Human Molecular Genetics

Human Molecular Genetics 2007 16(R1):R106-R113; doi:10.1093/hmg/ddm056

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miRNAs in cancer: approaches, aetiology, diagnostics and therapy

Cherie Blenkiron and Eric A. Miska^*

The Wellcome Trust/Cancer Research, UK Gurdon Institute and Department of Biochemistry, University of Cambridge, The Henry Wellcome Building of Cancer and Developmental Biology, Tennis Court Road, Cambridge CB2 1QN, UK

^* To whom correspondence should be addressed at: Tel: +44 1223767220; Fax: +44 1223767225; Email: eam29{at}cam.ac.uk

Received February 22, 2007; Accepted March 2, 2007

	ABSTRACT

TOP ABSTRACT INTRODUCTION OF WORMS AND FLIES MICRORNAs EXPRESSION PROFILING FUNCTIONAL STUDIES THE MIR-17-92 MIRNA CLUSTER MICRO-RNA BIOGENESIS GERMLINE MUTATIONS DIAGNOSTICS THERAPY CONCLUSIONS REFERENCES

 
MicroRNAs (miRNAs) are causing tremendous excitement in cancer research. MiRNAs are a large class of short non-coding RNAs that are found in many plants, animals and DNA viruses and often act to inhibit gene expression post-transcriptionally. Approximately 500 miRNA genes have been identified in the human genome. Their function is largely unknown, but data from worms, flies, fish and mice suggest that they have important roles in animal growth, development, homeostasis and disease. MiRNA expression profiles demonstrate that many miRNAs are deregulated in human cancers. MiRNAs have been shown to regulate oncogenes, tumour suppressors and a number of cancer-related genes controlling cell cycle, apoptosis, