons or introns of long ncRNAs. Approximately 50% of the mammalian miRNAs are located within introns of protein-coding genes [17, 18]. The primary transcripts of miRNA genes, termed pri-miRNAs, are usually several kilobases long and possess a 5' CAP and a poly(A) tail [19, 20]. Pri-miRNAs are processed in the nucleus to approximately 70 nt hairpin-structures, known as pre-miRNAs (Figure 1), by the nuclear Microprocessor complex, consisting of DGCR8 and the RNase III enzyme Drosha [21–23]. Pre-miRNAs are exported to the cytoplasm by Exportin-5 [24–27] and processed further by Dicer, to approximately 22 nt double-stranded miRNA duplexes (Figure 1) [28–32]. The miRNA duplexes are loaded into an Argonaute protein in the miRNA-induced silencing complex (miRISC) and rapidly unwound. During this process the mature miRNA is retained in the miRISC, whereas the complementary strand, known as the miRNA star (miR*), is released [33, 34].
Most metazoan miRNAs guide the miRISC to partially complementary sites located in the 3' UTRs of target mRNAs, and, thereby, promote their translational repression or deadenylation and degradation [34, 35]. A key specificity determinant for miRNA target recognition is based on Watson-Crick pairing of the so-called seed region (nucleotides 2 to 8) in the mature miRNA to the seed match site in the target 3' UTR, which nucleates the miRNA:target mRNA interaction . The number of targets has been predicted using genome-wide computational searches for conserved seed match sites in mammalian 3' UTRs, which together with additional 3'-supplementary and 3'-compensatory binding sites imply that miRNAs may repress more than 60% of all mammalian protein-coding genes [36, 37].
Identification and experimental validation of miRNA targets is a key prerequisite for uncovering the widespread biological roles of miRNAs and miRNA-mediated gene regulatory networks. This has accelerated the development of several computational, biochemical, genetic and functional genomics approaches for miRNA studies [36, 38–44]. The most commonly used gain- and loss-of-function strategies to probe miRNA functions in vitro and in vivo are described in Table 1.
Currently, three approaches are used in miRNA loss-of-function studies: genetic knockouts, miRNA sponges and antisense oligonucleotides. Knockout mice lacking key miRNA processing factors, such as Dicer, Drosha and Ago2, are embryonic lethal, which demonstrates the general importance of miRNAs in early embryonic development . Generation of miRNA gene knockouts has been extensively used to unravel the functions of miRNAs in C. elegans and Drosophila, and has also been reported for many individual miRNAs in the mouse [8, 10, 65–71]. Recently, a genome-wide miRNA knockout resource covering 476 mouse miRNA genes was described, and has now been made available from ES cell repositories for distribution to the scientific community . The use of miRNA sponges, which are highly expressed transgenes harboring multiple miRNA target sites to sequester miRNAs, represents another strategy to modulate miRNA activity for loss-of-function studies . This approach enables both transient and long-term inhibition of entire miRNA seed families in cultured cells and has also been applied to manipulate miRNA activity in Drosophila and mice (reviewed by Ebert and Sharp ). Interestingly, systemic administration of a lentiviral sponge for miR-326 was shown to reduce the number of IL-17 secreting Th-17 cells and ameliorate experimental autoimmune encephalomyelitis (EAE) in mice . These findings highlight the potential of virally delivered miRNA sponges in the development of miRNA-based gene therapies.
A widely employed approach in miRNA loss-of-function studies is to use chemically modified antisense oligonucleotides, termed antimiRs, which sequester the mature miRNA in competition with cellular target mRNAs leading to functional inhibition of the miRNA and derepression of the direct targets (Figure 1). Here, we describe the current designs of chemically modified antimiR oligonucleotides and provide an overview of antimiR in vivo delivery strategies. In addition, we discuss the assessment of miRNA inhibition and off-target effects, as well as the utility of antimiR compounds in pharmacological inhibition of disease-implicated miRNAs for therapeutics.
Design of chemically modified antimiR oligonucleotides
MiRNA inhibition by antimiRs requires optimization of the oligonucleotides for increased binding affinity, improved nuclease resistance and in vivo delivery. This can be achieved using a variety of chemical modifications, including modifications of the sugar, the nucleobase or the internucleotide linkages (Figure 2A, B). Sequence-specific inhibition of miRNA function was first demonstrated in cultured HeLa cells using 2'-O-methyl (2'-O-Me) modified RNA oligonucleotides complementary to mature miRNAs [74, 75]. The 2'-O-Me modification as well as the 2'-O-methoxyethyl (2'-MOE) and 2'-fluoro (2'-F) chemistries are modified at the 2' position of the sugar moiety, whereas locked nucleic acid (LNA) comprises a class of bicyclic RNA analogues in which the furanose ring in the sugar-phosphate backbone is chemically locked in a RNA mimicking N-type (C3'-endo) conformation by the introduction of a 2'-O,4'-C methylene bridge (Figure 2A) [50, 76–80]. All the aforementioned modifications confer nuclease resistance and increase the binding affinity of antimiR oligonucleotides to their cognate miRNAs. Among these, LNA possesses the highest affinity towards complementary RNA with an increase in duplex melting temperature (Tm) of +2 to 8°C per introduced LNA monomer against complementary RNA compared to unmodified duplexes [80–83]. Another important observation is that LNA monomers are also able to twist the sugar conformation of flanking DNA nucleotides from an S-type (C2'-endo) towards an N-type sugar pucker in LNA-modified DNA oligonucleotides [80, 84]. Indeed, structural studies of different LNA-RNA and LNA-DNA heteroduplexes based on NMR spectroscopy and X-ray crystallography have shown that LNA-modified DNA oligonucleotides are RNA mimics, which fit seamlessly into an A-type Watson-Crick duplex geometry [84, 85] similar to that of dsRNA duplexes.
Nuclease resistance is also improved by backbone modification of the parent phosphodiester linkages into phosphorothioate (PS) linkages in which a sulfur atom replaces one of the non-bridging oxygen atoms in the phosphate group (Figure 2A) or by using morpholino oligomers, in which a six-membered morpholine ring replaces the sugar moiety. Morpholinos are uncharged, inherently resistant to degradation by nucleases and exhibit only a slight increase in binding affinity to miRNAs . Morpholino oligomers have been shown to be sequence-specific, non-toxic and potent inhibitors of both pri-miRNA and mature miRNA activity in zebrafish and Xenopus laevis [87–89].
Several studies have evaluated the potency of different chemically modified antimiR oligonucleotides in miRNA inhibition [76, 77, 90–93]. Two studies used luciferase reporter assays to compare different antimiR designs in targeting of miR-21 in HeLa cells. Davis et al.  showed a loose correlation between binding affinity and in vitro antimiR potency and found that among the fully PS modified antimiRs investigated, those with the highest Tm, a uniform 2'F and a LNA/2'-MOE mixmer antimiR, were the most potent miR-21 inhibitors. Similarly, Lennox and Behlke  reported that incorporation of high affinity modifications to antimiR oligonucleotides improved their potency. In their study, LNA/2'-O-Me mixmers with PS ends or with a complete PS backbone showed highest potency, being approximately 10 times more potent than a uniform 2'-O-Me modified antimiR. Consistent with these observations, we found that inhibition of miR-122 function in cultured Huh-7 cells by different LNA/DNA mixmers was affinity dependent and identified a LNA-modified antimiR with a high Tm of 80°C, which mediated efficient de-repression of a miR-122 luciferase reporter upon co-transfection of the antimiR-122 into Huh-7 cells at 5 nM concentration . Moreover, this antimiR-122 was also the most potent inhibitor of HCV RNA accumulation in Huh-7 cells harboring the HCV-N replicon, compared with a 2'-O-Me oligonucleotide and two LNA-antimiRs of lower affinity . Effective targeting of miR-122 by LNA/2'-O-Me and 2'-F/MOE modified antimiRs (Figure 2B), respectively, has also been reported [77, 94]. In most studies to date, fully complementary antimiRs have been used to target the mature miRNA. Notably, truncation of a uniform 2'-MOE-modified antimiR-21 and a cholesterol-conjugated antagomir-122, respectively, by three or more nucleotides was shown to result in substantial or complete loss of efficacy in cultured cells and in vivo [76, 95]. By comparison, we and others have reported on efficient antagonism of several miRNAs, using high-affinity 15 to 16 nucleotide LNA-modified DNA/PS oligonucleotides targeting the 5' region of the mature miRNA (Figure 2B) [11, 90, 96–102]. Furthermore, we have recently described a method that enables inhibition of miRNA function using short seed-targeting LNA oligonucleotides, designated as tiny LNAs . This approach exploits the high binding affinity of fully LNA-modified 8-mer PS oligonucleotides complementary to the miRNA seed region (Figure 2B, C), which enables specific and concentration-dependent inhibition of entire miRNA seed families in cultured cells with concomitant de-repression of direct targets . Our data highlight the importance of targeting the miRNA seed for inhibition, as 8-mer LNAs targeting other regions in mature miRNA sequences had no or limited effect on miRNA activity. The importance of the high binding affinity of fully substituted 8-mer LNAs was further demonstrated by the fact that an 8-mer 2'-O-Me-modified antimiR-21 oligonucleotide with a low Tm of 37°C showed no inhibition of miR-21 activity in HeLa cells .
In vivodelivery of antimiR oligonucleotides
Inhibition of miRNA function in vivo was first described in C. elegans by Hutvágner et al. . In this study, a 2'-O-Me oligonucleotide complementary to let-7 was microinjected in C. elegans larvae and shown to phenocopy the let-7 loss-of-function mutation . The utility of 3' cholesterol-conjugated, 2'-O-Me oligonucleotides with terminal PS modifications, termed antagomirs (Figure 2B), in pharmacological inhibition of miRNAs in mice, was described in 2005 by Krutzfeldt et al. . Treatment of mice with three tail vein injections of 80 mg/kg antagomir-16 resulted in silencing of miR-16 in the liver, kidney, lung, heart, skeletal muscle, colon, fat, skin, ovaries, adrenal glands and bone marrow, whereas no efficacy was observed in the brain . Furthermore, systemic delivery of antagomir-122 by three intravenous (i.v.) injections of 80 mg/kg led to efficient inhibition of the liver-expressed miR-122 with concomitant de-repression of liver mRNAs with miR-122 seed match sites and a 40% decrease in serum cholesterol levels in the treated mice . Subsequent studies showed that systemically delivered antagomir-122 accumulates in a cytoplasmic compartment of hepatocytes distinct from P-bodies and inferred an antagomir-mediated degradation mechanism independent of the RNAi pathway . Moreover, efficient inhibition of miR-16 in the brain was achieved by direct delivery of antagomir-16 in the mouse cortex .
PS backbone modifications greatly improve the pharmacokinetic properties of antisense oligonucleotides, thereby facilitating their delivery in vivo . Indeed, several studies have reported efficient and long-lasting silencing of miRNAs in vivo using unconjugated 2'-F/MOE-, 2'-MOE- and LNA-modified antimiRs harboring a complete PS backbone (Figure 2B) [11, 77, 90, 96, 97, 102, 106–108]. We have described potent and specific miR-122 silencing in vivo using a high-affinity 15 nucleotide LNA/DNA mixmer PS oligonucleotide complementary to the 5' end of miR-122 . Administration of unconjugated, saline-formulated LNA-antimiR-122 to mice either intraperitoneally (i.p.) or i.v. resulted in efficient uptake of the compound in the liver, which coincided with a dose-dependent sequestration of mature miR-122 in a highly stable heteroduplex with LNA-antimiR, inferring a different mode of action compared to the degradation mechanism described for antagomirs [95, 104] and 2'-MOE-modified oligonucleotides . Using single i.p. injections of the LNA-antimiR at doses ranging from 1 to 200 mg/kg we observed a dose-dependent lowering of serum cholesterol in mice with a median effective dose of 10 mg/kg, whereas treatment of high fat diet-fed mice with 5 mg/kg LNA-antimiR twice weekly for six weeks led to sustained lowering of serum cholesterol by 30% and de-repression of predicted target mRNAs with canonical miR-122 seed match sites . Moreover, systemic administration of PBS-formulated LNA-antimiR to African green monkeys at doses ranging from 1 to 10 mg/kg with three i.v. infusions over five days resulted in accumulation of the LNA-antimiR compound in the liver and concomitant, dose-dependent sequestration of mature miR-122 in a shifted LNA-antimiR:miR-122 heteroduplex in Northern blots. This led to a dose-dependent and long-lasting decrease of serum cholesterol in the treated primates, which gradually returned to baseline levels over a three-month period after treatment. Importantly, the LNA-antimiR compound was well tolerated in both mice and primates as no acute or subchronic toxicities in the treated animals were detected .
In a recent study, we investigated whether the high binding affinity of seed-targeting tiny 8-mer LNA-antimiRs could enable delivery and silencing of miRNAs in vivo without additional conjugation or formulation chemistries when combined with a complete PS backbone . A systemically delivered 8-mer antimiR-122 (three i.v. doses of 5 or 20 mg/kg) was shown to sequester miR-122 in the mouse liver, leading to concomitant de-repression of predicted miR-122 target mRNAs with canonical 3' UTR seed match sites and dose-dependent lowering of serum cholesterol, which is consistent with previous reports in rodents and non-human primates [90, 103, 104, 106]. Furthermore, a systemically delivered35S-labeled tiny antimiR-21 showed uptake in many tissues in mice with high levels of the compound accumulating in the kidney cortex, liver, lymph nodes, bone marrow and spleen with terminal half-lives ranging from 4 to 25 days . The terminal elimination half-life in heart blood was 8 to 10 hours and urine and bile were indicated as primary routes of elimination. The tiny antimiR-21 also sequestered the target miRNA in the liver, kidney and lung coinciding with up-regulation of the miR-21 target BTG2 in the same tissues . These findings imply that tiny LNAs could become a useful tool for functional studies of animal miRNAs in vivo, since unlike other chemically modified antimiRs, 8-mer LNAs enable inhibition of co-expressed miRNA family members that may have redundant biological functions.
Assessment of miRNA inhibition
The effect of miRNA inhibition by antimiR oligonucleotides can be assessed by a variety of approaches. Most methods that directly measure changes in miRNA levels are hybridization based assays and associated with several possible caveats when antimiR mediated miRNA inhibition is assessed. First, the antimiR chemistry appears to dictate the fate of the targeted miRNA. High-affinity oligonucleotides, such as LNA/DNA, LNA/2'-O-Me and 2'-F/MOE modified antimiRs, respectively, sequester the targeted miRNA in a heteroduplex [77, 90, 96, 102, 103, 107, 109], whereas lower affinity oligonucleotides, such as 2'-O-Me and 2'-MOE modified antimiRs and cholesterol-conjugated 2'-O-Me antagomirs, promote miRNA degradation [77, 104, 106, 109]. A recent study in Drosophila reported that extensive complementarity between Ago1-loaded miRNA and its target RNA can trigger tailing and 3'-to-5' exonucleolytic trimming of the miRNA causing a decrease in mature miRNA abundance . Notably, miRNA tailing and trimming were also observed in HeLa cells transfected with antagomirs fully complementary to miR-16 and miR-21, respectively , which is consistent with antagomir-mediated degradation of miRNAs descibed previously in mice . We and others have reported on detection of stable antimiR:miR heteroduplexes as slower-migrating bands on small RNA Northern blots (Figure 3) [90, 96, 102, 103, 107, 109, 111]. However, this can be technically challenging due to difficulties in the recovery and detection of the heteroduplexes . Second, the presence of excess antimiR in the RNA sample irrespective of the mechanism of action may interfere with the detection step of the assay, for example, primer annealing or extension in miRNA-specific real-time qPCR. The observed miRNA reduction in the readouts from such experiments could, therefore, be misleading due to the antimiR masking effects in the assays. Finally, antimiRs may be released from subcellular compartments during tissue homogenization and RNA extraction, thereby facilitating hybridization between the antimiR and the target miRNA during sample preparation. To help circumvent these pitfalls, especially for small RNA Northern blot analysis, it has been suggested to use stringent denaturing conditions during electrophoresis , to increase the hybridization temperature , to use LNA detection probes [90, 96, 103, 107, 112] or to include a competitor probe with an identical sequence as the miRNA prior to electrophoresis to release the miRNA from the miR:antimiR duplex [77, 109]. Taken together, due to the possible assay interference and technical difficulties in antimiR:miR heteroduplex recovery, evaluation of antimiR mediated inhibition of miRNA function by direct methods should be interpreted with some caution. Thus, we recommend that direct measurements of the targeted miRNA should always be accompanied with assessment of the functional effects after miRNA antagonism, as outlined in Figure 3.
Assays that measure a functional readout of miRNA modulation by antimiRs are often employed to provide substantial evidence for miRNA inhibition. These approaches include miRNA reporter assays, assessment of de-repression of direct targets by real-time qPCR, Western blot analysis and genome-wide transcriptional or proteomic analyses. A simple and very sensitive approach involves construction of a miRNA reporter that carries a single or multiple perfect match or bulged miRNA binding sites in the 3' UTR of a reporter gene, such as luciferase or GFP. This method has been extensively used in cultured cells to validate miRNA inhibition (Figure 3A) and also to compare the potency of different chemically modified antimiR designs [76, 90, 92, 103, 112]. Recently, a miR-21 luciferase reporter was used in a mouse mammary tumor model to monitor functional inhibition of miR-21 by a seed-targeting antimiR-21 in vivo . The antimiR specificity is typically assessed using control oligonucleotides, either by introducing one or more mismatches in the antimiR sequence or by using a scrambled sequence oligonucleotide. The potencies of such control oligonucleotides are expected to be markedly reduced, as shown in Figure 3B, in which the specificity of an 8-mer LNA-antimiR-21 was assessed by introducing one or two adjacent mismatches at all possible nucleotide positions in an 8-mer antimiR-21 sequence. Ideally, both control reporters with mutated miRNA target sites and mismatched or scrambled oligonucleotides should be included as specificity controls when assessing inhibition of miRNA function by miRNA reporter constructs.
The mechanism of miRNA-mediated mRNA repression involves both mRNA deadenylation and degradation and translational repression (Figure 1) [34, 35]. Recent reports on simultaneous genome-wide measurements of changes in mRNA and protein levels after perturbing miRNA levels showed good correlation between mRNA and protein levels [39, 40]. Thus, an alternative or supplemental approach to employing miRNA reporter assays is to use the levels of direct target mRNAs and their encoded proteins as functional readouts of miRNA silencing. Western blots are readily used to demonstrate the effect of antimiR mediated inhibition by assessing target de-repression at the protein level [103, 113–115]. However, the degree of miRNA target de-repression is often modest and several high throughput analyses following miRNA perturbation report changes in mRNA levels of only 33 to 35% [116, 117]. Moreover, proteomic studies that detect the effect of miRNA modulation by measuring directly the protein levels have reported that the average changes are less than two-fold [39, 40]. Hence, more sensitive methods, such as qPCR or ELISA, might be better suited to estimate antimiR effects on single direct targets, as shown in Figure 3E for two direct miR-122 target mRNAs in the mouse liver.
Given that a single miRNA has the potential to regulate hundreds of mRNA targets, high throughput methods that enable genome-wide transcriptional and proteomic profiling offer the opportunity to get a broad view of the effects of miRNA antagonism. Moreover, effects of perturbing the miRNA activity can be detected more robustly by assessing the combined effect on all the predicted direct targets. Thus, in the case where single target analysis is unable to find a significant effect, the simultaneous analysis of a large group of target mRNAs increases statistical power and can yield highly significant findings. Expression microarrays have been widely used in transcriptional profiling experiments and have also been employed by several studies to assess genome-wide transcriptional changes after modulation of miRNA activity in cultured cells and in vivo [37, 39, 40, 90, 103, 107, 118]. However, the recent development in massively parallel sequencing technologies has prompted many researchers to use RNA sequencing (RNA-Seq) for genome-wide expression analyses. RNA-Seq enables not only assessment of transcript levels with unprecedented accuracy and a broad dynamic range, but provides a detailed view of the entire transcriptome at a level that can provide important information on, for example, alternative splicing, RNA editing and other post-transcriptional modifications without the requirement of prior knowledge needed for microarray probe design . RNA-Seq was recently used to compare genome-wide transcriptional and proteomic changes mediated by ectopic and endogenous miRNAs in human and mouse cells [116, 117], and to assess antagomir-directed tailing and trimming of miRNAs in cultured HeLa cells .
A widely used method of testing the significance after modulation of miRNA activity on multiple targets is the Kolmogorov-Smirnov test, which asks whether the distribution of antimiR-mediated transcriptional changes observed for a set of target mRNAs is significantly different from a set of non-target mRNAs [37, 39, 40, 90, 103, 107, 118]. While this type of analysis is cut-off free, it requires a priori knowledge of miRNA targets and is, thus, biased by the choice of target prediction algorithm and by preselecting the miRNA targets for analysis. An alternative, more unbiased approach to analyzing the effect of miRNA perturbation on target mRNAs is to use the Sylamer algorithm  that uses expression changes measured after, for example, miRNA silencing to rank genes and subsequently test the occurrence of all possible sequence motifs of a given length relative to the sorted gene list. The landscape plots resulting from this type of analysis (Figure 3F) show the significance profiles of all sequence motifs of a given length across the sorted gene list, as shown in Figure 3F for two different LNA-modified antimiR oligonucleotides targeting miR-122.
Assessment of off-target effects
The use of antimiR oligonucleotides as a tool in functional miRNA studies or as a therapeutic modality carries the inherent risk of affecting RNA species other than the intended miRNA target. Thus, understanding the effects of unwanted interactions between the antimiR oligonucleotide and endogenous nucleic acids is of key importance and when appropriate, application of this knowledge during the design of antimiR molecules can help minimize off-target effects. The fact that longer oligonucleotides have fewer perfectly matched complementary sites in the transcriptome than shorter is sometimes used to state that longer oligonucleotides are more specific. However, this only holds true if the hybridization stringency can be controlled. When antimiRs are used in vivo, their interactions with RNA molecules are bound to take place at a physiologically relevant temperature and at reduced stringency. Thus, interactions are likely to occur through imperfect base pairing similar to, for example, non-specific priming observed in PCR at low annealing temperatures. The incorporation of chemical modifications, such as LNAs, into antimiRs, has been shown to improve mismatch discrimination , but this increased complexity versus simple Watson-Crick base pairing rules makes it difficult to accurately predict interaction sites for fully complementary antimiRs.
Due to their small size, 8-mer seed-targeting antimiRs have many predicted perfectly complementary sites in the transcriptome. Hence, by using Watson-Crick base pairing rules we are able to identify a substantial number of mRNAs that can be considered as candidates for off-targets. However, this does not necessarily imply that such sites are indeed occupied in the cell, nor is it given that such interactions if they occur have functional consequences by affecting the levels of the bound mRNAs or their encoded proteins. To address these questions, we have recently reported an empirical approach in which transcriptional and proteomic profiling was applied to measure the effects of tiny 8-mer LNAs in cell culture and in vivo . We first used the Sylamer algorithm  to ask which sequence motifs were associated with differentially expressed genes following tiny antimiR treatment. While the direct effect of tiny LNA mediated miRNA silencing was readily detected in all our experiments (Figure 3F and ) by significant overrepresentation of miRNA seed match sites in the up-regulated mRNAs, no enrichment of sequence motifs in mRNAs with tiny LNA complementary sites was detected. This implies that predicted off-targets are randomly distributed across the sorted gene lists, and that as a group, the predicted off-target mRNAs are not affected by the antimiR. Next, we used proteomic data to measure the effect of tiny LNAs on predicted off-targets to test whether potential binding of tiny LNAs to mRNAs could affect their translation. Our findings showed that the distribution of expression changes following tiny LNA mediated miRNA silencing differed significantly when miRNA targets were compared to non-targets, reflecting de-repression of direct targets. Contrary to the effect observed on the miRNA targets, the levels of proteins derived from mRNAs with tiny LNA complementary sites were not affected, implying that tiny LNAs do not have a general effect on predicted off-target interaction partners .
Another potential antimiR mediated off-target effect was recently reported by Khan et al. , who showed that transfection of miRNA mimetics or siRNAs into cells leads to effects on endogenous miRNA targets. These findings are consistent with a model in which the exogenous si/miRNA competes with the endogenous miRNA for miRISC and the consequent loss of available miRISC leads to abrogation of endogenous miRNA mediated regulation. Similar saturation-based effects could be detected when analyzing data sets from antimiR cell culture experiments, which implied that treatment with antimiRs leads to global effects on targets of other endogenous miRNAs. This is consistent with the notion that an antimiR oligonucleotide sequesters its cognate miRNA in the miRISC complex, thereby rendering it unavailable to other endogenous miRNAs. However, further experiments are needed to pinpoint the exact molecular mechanisms leading to the observed effects and to fully understand the ramifications these findings may have on endogenous miRNA function.
Therapeutic targeting of disease-associated miRNAs
Manipulation of miRNA activity in vivo is of high interest due to the aberrant expression and implication of miRNAs in the pathogenesis of human diseases. The use of antimiR oligonucleotides to target disease-associated miRNAs is the most widely used approach to probe their functions in vivo and shows great promise in the development of novel miRNA-based therapeutics. Indeed, an increasing number of studies have reported successful therapeutic miRNA silencing in a variety of animal disease models using antimiR oligonucleotides (Table 2). This section highlights selected studies, in which either 3' cholesterol-conjugated antagomirs or unconjugated, chemically modified antimiRs harboring a complete PS backbone have been used to pharmacologically inhibit disease-associated miRNAs in vivo.
In an orthotopic xenograft model of metastatic breast cancer, 4T1 cells were implanted into the mammary fat pad of mice and miR-10b was targeted by antagomir-10b to investigate the effects of the primary tumors and their metastatic capacity . This is a very aggressive metastasis model and, therefore, antagomir treatment was initiated already at day 2 after implantation to interfere with early stages of metastasis. The antagomir compound was administered i.v. twice weekly for three weeks (50 mg/kg) and mice were analyzed at day 28. Treatment did not reduce primary mammary tumor growth of 4T1 cells, whereas a striking suppression in the formation of lung metastases was observed (86% reduction of pulmonary metastases). The inhibition of miR-10b was validated by qRT-PCR and de-repression of the direct miR-10b target Hoxd10. Specificity was demonstrated by unaltered levels of miR-9 and miR-21 that are reported to be up-regulated in breast tumors and unchanged miR-10a, which differs by only 1 nt compared to the mature miR-10b sequence. In addition, a miR-10b sponge approach phenocopied the antagomir data, whereas no effect of miR-10b inhibition on lung metastases from disseminated cells (tail vein injected 4T1 cells) was observed, suggesting that miR-10b is not involved in late stage metastasis. The tolerability and toxicity of the antagomir treatment was assessed by several parameters, including behavior, body, lung and heart weight, respectively, white blood cell and lymphocyte count, histopathological investigations of steatosis, inflammation, necrosis, fibrosis and biliary changes. The most noticeable changes were the lowering of white blood cells and lymphocytes for miR-10b antagomir and as a suggested antagomir class effect; increased liver and spleen size, and elevated serum levels of bilirubin, ALT and AST .
Recently, miR-103 and miR-107 were shown to directly regulate insulin sensitivity in vivo . This miRNA family was up-regulated in the liver of diet-induced obese and ob/ob mice, which led to decreased insulin sensitivity and enhanced hepatic glucose production. Cholesterol-conjugated antagomir-103 was applied to investigate the function of miR-103/107 in diabetes and administered via the tail vein on two consecutive days (15 mg/kg/dose). Targeting of miR-103/107 was demonstrated by Northern blot analysis, qRT-PCR and de-repression of the direct target Caveolin-1, whereas specificity was shown using mismatched and scrambled antagomirs. Silencing of miR-103/107 lowered plasma glucose levels in obese but not in wild-type mice, and improved glucose homeostasis and insulin sensitivity. Furthermore, over-expression or antagomir mediated silencing of miR-103/107 in diet-induced obese mice lacking Caveolin-1 demonstrated a central role of Caveolin-1 in mediating the miR-103/107 effects on glucose tolerance and insulin sensitivity .
Systemic lupus erythematosus (SLE) is a chronic autoimmune disease, in which a combination of genetic predisposition and possible environmental factors triggers an immune response directed against ubiquitous, mostly intranuclear, self-antigens. Antibody production by B cells and abnormal antibody-independent B and T cell functions imply that B and T cells are important in the pathogenesis of SLE (reviewed in [132, 133]). The B6.Sle123 mouse strain bears three lupus susceptibility loci and develops an autoimmune syndrome that strongly resembles human lupus disease, characterized by autoantibody production, lymphosplenomegaly and glomerulonephritis. In a recent study, miR-21 was found to be up-regulated in B and T cells of B6.Sle123 mice , consistent with findings in another genetic mouse model of lupus as well as in human lupus CD4+ T cells and B cells [134, 135]. Silencing of miR-21 by i.p. delivered, unconjugated 8-mer seed-targeting antimiR-21 reversed splenomegaly, one of the cardinal manifestations of autoimmunity in B6.Sle123 mice and de-repressed PDCD4 expression in vivo. In addition, antimiR-21 treatment altered CD4+/CD8+ T cell ratios towards those of the non-autoimmune control mice and reduced Fas receptor-expressing B cells, suggesting that miR-21 plays a critical role in regulating autoimmune responses in lupus. Furthermore, these findings imply that tiny seed-targeting LNAs can be used to inhibit miRNAs in peripheral lymphocytes in vivo and that pharmacological inhibition of miR-21 by an 8-mer antimiR-21 can alter the course of a systemic autoimmune disease in lupus mice .
The miR-208a/b family and miR-499, designated as MyomiRs, are located in the introns of three myosin genes, Myh6, Myh7, and Myh7b, respectively, and play critical roles in the control of pathological cardiac hypertrophy, heart failure and myocardial infarction in humans and mouse models of heart disease [10, 136]. Genetic deletion of miR-208 in mice showed no phenotype at baseline, whereas in response to cardiac stress, miR-208 knockout mice showed virtually no cardiomyocyte hypertrophy or fibrosis [137, 138]. In a recent study, Montgomery et al.  investigated the cardioprotective effect of miR-208a loss-of-function in hypertensive rats. Therapeutic silencing of miR-208a by subcutaneously (s.c.) delivered LNA-modified antimiR-208a led to potent and sustained silencing of miR-208a in the rat heart. Notably, the antimiR treatment prevented pathological myosin switching and cardiac remodeling during hypertension-induced heart failure in Dahl hypertensive rats, and resulted in improved cardiac function, overall health and survival. These data highlight the potential of antimiR-based approaches to pharmacologically inhibit cardiac miRNAs and strongly imply miR-208 as a therapeutic target for treatment of heart disease .
Perturbations in cholesterol homeostasis and lipid metabolism are associated with several life-threatening diseases, such as atherosclerosis, type II diabetes and metabolic syndrome. In 2010, a number of independent studies reported that miR-33a, which is embedded within an intron of the sterol regulatory element-binding protein-2 (SREBP2) gene, targets the ATP-binding cassette transporter A1 (ABCA1), an important regulator of high-density lipoprotein (HDL) synthesis and reverse cholesterol transport, for post-transcriptional repression [11, 12, 129, 139, 140]. Interestingly, another member of the miR-33 family, miR-33b, is found within an intron of the SREBP-1c gene in human and primates, whereas mice only have one miR-33 isoform corresponding to miR-33a . The mature sequences of miR-33a and miR-33b differ by only two nucleotides and share the same seed region, implying that the two miR-33 family members have overlapping targets, and, thus, redundant biological functions, including regulation of cholesterol efflux in cells. Three in vivo studies have used antimiR oligonucleotides to probe the functions of miR-33 in cholesterol homeostasis in the mouse. Marquart et al.  delivered antimiRs intravenously (5 mg/kg/dose on three consecutive days) and showed increased ABCA1 expression and HDL-cholesterol levels in serum 12 days after administration, whereas Najafi-Shoushtari et al.  injected a LNA-modified antimiR-33 i.v. at a dose of 20 mg/kg for three consecutive days, which resulted in efficient inhibition of miR-33 and concomitant increase of HDL-C by 25% in the mouse serum. More recently, a third in vivo study targeting miR-33 was reported, in which low-density lipoprotein (LDL) receptor knockout mice with established atherosclerotic plaques were treated with s.c. delivered 2'F/MOE antimiR for four weeks (two s.c. injections of 10 mg/kg the first week followed by weekly injections of 10 mg/kg) . Treatment of Ldlr-/- mice with antimiR-33 led to elevated circulating HDL-C levels and enhanced reverse cholesterol transport to the plasma, liver and feces. Moreover, several markers of atherosclerotic plaque stability were increased, which was consistent with plaque regression and lesion remodelling in antimiR-33 treated mice. Importantly, this study showed that antimiR-33 oligonucleotides are able to penetrate the atherosclerotic lesion to reach plaque macrophages, in which they can enhance ABCA1 expression and cholesterol removal . Together, these studies demonstrate that pharmacological inhibition of miR-33 in vivo by antimiR-33 oligonucleotides raises circulating HDL-C levels, enhances reverse cholesterol transport and regresses atherosclerosis, implying that therapeutic silencing of miR-33 could be a useful strategy for the treatment of cardiovascular disease.
Therapeutic targeting of microRNA-122 for treatment of hepatitis C virus infection
Hepatitis C virus (HCV) infection is a leading cause of liver disease worldwide with over 180 million infected individuals who are at greatly increased risk of developing liver failure and hepatocellular carcinoma (HCC). The current standard therapy, which combines pegylated interferon-α with ribavirin provides sustained virologic response rates in only about 50% of patients and is also associated with many side effects . New targeted HCV therapies, including viral polymerase and protease inhibitors have yielded encouraging results, but the emergence of viral escape mutations during such therapies requires a combination with other HCV drugs to tackle viral resistance . By comparison, therapeutic approaches that target essential host functions for HCV may provide a high barrier to resistance and, thus, could provide an alternative strategy for the development of new HCV therapeutics. The liver-expressed miR-122 binds to two closely spaced miR-122 target sites in the 5' non-coding region (NCR) of the HCV genome, resulting in up-regulation of viral RNA levels . This unusual interaction was first described by Peter Sarnow in 2005 , and was subsequently confirmed by several reports [144–146], implying that miR-122 is an essential host factor for HCV RNA accumulation in infected liver cells. Notably, inhibition of miR-122 by antimiR oligonucleotides leads to rapid loss of HCV RNA in cultured liver cells, which makes miR-122 an attractive therapeutic target for antiviral intervention [143, 146]. In a recent study, Machlin et al.  investigated the contributions of the two miR-122 molecules by assessing the effects of miR-122 point mutations on HCV viral RNA abundance. The data from stepwise mutational analyses suggest a model for an oligomeric miR-122-HCV complex in which one miR-122 molecule binds to the 5' terminus of the HCV RNA with 3' overhanging nucleotides masking the 5' terminal sequences of the HCV genome. These findings suggest that miR-122 protects the 5' terminal viral sequences from nucleolytic degradation or from inducing innate immune responses to the RNA terminus .
Besides its role in modulating cholesterol homeostasis and promoting HCV RNA abundance, miR-122 has also been suggested to be important for maintaining liver cell identity and reported to be down-regulated in HCC [148–150]. Loss of miR-122 expression in HCC was shown to be associated with poor prognosis, acquisition of an invasive phenotype and with intrahepatic metastasis [150–152]. The tumor-suppressive effects of miR-122 have been linked to several direct miR-122 targets implicated in HCC tumorigenesis, such as cyclin G1, RHOA and the metalloprotease ADAM17. Interestingly, other studies have reported that miR-122 expression is either maintained or increased in HCV-associated HCC [150, 153]. Moreover, Varnholt et al.  observed strong up-regulation of miR-122 in an extended sample set of HCV-induced dysplastic nodules and HCCs, which implies that the role of miR-122 in HCV-derived HCCs is different compared to that in HCCs of non-HCV etiologies. While further studies are needed to establish the potential risks associated with long-term therapeutic silencing of miR-122, it is important to note that short-term inhibition of miR-122 in rodents and non-human primates was shown to be reversible [90, 96], and furthermore, that the duration of treatment of HCV-infected patients with an antimiR-122 is expected to be limited.
Several studies have reported on pharmacological inhibition of miR-122 in mice using antimiR oligonucleotides [77, 90, 96, 100, 104, 106]. We have previously shown that potent miR-122 antagonism can be achieved in rodents and non-human primates using a high-affinity 15-mer LNA-modified antimiR-122. In this study, systemic delivery of unconjugated, saline-formulated antimiR-122 resulted in efficient sequestration of miR-122 leading to a dose-dependent and long-lasting decrease of serum cholesterol levels in mice and African green monkeys without any evidence for acute or subchronic toxicities in the study animals . Moreover, this antimiR oligonucleotide was highly potent in inhibiting HCV RNA accumulation in Huh-7 cells harboring the HCV-N replicon NNeo/C-5B . More recently, we assessed the potential of miR-122 antagonism as a new anti-HCV therapy in chimpanzees with chronic HCV infection . In this study, four chimpanzees infected with HCV genotype 1 were treated with i.v. injections of the 15 nt LNA-antimiR-122 on a weekly basis for 12 weeks, followed by a treatment-free period of about 12 weeks after dosing. Treatment of the HCV-infected chimpanzees led to long-lasting suppression of HCV viremia with no evidence for viral resistance or side effects in the treated animals. Furthermore, transcriptional profiling and histopathology of liver biopsies demonstrated de-repression of target mRNAs with canonical miR-122 seed sites, down-regulation of interferon-regulated genes and improvement of HCV-induced liver pathology . The long-lasting suppression of HCV viremia without viral rebound implies that the antimiR-122 approach has a high barrier to viral resistance. Furthermore, the fact that both miR-122 seed sites are conserved in all HCV genotypes suggests that the antiviral effect of antimiR-122 will be genotype-independent, which was recently confirmed .
Indeed, this antimiR-122 compound, termed miravirsen, is the first miRNA-targeted drug to enter human clinical trials. Data from phase 1 single (up to 12 mg/kg) and multiple ascending dose (up to five doses of 5 mg/kg) safety studies in 77 healthy volunteers showed that miravirsen is well tolerated, has an attractive pharmacokinetic profile and clear dose-dependent pharmacology. Importantly, no dose limiting toxicities were identified [155, 156]. In September 2010, Santaris Pharma A/S advanced miravirsen into a phase 2a trial to assess the safety, tolerability, pharmacokinetics and antiviral activity of miravirsen in treatment-naïve patients with chronic HCV genotype 1 infection [155, 156]. In this multiple ascending dose study patients were enrolled sequentially to one of three cohorts (nine active and three placebo per cohort) and miravirsen was administered at doses of 3, 5 or 7 mg/kg as a total of five weekly subcutaneous injections over 29 days. Treatment with miravirsen provided robust, dose-dependent anti-viral activity with a mean reduction of two to three logs from baseline in HCV RNA (log10 IU/mL) that was maintained for more than four weeks after the last dose of miravirsen. Notably, four out of nine patients treated at the highest dose (7 mg/kg) became HCV RNA undetectable during the study [155, 156]. No serious adverse events were observed and only mild and infrequent adverse events, such as headache, coryza and diarrhea were reported. Furthermore, there were no clinically significant changes in safety tests, vital signs or electrocardiograms [155, 156]. As expected, pharmacological inhibition of miR-122 in HCV patients resulted in decreased levels of serum cholesterol, apoA and apoB. Taken together, these data indicate that miravirsen given as a four-week monotherapy to HCV patients provides long-lasting suppression of viremia, has a high barrier to viral resistance and is well tolerated in patients with chronic HCV infection.
The challenge of unravelling the myriad roles of hundreds of miRNAs in many developmental and cellular processes as well as in human disease pathogenesis calls for continuous development of robust computational and experimental approaches for studying miRNA functions in cell culture and in vivo. Inhibition of miRNA function by chemically modified antimiR oligonucleotides has become an important and widely used approach in miRNA loss-of-function studies and enables inhibition of both single miRNAs and entire miRNA seed families. Despite recent advances in the design and use of antimiRs, experiments that seek to inhibit miRNA function are associated with several possible pitfalls when antimiR mediated miRNA inhibition is assessed. Furthermore, the use of antimiR oligonucleotides as tools in miRNA loss-of-function studies or as therapeutic modalities carries the inherent risk of affecting RNA species other than the intended miRNA target. Hence, adequate assessment of the functional effects after miRNA inhibition and the physiological repercussions of long-term miRNA antagonism in vivo, as well as understanding the potential off-target effects resulting from unwanted interactions between the antimiR oligonucleotide and endogenous nucleic acids, are of key importance for antimiR-based miRNA loss-of-function studies and for the development of miRNA therapeutics.
Efficient in vivo delivery of antimiR oligonucleotides is another critical factor for their successful use in vivo and for the development of miRNA-based therapeutic modalities. Many peripheral tissues can be effectively targeted by systemically delivered chemically modified antimiR oligonucleotides, which show good pharmacokinetic properties and tissue uptake along with high stability in blood and tissues in vivo. A number of alternative strategies for delivery of antisense oligonucleotides and siRNAs are being pursued and these could also be applied to antimiRs. For example, ligands for specific cell surface receptors capable of being internalized can be conjugated to oligonucleotides, thereby facilitating both cellular uptake and cell type-specific delivery. Nevertheless, recent findings that unconjugated, saline-formulated antimiR oligonucleotides can be used in miRNA silencing in vivo suggest that antimiRs are useful tools for validating disease-associated miRNA targets in animal disease models. Furthermore, the high potency and metabolic stability of chemically modified antimiRs, and the lack of acute and subchronic toxicities in rodents and non-human primates highlights the potential of antimiRs in the development of novel therapeutic modalities based on disease-associated miRNAs. Indeed, recent data from the first phase 2 study in patients with chronic HCV genotype 1 infection treated with the LNA-modified antimiR-122 drug miravirsen showed that this compound was well tolerated and provided long-lasting suppression of viremia in HCV-infected patients.
ATP-binding cassette transporter A1
antisense oligonucleotides that inhibit miRNA function
central nervous system
diet induced obesity
experimental autoimmune encephalomyelitis
hepatitis C virus
locked nucleic acid
miRNA-induced silencing complex
systemic lupus erythematosus
sterol regulatory element-binding protein-2
Ambros V: The functions of animal microRNAs. Nature. 2004, 431: 350-355. 10.1038/nature02871.
Kloosterman WP, Plasterk RH: The diverse functions of microRNAs in animal development and disease. Dev Cell. 2006, 11: 441-450. 10.1016/j.devcel.2006.09.009.
Bushati N, Cohen SM: microRNA functions. Annu Rev Cell Dev Biol. 2007, 23: 175-205. 10.1146/annurev.cellbio.23.090506.123406.
Lima RT, Busacca S, Almeida GM, Gaudino G, Fennell DA, Vasconcelos MH: MicroRNA regulation of core apoptosis pathways in cancer. Eur J Cancer. 2011, 47: 163-174. 10.1016/j.ejca.2010.11.005.
Braun T, Gautel M: Transcriptional mechanisms regulating skeletal muscle differentiation, growth and homeostasis. Nat Rev Mol Cell Biol. 2011, 12: 349-361. 10.1038/nrm3118.
Ambros V: MicroRNAs and developmental timing. Curr Opin Genet Dev. 2011, 21: 511-517. 10.1016/j.gde.2011.04.003.
Gottwein E, Cullen BR: Viral and cellular microRNAs as determinants of viral pathogenesis and immunity. Cell Host Microbe. 2008, 3: 375-387. 10.1016/j.chom.2008.05.002.
Williams AH, Liu N, van Rooij E, Olson EN: MicroRNA control of muscle development and disease. Curr Opin Cell Biol. 2009, 21: 461-469. 10.1016/j.ceb.2009.01.029.
Ventura A, Jacks T: MicroRNAs and cancer: short RNAs go a long way. Cell. 2009, 136: 586-591. 10.1016/j.cell.2009.02.005.
van Rooij E, Quiat D, Johnson BA, Sutherland LB, Qi X, Richardson JA, Kelm RJ, Olson EN: A family of microRNAs encoded by myosin genes governs myosin expression and muscle performance. Dev Cell. 2009, 17: 662-673. 10.1016/j.devcel.2009.10.013.
Najafi-Shoushtari SH, Kristo F, Li Y, Shioda T, Cohen DE, Gerszten RE, Naar AM: MicroRNA-33 and the SREBP host genes cooperate to control cholesterol homeostasis. Science. 2010, 328: 1566-1569. 10.1126/science.1189123.
Rayner KJ, Suarez Y, Davalos A, Parathath S, Fitzgerald ML, Tamehiro N, Fisher EA, Moore KJ, Fernandez-Hernando C: MiR-33 contributes to the regulation of cholesterol homeostasis. Science. 2010, 328: 1570-1573. 10.1126/science.1189862.
Lee RC, Feinbaum RL, Ambros V: The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14. Cell. 1993, 75: 843-854. 10.1016/0092-8674(93)90529-Y.
Wightman B, Ha I, Ruvkun G: Posttranscriptional regulation of the heterochronic gene lin-14 by lin-4 mediates temporal pattern formation in C. elegans. Cell. 1993, 75: 855-862. 10.1016/0092-8674(93)90530-4.
Reinhart BJ, Slack FJ, Basson M, Pasquinelli AE, Bettinger JC, Rougvie AE, Horvitz HR, Ruvkun G: The 21-nucleotide let-7 RNA regulates developmental timing in Caenorhabditis elegans. Nature. 2000, 403: 901-906. 10.1038/35002607.
Kozomara A, Griffiths-Jones S: miRBase: integrating microRNA annotation and deep-sequencing data. Nucleic Acids Res. 2011, 39: D152-D157. 10.1093/nar/gkq1027.
Rodriguez A, Griffiths-Jones S, Ashurst JL, Bradley A: Identification of mammalian microRNA host genes and transcription units. Genome Res. 2004, 14: 1902-1910. 10.1101/gr.2722704.
Griffiths-Jones S: Annotating noncoding RNA genes. Annu Rev Genomics Hum Genet. 2007, 8: 279-298. 10.1146/annurev.genom.8.080706.092419.
Lee Y, Kim M, Han J, Yeom KH, Lee S, Baek SH, Kim VN: MicroRNA genes are transcribed by RNA polymerase II. EMBO J. 2004, 23: 4051-4060. 10.1038/sj.emboj.7600385.
Cai X, Hagedorn CH, Cullen BR: Human microRNAs are processed from capped, polyadenylated transcripts that can also function as mRNAs. RNA. 2004, 10: 1957-1966. 10.1261/rna.7135204.
Lee Y, Ahn C, Han J, Choi H, Kim J, Yim J, Lee J, Provost P, Radmark O, Kim S, Kim VN: The nuclear RNase III Drosha initiates microRNA processing. Nature. 2003, 425: 415-419. 10.1038/nature01957.
Denli AM, Tops BB, Plasterk RH, Ketting RF, Hannon GJ: Processing of primary microRNAs by the Microprocessor complex. Nature. 2004, 432: 231-235. 10.1038/nature03049.
Gregory RI, Yan KP, Amuthan G, Chendrimada T, Doratotaj B, Cooch N, Shiekhattar R: The Microprocessor complex mediates the genesis of microRNAs. Nature. 2004, 432: 235-240. 10.1038/nature03120.
Murchison EP, Hannon GJ: miRNAs on the move: miRNA biogenesis and the RNAi machinery. Curr Opin Cell Biol. 2004, 16: 223-229. 10.1016/j.ceb.2004.04.003.
Lund E, Guttinger S, Calado A, Dahlberg JE, Kutay U: Nuclear export of microRNA precursors. Science. 2004, 303: 95-98. 10.1126/science.1090599.
Yi R, Qin Y, Macara IG, Cullen BR: Exportin-5 mediates the nuclear export of pre-microRNAs and short hairpin RNAs. Genes Dev. 2003, 17: 3011-3016. 10.1101/gad.1158803.
Bohnsack MT, Czaplinski K, Gorlich D: Exportin 5 is a RanGTP-dependent dsRNA-binding protein that mediates nuclear export of pre-miRNAs. RNA. 2004, 10: 185-191. 10.1261/rna.5167604.
Bernstein E, Caudy AA, Hammond SM, Hannon GJ: Role for a bidentate ribonuclease in the initiation step of RNA interference. Nature. 2001, 409: 363-366. 10.1038/35053110.
Grishok A, Pasquinelli AE, Conte D, Li N, Parrish S, Ha I, Baillie DL, Fire A, Ruvkun G, Mello CC: Genes and mechanisms related to RNA interference regulate expression of the small temporal RNAs that control C. elegans developmental timing. Cell. 2001, 106: 23-34. 10.1016/S0092-8674(01)00431-7.
Hutvagner G, McLachlan J, Pasquinelli AE, Balint E, Tuschl T, Zamore PD: A cellular function for the RNA-interference enzyme Dicer in the maturation of the let-7 small temporal RNA. Science. 2001, 293: 834-838. 10.1126/science.1062961.
Ketting RF, Fischer SE, Bernstein E, Sijen T, Hannon GJ, Plasterk RH: Dicer functions in RNA interference and in synthesis of small RNA involved in developmental timing in C. elegans. Genes Dev. 2001, 15: 2654-2659. 10.1101/gad.927801.
Knight SW, Bass BL: A role for the RNase III enzyme DCR-1 in RNA interference and germ line development in Caenorhabditis elegans. Science. 2001, 293: 2269-2271. 10.1126/science.1062039.
Carthew RW, Sontheimer EJ: Origins and Mechanisms of miRNAs and siRNAs. Cell. 2009, 136: 642-655. 10.1016/j.cell.2009.01.035.
Krol J, Loedige I, Filipowicz W: The widespread regulation of microRNA biogenesis, function and decay. Nat Rev Genet. 2010, 11: 597-610.
Huntzinger E, Izaurralde E: Gene silencing by microRNAs: contributions of translational repression and mRNA decay. Nat Rev Genet. 2011, 12: 99-110. 10.1038/nrg2936.
Bartel DP: MicroRNAs: target recognition and regulatory functions. Cell. 2009, 136: 215-233. 10.1016/j.cell.2009.01.002.
Friedman RC, Farh KK, Burge CB, Bartel DP: Most mammalian mRNAs are conserved targets of microRNAs. Genome Res. 2009, 19: 92-105.
Lim LP, Lau NC, Garrett-Engele P, Grimson A, Schelter JM, Castle J, Bartel DP, Linsley PS, Johnson JM: Microarray analysis shows that some microRNAs downregulate large numbers of target mRNAs. Nature. 2005, 433: 769-773. 10.1038/nature03315.
Baek D, Villen J, Shin C, Camargo FD, Gygi SP, Bartel DP: The impact of microRNAs on protein output. Nature. 2008, 455: 64-71. 10.1038/nature07242.
Selbach M, Schwanhausser B, Thierfelder N, Fang Z, Khanin R, Rajewsky N: Widespread changes in protein synthesis induced by microRNAs. Nature. 2008, 455: 58-63. 10.1038/nature07228.
Chi SW, Zang JB, Mele A, Darnell RB: Argonaute HITS-CLIP decodes microRNA-mRNA interaction maps. Nature. 2009, 460: 479-486.
Hafner M, Landthaler M, Burger L, Khorshid M, Hausser J, Berninger P, Rothballer A, Ascano M, Jungkamp AC, Munschauer M, Ulrich A, Wardle GS, Dewell S, Zavolan M, Tuschl T: Transcriptome-wide identification of RNA-binding protein and microRNA target sites by PAR-CLIP. Cell. 2010, 141: 129-141. 10.1016/j.cell.2010.03.009.
Park CY, Choi YS, McManus MT: Analysis of microRNA knockouts in mice. Hum Mol Genet. 2010, 19: R169-R175. 10.1093/hmg/ddq367.
Krek A, Grun D, Poy MN, Wolf R, Rosenberg L, Epstein EJ, MacMenamin P, da Piedade I, Gunsalus KC, Stoffel M, Rajewsky N: Combinatorial microRNA target predictions. Nat Genet. 2005, 37: 495-500. 10.1038/ng1536.
Ebert MS, Sharp PA: MicroRNA sponges: progress and possibilities. RNA. 2010, 16: 2043-2050. 10.1261/rna.2414110.
Ebert MS, Sharp PA: Emerging roles for natural microRNA sponges. Curr Biol. 2010, 20: R858-R861. 10.1016/j.cub.2010.08.052.
Du C, Liu C, Kang J, Zhao G, Ye Z, Huang S, Li Z, Wu Z, Pei G: MicroRNA miR-326 regulates TH-17 differentiation and is associated with the pathogenesis of multiple sclerosis. Nat Immunol. 2009, 10: 1252-1259. 10.1038/ni.1798.
Broderick JA, Zamore PD: MicroRNA therapeutics. Gene Ther. 2011, 18: 1104-1110. 10.1038/gt.2011.50.
van Rooij E: The art of microRNA research. Circ Res. 2011, 108: 219-234. 10.1161/CIRCRESAHA.110.227496.
Stenvang J, Kauppinen S: MicroRNAs as targets for antisense-based therapeutics. Expert Opin Biol Ther. 2008, 8: 59-81. 10.1517/147125220.127.116.11.
Staton AA, Knaut H, Giraldez AJ: miRNA regulation of Sdf1 chemokine signaling provides genetic robustness to germ cell migration. Nat Genet. 2011, 43: 204-211. 10.1038/ng.758.
Choi WY, Giraldez AJ, Schier AF: Target protectors reveal dampening and balancing of Nodal agonist and antagonist by miR-430. Science. 2007, 318: 271-274. 10.1126/science.1147535.
Xiao J, Yang B, Lin H, Lu Y, Luo X, Wang Z: Novel approaches for gene-specific interference via manipulating actions of microRNAs: examination on the pacemaker channel genes HCN2 and HCN4. J Cell Physiol. 2007, 212: 285-292. 10.1002/jcp.21062.
Stittrich AB, Haftmann C, Sgouroudis E, Kuhl AA, Hegazy AN, Panse I, Riedel R, Flossdorf M, Dong J, Fuhrmann F, Heinz GA, Fang Z, Li N, Bissels U, Hatam F, Jahn A, Hammoud B, Matz M, Schulze FM, Baumgrass R, Bosio A, Mollenkopf HJ, Grun J, Thiel A, Chen W, Hofer T, Loddenkemper C, Lohning M, Chang HD, Rajewsky N, et al: The microRNA miR-182 is induced by IL-2 and promotes clonal expansion of activated helper T lymphocytes. Nat Immunol. 2010, 11: 1057-1062. 10.1038/ni.1945.
Jordan SD, Kruger M, Willmes DM, Redemann N, Wunderlich FT, Bronneke HS, Merkwirth C, Kashkar H, Olkkonen VM, Bottger T, Braun T, Seibler J, Bruning JC: Obesity-induced overexpression of miRNA-143 inhibits insulin-stimulated AKT activation and impairs glucose metabolism. Nat Cell Biol. 2011, 13: 434-446. 10.1038/ncb2211.
Hatley ME, Patrick DM, Garcia MR, Richardson JA, Bassel-Duby R, van Rooij E, Olson EN: Modulation of K-Ras-dependent lung tumorigenesis by MicroRNA-21. Cancer Cell. 2010, 18: 282-293. 10.1016/j.ccr.2010.08.013.
Bader AG, Brown D, Winkler M: The promise of microRNA replacement therapy. Cancer Res. 2010, 70: 7027-7030. 10.1158/0008-5472.CAN-10-2010.
Henry JC, Azevedo-Pouly AC, Schmittgen TD: microRNA replacement therapy for cancer. Pharm Res. 2011, 28: 3030-3042. 10.1007/s11095-011-0548-9.
Trang P, Medina PP, Wiggins JF, Ruffino L, Kelnar K, Omotola M, Homer R, Brown D, Bader AG, Weidhaas JB, Slack FJ: Regression of murine lung tumors by the let-7 microRNA. Oncogene. 2010, 29: 1580-1587. 10.1038/onc.2009.445.
Esquela-Kerscher A, Trang P, Wiggins JF, Patrawala L, Cheng A, Ford L, Weidhaas JB, Brown D, Bader AG, Slack FJ: The let-7 microRNA reduces tumor growth in mouse models of lung cancer. Cell Cycle. 2008, 7: 759-764. 10.4161/cc.7.6.5834.
Wiggins JF, Ruffino L, Kelnar K, Omotola M, Patrawala L, Brown D, Bader AG: Development of a lung cancer therapeutic based on the tumor suppressor microRNA-34. Cancer Res. 2010, 70: 5923-5930. 10.1158/0008-5472.CAN-10-0655.
Trang P, Wiggins JF, Daige CL, Cho C, Omotola M, Brown D, Weidhaas JB, Bader AG, Slack FJ: Systemic delivery of tumor suppressor microRNA mimics using a neutral lipid emulsion inhibits lung tumors in mice. Mol Ther. 2011, 19: 1116-1122. 10.1038/mt.2011.48.
Garzon R, Marcucci G, Croce CM: Targeting microRNAs in cancer: rationale, strategies and challenges. Nat Rev Drug Discov. 2010, 9: 775-789. 10.1038/nrd3179.
Kota J, Chivukula RR, O'Donnell KA, Wentzel EA, Montgomery CL, Hwang HW, Chang TC, Vivekanandan P, Torbenson M, Clark KR, Mendell JR, Mendell JT: Therapeutic microRNA delivery suppresses tumorigenesis in a murine liver cancer model. Cell. 2009, 137: 1005-1017. 10.1016/j.cell.2009.04.021.
Abbott AL, Alvarez-Saavedra E, Miska EA, Lau NC, Bartel DP, Horvitz HR, Ambros V: The let-7 MicroRNA family members mir-48, mir-84, and mir-241 function together to regulate developmental timing in Caenorhabditis elegans. Dev Cell. 2005, 9: 403-414. 10.1016/j.devcel.2005.07.009.
Sokol NS, Ambros V: Mesodermally expressed Drosophila microRNA-1 is regulated by Twist and is required in muscles during larval growth. Genes Dev. 2005, 19: 2343-2354. 10.1101/gad.1356105.
Miska EA, Alvarez-Saavedra E, Abbott AL, Lau NC, Hellman AB, McGonagle SM, Bartel DP, Ambros VR, Horvitz HR: Most Caenorhabditis elegans microRNAs are individually not essential for development or viability. PLoS Genet. 2007, 3: e215-10.1371/journal.pgen.0030215.
Johnnidis JB, Harris MH, Wheeler RT, Stehling-Sun S, Lam MH, Kirak O, Brummelkamp TR, Fleming MD, Camargo FD: Regulation of progenitor cell proliferation and granulocyte function by microRNA-223. Nature. 2008, 451: 1125-1129. 10.1038/nature06607.
Ventura A, Young AG, Winslow MM, Lintault L, Meissner A, Erkeland SJ, Newman J, Bronson RT, Crowley D, Stone JR, Jaenisch R, Sharp PA, Jacks T: Targeted deletion reveals essential and overlapping functions of the miR-17 through 92 family of miRNA clusters. Cell. 2008, 132: 875-886. 10.1016/j.cell.2008.02.019.
van Rooij E, Sutherland LB, Thatcher JE, DiMaio JM, Naseem RH, Marshall WS, Hill JA, Olson EN: Dysregulation of microRNAs after myocardial infarction reveals a role of miR-29 in cardiac fibrosis. Proc Natl Acad Sci USA. 2008, 105: 13027-13032. 10.1073/pnas.0805038105.
Mu P, Han YC, Betel D, Yao E, Squatrito M, Ogrodowski P, de Stanchina E, D'Andrea A, Sander C, Ventura A: Genetic dissection of the miR-17-92 cluster of microRNAs in Myc-induced B-cell lymphomas. Genes Dev. 2009, 23: 2806-2811. 10.1101/gad.1872909.
Prosser HM, Koike-Yusa H, Cooper JD, Law FC, Bradley A: A resource of vectors and ES cells for targeted deletion of microRNAs in mice. Nat Biotechnol. 2011, 29: 840-845. 10.1038/nbt.1929.
Ebert MS, Neilson JR, Sharp PA: MicroRNA sponges: competitive inhibitors of small RNAs in mammalian cells. Nat Methods. 2007, 4: 721-726. 10.1038/nmeth1079.
Hutvagner G, Simard MJ, Mello CC, Zamore PD: Sequence-specific inhibition of small RNA function. PLoS Biol. 2004, 2: E98-10.1371/journal.pbio.0020098.
Meister G, Landthaler M, Dorsett Y, Tuschl T: Sequence-specific inhibition of microRNA- and siRNA-induced RNA silencing. RNA. 2004, 10: 544-550. 10.1261/rna.5235104.
Davis S, Lollo B, Freier S, Esau C: Improved targeting of miRNA with antisense oligonucleotides. Nucleic Acids Res. 2006, 34: 2294-2304. 10.1093/nar/gkl183.
Davis S, Propp S, Freier SM, Jones LE, Serra MJ, Kinberger G, Bhat B, Swayze EE, Bennett CF, Esau C: Potent inhibition of microRNA in vivo without degradation. Nucleic Acids Res. 2009, 37: 70-77. 10.1093/nar/gkn904.
Esau CC: Inhibition of microRNA with antisense oligonucleotides. Methods. 2008, 44: 55-60. 10.1016/j.ymeth.2007.11.001.
Esau CC, Monia BP: Therapeutic potential for microRNAs. Adv Drug Deliv Rev. 2007, 59: 101-114. 10.1016/j.addr.2007.03.007.
Petersen M, Wengel J: LNA: a versatile tool for therapeutics and genomics. Trends Biotechnol. 2003, 21: 74-81. 10.1016/S0167-7799(02)00038-0.
Braasch DA, Corey DR: Locked nucleic acid (LNA): fine-tuning the recognition of DNA and RNA. Chem Biol. 2001, 8: 1-7. 10.1016/S1074-5521(00)00058-2.
Koshkin AA, Singh SK, Nielsen P, Rajwanshi VK, Kumar R, Meldgaard M, Olsen CE, Wengel J: LNA (Locked Nucleic Acids): synthesis of the adenine, cytosine, guanine, 5-methylcytosine, thymine and uracil bicyclonucleoside monomers, oligomerisation, and unprecedented nucleic acid recognition. Tetrahedron. 1998, 54: 3607-3630. 10.1016/S0040-4020(98)00094-5.
Obika S, Nanbu D, Hari Y, Andoh Ji, Morio Ki, Doi T, Imanishi T: Stability and structural features of the duplexes containing nucleoside analogues with a fixed N-type conformation, 2'-O,4'-C-methyleneribonucleosides. Tetrahedron Letters. 1998, 39: 5401-5404. 10.1016/S0040-4039(98)01084-3.
Petersen M, Bondensgaard K, Wengel J, Jacobsen JP: Locked nucleic acid (LNA) recognition of RNA: NMR solution structures of LNA:RNA hybrids. J Am Chem Soc. 2002, 124: 5974-5982. 10.1021/ja012288d.
Nielsen KE, Rasmussen J, Kumar R, Wengel J, Jacobsen JP, Petersen M: NMR studies of fully modified locked nucleic acid (LNA) hybrids: solution structure of an LNA:RNA hybrid and characterization of an LNA:DNA hybrid. Bioconjug Chem. 2004, 15: 449-457. 10.1021/bc034145h.
Summerton J, Weller D: Morpholino antisense oligomers: design, preparation, and properties. Antisense Nucleic Acid Drug Dev. 1997, 7: 187-195. 10.1089/oli.1.1997.7.187.
Martello G, Zacchigna L, Inui M, Montagner M, Adorno M, Mamidi A, Morsut L, Soligo S, Tran U, Dupont S, Cordenonsi M, Wessely O, Piccolo S: MicroRNA control of Nodal signalling. Nature. 2007, 449: 183-188. 10.1038/nature06100.
Flynt AS, Li N, Thatcher EJ, Solnica-Krezel L, Patton JG: Zebrafish miR-214 modulates Hedgehog signaling to specify muscle cell fate. Nat Genet. 2007, 39: 259-263. 10.1038/ng1953.
Kloosterman WP, Lagendijk AK, Ketting RF, Moulton JD, Plasterk RH: Targeted inhibition of miRNA maturation with morpholinos reveals a role for miR-375 in pancreatic islet development. PLoS Biol. 2007, 5: e203-10.1371/journal.pbio.0050203.
Elmen J, Lindow M, Schutz S, Lawrence M, Petri A, Obad S, Lindholm M, Hedtjarn M, Hansen HF, Berger U, Gullans S, Kearney P, Sarnow P, Straarup EM, Kauppinen S: LNA-mediated microRNA silencing in non-human primates. Nature. 2008, 452: 896-899. 10.1038/nature06783.
Fabani MM, Abreu-Goodger C, Williams D, Lyons PA, Torres AG, Smith KG, Enright AJ, Gait MJ, Vigorito E: Efficient inhibition of miR-155 function in vivo by peptide nucleic acids. Nucleic Acids Res. 2010, 38: 4466-4475. 10.1093/nar/gkq160.
Lennox KA, Behlke MA: A direct comparison of anti-microRNA oligonucleotide potency. Pharm Res. 2010, 27: 1788-1799. 10.1007/s11095-010-0156-0.
Lennox KA, Behlke MA: Chemical modification and design of anti-miRNA oligonucleotides. Gene Ther. 2011, 18: 1111-1120. 10.1038/gt.2011.100.
Fabani MM, Gait MJ: miR-122 targeting with LNA/2'-O-methyl oligonucleotide mixmers, peptide nucleic acids (PNA), and PNA-peptide conjugates. RNA. 2008, 14: 336-346.
Krutzfeldt J, Kuwajima S, Braich R, Rajeev KG, Pena J, Tuschl T, Manoharan M, Stoffel M: Specificity, duplex degradation and subcellular localization of antagomirs. Nucleic Acids Res. 2007, 35: 2885-2892. 10.1093/nar/gkm024.
Elmen J, Lindow M, Silahtaroglu A, Bak M, Christensen M, Lind-Thomsen A, Hedtjarn M, Hansen JB, Hansen HF, Straarup EM, McCullagh K, Kearney P, Kauppinen S: Antagonism of microRNA-122 in mice by systemically administered LNA-antimiR leads to up-regulation of a large set of predicted target mRNAs in the liver. Nucleic Acids Res. 2008, 36: 1153-1162.
Worm J, Stenvang J, Petri A, Frederiksen KS, Obad S, Elmen J, Hedtjarn M, Straarup EM, Hansen JB, Kauppinen S: Silencing of microRNA-155 in mice during acute inflammatory response leads to derepression of c/ebp Beta and down-regulation of G-CSF. Nucleic Acids Res. 2009, 37: 5784-5792. 10.1093/nar/gkp577.
Nicolas FE, Pais H, Schwach F, Lindow M, Kauppinen S, Moulton V, Dalmay T: Experimental identification of microRNA-140 targets by silencing and overexpressing miR-140. RNA. 2008, 14: 2513-2520. 10.1261/rna.1221108.
Kocerha J, Faghihi MA, Lopez-Toledano MA, Huang J, Ramsey AJ, Caron MG, Sales N, Willoughby D, Elmen J, Hansen HF, Orum H, Kauppinen S, Kenny PJ, Wahlestedt C: MicroRNA-219 modulates NMDA receptor-mediated neurobehavioral dysfunction. Proc Natl Acad Sci USA. 2009, 106: 3507-3512. 10.1073/pnas.0805854106.
Castoldi M, Vujic SM, Altamura S, Elmen J, Lindow M, Kiss J, Stolte J, Sparla R, D'Alessandro LA, Klingmuller U, Fleming RE, Longerich T, Grone HJ, Benes V, Kauppinen S, Hentze MW, Muckenthaler MU: The liver-specific microRNA miR-122 controls systemic iron homeostasis in mice. J Clin Invest. 2011, 121: 1386-1396. 10.1172/JCI44883.
Eskildsen T, Taipaleenmaki H, Stenvang J, Abdallah BM, Ditzel N, Nossent AY, Bak M, Kauppinen S, Kassem M: MicroRNA-138 regulates osteogenic differentiation of human stromal (mesenchymal) stem cells in vivo. Proc Natl Acad Sci USA. 2011, 108: 6139-6144. 10.1073/pnas.1016758108.
Montgomery RL, Hullinger TG, Semus HM, Dickinson BA, Seto AG, Lynch JM, Stack C, Latimer PA, Olson EN, van Rooij E: Therapeutic inhibition of miR-208a improves cardiac function and survival during heart failure. Circulation. 2011, 124: 1537-1547. 10.1161/CIRCULATIONAHA.111.030932.
Obad S, dos Santos CO, Petri A, Heidenblad M, Broom O, Ruse C, Fu C, Lindow M, Stenvang J, Straarup EM, Hansen HF, Koch T, Pappin D, Hannon GJ, Kauppinen S: Silencing of microRNA families by seed-targeting tiny LNAs. Nat Genet. 2011, 43: 371-378. 10.1038/ng.786.
Krutzfeldt J, Rajewsky N, Braich R, Rajeev KG, Tuschl T, Manoharan M, Stoffel M: Silencing of microRNAs in vivo with 'antagomirs'. Nature. 2005, 438: 685-689. 10.1038/nature04303.
Levin AA: A review of the issues in the pharmacokinetics and toxicology of phosphorothioate antisense oligonucleotides. Biochim Biophys Acta. 1999, 1489: 69-84.
Esau C, Davis S, Murray SF, Yu XX, Pandey SK, Pear M, Watts L, Booten SL, Graham M, McKay R, Subramaniam A, Propp S, Lollo BA, Freier S, Bennett CF, Bhanot S, Monia BP: miR-122 regulation of lipid metabolism revealed by in vivo antisense targeting. Cell Metab. 2006, 3: 87-98. 10.1016/j.cmet.2006.01.005.
Lanford RE, Hildebrandt-Eriksen ES, Petri A, Persson R, Lindow M, Munk ME, Kauppinen S, Orum H: Therapeutic silencing of microRNA-122 in primates with chronic hepatitis C virus infection. Science. 2010, 327: 198-201. 10.1126/science.1178178.
Rayner KJ, Sheedy FJ, Esau CC, Hussain FN, Temel RE, Parathath S, van Gils JM, Rayner AJ, Chang AN, Suarez Y, Fernandez-Hernando C, Fisher EA, Moore KJ: Antagonism of miR-33 in mice promotes reverse cholesterol transport and regression of atherosclerosis. J Clin Invest. 2011, 121: 2921-2931. 10.1172/JCI57275.
Torres AG, Fabani MM, Vigorito E, Gait MJ: MicroRNA fate upon targeting with anti-miRNA oligonucleotides as revealed by an improved Northern-blot-based method for miRNA detection. RNA. 2011, 17: 933-943. 10.1261/rna.2533811.
Ameres SL, Horwich MD, Hung JH, Xu J, Ghildiyal M, Weng Z, Zamore PD: Target RNA-directed trimming and tailing of small silencing RNAs. Science. 2010, 328: 1534-1539. 10.1126/science.1187058.
Patrick DM, Montgomery RL, Qi X, Obad S, Kauppinen S, Hill JA, van Rooij E, Olson EN: Stress-dependent cardiac remodeling occurs in the absence of microRNA-21 in mice. J Clin Invest. 2010, 120: 3912-3916. 10.1172/JCI43604.
Horwich MD, Zamore PD: Design and delivery of antisense oligonucleotides to block microRNA function in cultured Drosophila and human cells. Nat Protoc. 2008, 3: 1537-1549. 10.1038/nprot.2008.145.
Mayr C, Hemann MT, Bartel DP: Disrupting the pairing between let-7 and Hmga2 enhances oncogenic transformation. Science. 2007, 315: 1576-1579. 10.1126/science.1137999.
Yu F, Yao H, Zhu P, Zhang X, Pan Q, Gong C, Huang Y, Hu X, Su F, Lieberman J, Song E: let-7 regulates self renewal and tumorigenicity of breast cancer cells. Cell. 2007, 131: 1109-1123. 10.1016/j.cell.2007.10.054.
Garchow BG, Encinas OB, Leung YT, Tsao PY, Eisenberg RA, Caricchio R, Obad S, Petri A, Kauppinen S, Kiriakidou M: Silencing of microRNA-21 in vivo ameliorates autoimmune splenomegaly in lupus mice. EMBO Mol Med. 2011, 3: 605-615. 10.1002/emmm.201100171.
Hendrickson DG, Hogan DJ, McCullough HL, Myers JW, Herschlag D, Ferrell JE, Brown PO: Concordant regulation of translation and mRNA abundance for hundreds of targets of a human microRNA. PLoS Biol. 2009, 7: e1000238-10.1371/journal.pbio.1000238.
Guo H, Ingolia NT, Weissman JS, Bartel DP: Mammalian microRNAs predominantly act to decrease target mRNA levels. Nature. 2010, 466: 835-840. 10.1038/nature09267.
Grimson A, Farh KK, Johnston WK, Garrett-Engele P, Lim LP, Bartel DP: MicroRNA targeting specificity in mammals: determinants beyond seed pairing. Mol Cell. 2007, 27: 91-105. 10.1016/j.molcel.2007.06.017.
Wang Z, Gerstein M, Snyder M: RNA-Seq: a revolutionary tool for transcriptomics. Nat Rev Genet. 2009, 10: 57-63. 10.1038/nrg2484.
van Dongen S, Abreu-Goodger C, Enright AJ: Detecting microRNA binding and siRNA off-target effects from expression data. Nat Methods. 2008, 5: 1023-1025. 10.1038/nmeth.1267.
You Y, Moreira BG, Behlke MA, Owczarzy R: Design of LNA probes that improve mismatch discrimination. Nucleic Acids Res. 2006, 34: e60-10.1093/nar/gkl175.
Khan AA, Betel D, Miller ML, Sander C, Leslie CS, Marks DS: Transfection of small RNAs globally perturbs gene regulation by endogenous microRNAs. Nat Biotechnol. 2009, 27: 549-555.
Ma L, Reinhardt F, Pan E, Soutschek J, Bhat B, Marcusson EG, Teruya-Feldstein J, Bell GW, Weinberg RA: Therapeutic silencing of miR-10b inhibits metastasis in a mouse mammary tumor model. Nat Biotechnol. 2010, 28: 341-347. 10.1038/nbt.1618.
Anand S, Majeti BK, Acevedo LM, Murphy EA, Mukthavaram R, Scheppke L, Huang M, Shields DJ, Lindquist JN, Lapinski PE, King PD, Weis SM, Cheresh DA: MicroRNA-132-mediated loss of p120RasGAP activates the endothelium to facilitate pathological angiogenesis. Nat Med. 2010, 16: 909-914. 10.1038/nm.2186.
da Costa Martins PA, Salic K, Gladka MM, Armand AS, Leptidis S, el Azzouzi H, Hansen A, Coenen-de Roo CJ, Bierhuizen MF, van der Nagel R, van Kuik J, de Weger R, de Bruin A, Condorelli G, Arbones ML, Eschenhagen T, De Windt LJ: MicroRNA-199b targets the nuclear kinase Dyrk1a in an auto-amplification loop promoting calcineurin/NFAT signalling. Nat Cell Biol. 2010, 12: 1220-1227. 10.1038/ncb2126.
Lu Y, Zhang Y, Wang N, Pan Z, Gao X, Zhang F, Zhang Y, Shan H, Luo X, Bai Y, Sun L, Song W, Xu C, Wang Z, Yang B: MicroRNA-328 contributes to adverse electrical remodeling in atrial fibrillation. Circulation. 2010, 122: 2378-2387. 10.1161/CIRCULATIONAHA.110.958967.
Fontana L, Fiori ME, Albini S, Cifaldi L, Giovinazzi S, Forloni M, Boldrini R, Donfrancesco A, Federici V, Giacomini P, Peschle C, Fruci D: Antagomir-17-5p abolishes the growth of therapy-resistant neuroblastoma through p21 and BIM. PLoS One. 2008, 3: e2236-10.1371/journal.pone.0002236.
Trajkovski M, Hausser J, Soutschek J, Bhat B, Akin A, Zavolan M, Heim MH, Stoffel M: MicroRNAs 103 and 107 regulate insulin sensitivity. Nature. 2011, 474: 649-653. 10.1038/nature10112.
Marquart TJ, Allen RM, Ory DS, Baldan A: miR-33 links SREBP-2 induction to repression of sterol transporters. Proc Natl Acad Sci USA. 2010, 107: 12228-12232. 10.1073/pnas.1005191107.
Swarbrick A, Woods SL, Shaw A, Balakrishnan A, Phua Y, Nguyen A, Chanthery Y, Lim L, Ashton LJ, Judson RL, Huskey N, Blelloch R, Haber M, Norris MD, Lengyel P, Hackett CS, Preiss T, Chetcuti A, Sullivan CS, Marcusson EG, Weiss W, L'Etoile N, Goga A: miR-380-5p represses p53 to control cellular survival and is associated with poor outcome in MYCN-amplified neuroblastoma. Nat Med. 2010, 16: 1134-1140. 10.1038/nm.2227.
Long J, Wang Y, Wang W, Chang BH, Danesh FR: MicroRNA-29c is a signature microRNA under high glucose conditions that targets Sprouty homolog 1, and its in vivo knockdown prevents progression of diabetic nephropathy. J Biol Chem. 2011, 286: 11837-11848. 10.1074/jbc.M110.194969.
Crispin JC, Liossis SN, Kis-Toth K, Lieberman LA, Kyttaris VC, Juang YT, Tsokos GC: Pathogenesis of human systemic lupus erythematosus: recent advances. Trends Mol Med. 2010, 16: 47-57. 10.1016/j.molmed.2009.12.005.
Sanz I, Lee FE: B cells as therapeutic targets in SLE. Nat Rev Rheumatol. 2010, 6: 326-337. 10.1038/nrrheum.2010.68.
Pan W, Zhu S, Yuan M, Cui H, Wang L, Luo X, Li J, Zhou H, Tang Y, Shen N: MicroRNA-21 and microRNA-148a contribute to DNA hypomethylation in lupus CD4+ T cells by directly and indirectly targeting DNA methyltransferase 1. J Immunol. 2010, 184: 6773-6781. 10.4049/jimmunol.0904060.
Te JL, Dozmorov IM, Guthridge JM, Nguyen KL, Cavett JW, Kelly JA, Bruner GR, Harley JB, Ojwang JO: Identification of unique microRNA signature associated with lupus nephritis. PLoS One. 2010, 5: e10344-10.1371/journal.pone.0010344.
Small EM, Frost RJ, Olson EN: MicroRNAs add a new dimension to cardiovascular disease. Circulation. 2010, 121: 1022-1032. 10.1161/CIRCULATIONAHA.109.889048.
van Rooij E, Sutherland LB, Qi X, Richardson JA, Hill J, Olson EN: Control of stress-dependent cardiac growth and gene expression by a microRNA. Science. 2007, 316: 575-579. 10.1126/science.1139089.
Callis TE, Pandya K, Seok HY, Tang RH, Tatsuguchi M, Huang ZP, Chen JF, Deng Z, Gunn B, Shumate J, Willis MS, Selzman CH, Wang DZ: MicroRNA-208a is a regulator of cardiac hypertrophy and conduction in mice. J Clin Invest. 2009, 119: 2772-2786. 10.1172/JCI36154.
Gerin I, Clerbaux LA, Haumont O, Lanthier N, Das AK, Burant CF, Leclercq IA, MacDougald OA, Bommer GT: Expression of miR-33 from an SREBP2 intron inhibits cholesterol export and fatty acid oxidation. J Biol Chem. 2010, 285: 33652-33661. 10.1074/jbc.M110.152090.
Horie T, Ono K, Horiguchi M, Nishi H, Nakamura T, Nagao K, Kinoshita M, Kuwabara Y, Marusawa H, Iwanaga Y, Hasegawa K, Yokode M, Kimura T, Kita T: MicroRNA-33 encoded by an intron of sterol regulatory element-binding protein 2 (Srebp2) regulates HDL in vivo. Proc Natl Acad Sci USA. 2010, 107: 17321-17326. 10.1073/pnas.1008499107.
Chisari FV: Unscrambling hepatitis C virus-host interactions. Nature. 2005, 436: 930-932. 10.1038/nature04076.
De Francesco R, Migliaccio G: Challenges and successes in developing new therapies for hepatitis C. Nature. 2005, 436: 953-960. 10.1038/nature04080.
Jopling CL, Yi M, Lancaster AM, Lemon SM, Sarnow P: Modulation of hepatitis C virus RNA abundance by a liver-specific MicroRNA. Science. 2005, 309: 1577-1581. 10.1126/science.1113329.
Randall G, Panis M, Cooper JD, Tellinghuisen TL, Sukhodolets KE, Pfeffer S, Landthaler M, Landgraf P, Kan S, Lindenbach BD, Chien M, Weir DB, Russo JJ, Ju J, Brownstein MJ, Sheridan R, Sander C, Zavolan M, Tuschl T, Rice CM: Cellular cofactors affecting hepatitis C virus infection and replication. Proc Natl Acad Sci USA. 2007, 104: 12884-12889. 10.1073/pnas.0704894104.
Henke JI, Goergen D, Zheng J, Song Y, Schuttler CG, Fehr C, Junemann C, Niepmann M: microRNA-122 stimulates translation of hepatitis C virus RNA. EMBO J. 2008, 27: 3300-3310. 10.1038/emboj.2008.244.
Jopling CL, Schutz S, Sarnow P: Position-dependent function for a tandem microRNA miR-122-binding site located in the hepatitis C virus RNA genome. Cell Host Microbe. 2008, 4: 77-85. 10.1016/j.chom.2008.05.013.
Machlin ES, Sarnow P, Sagan SM: Masking the 5' terminal nucleotides of the hepatitis C virus genome by an unconventional microRNA-target RNA complex. Proc Natl Acad Sci USA. 2011, 108: 3193-3198. 10.1073/pnas.1012464108.
Kutay H, Bai S, Datta J, Motiwala T, Pogribny I, Frankel W, Jacob ST, Ghoshal K: Downregulation of miR-122 in the rodent and human hepatocellular carcinomas. J Cell Biochem. 2006, 99: 671-678. 10.1002/jcb.20982.
Gramantieri L, Ferracin M, Fornari F, Veronese A, Sabbioni S, Liu CG, Calin GA, Giovannini C, Ferrazzi E, Grazi GL, Croce CM, Bolondi L, Negrini M: Cyclin G1 is a target of miR-122a, a microRNA frequently down-regulated in human hepatocellular carcinoma. Cancer Res. 2007, 67: 6092-6099. 10.1158/0008-5472.CAN-06-4607.
Coulouarn C, Factor VM, Andersen JB, Durkin ME, Thorgeirsson SS: Loss of miR-122 expression in liver cancer correlates with suppression of the hepatic phenotype and gain of metastatic properties. Oncogene. 2009, 28: 3526-3536. 10.1038/onc.2009.211.
Tsai WC, Hsu PW, Lai TC, Chau GY, Lin CW, Chen CM, Lin CD, Liao YL, Wang JL, Chau YP, Hsu MT, Hsiao M, Huang HD, Tsou AP: MicroRNA-122, a tumor suppressor microRNA that regulates intrahepatic metastasis of hepatocellular carcinoma. Hepatology. 2009, 49: 1571-1582. 10.1002/hep.22806.
Fornari F, Gramantieri L, Giovannini C, Veronese A, Ferracin M, Sabbioni S, Calin GA, Grazi GL, Croce CM, Tavolari S, Chieco P, Negrini M, Bolondi L: MiR-122/cyclin G1 interaction modulates p53 activity and affects doxorubicin sensitivity of human hepatocarcinoma cells. Cancer Res. 2009, 69: 5761-5767. 10.1158/0008-5472.CAN-08-4797.
Varnholt H, Drebber U, Schulze F, Wedemeyer I, Schirmacher P, Dienes HP, Odenthal M: MicroRNA gene expression profile of hepatitis C virus-associated hepatocellular carcinoma. Hepatology. 2008, 47: 1223-1232.
Li YP, Gottwein JM, Scheel TK, Jensen TB, Bukh J: MicroRNA-122 antagonism against hepatitis C virus genotypes 1-6 and reduced efficacy by host RNA insertion or mutations in the HCV 5' UTR. Proc Natl Acad Sci USA. 2011, 108: 4991-4996. 10.1073/pnas.1016606108.
Santaris Pharma a/s. [http://www.santaris.com]
Janssen HL, Reesink HW, Zeuzem S, Lawitz E, Rodriguez-Torres M, Chen A, Davis C, King B, Levin AA, Hodges MR: A randomized, double-blind, placebo (plb) controlled safety and anti-viral proof of concept study of miravirsen (MIR), an oligonucleotide targeting miR-122, in treatment naïve patients with genotype 1 (gt1) chronic HCV infection [abstract]. Hepatology. 2011, 54: 1430A-
AP, ML, SO and SK are employees of Santaris Pharma, a clinical stage biopharmaceutical company that develops RNA-directed therapeutics. JS has no competing interests.
JS, AP and SK drafted the manuscript with input from SO and ML. All authors reviewed and approved the final manuscript.
About this article
Cite this article
Stenvang, J., Petri, A., Lindow, M. et al. Inhibition of microRNA function by antimiR oligonucleotides. Silence 3, 1 (2012). https://doi.org/10.1186/1758-907X-3-1
- miRNA Target
- Lock Nucleic Acid
- miRNA Inhibition
- miRNA Activity
- miRNA Sponge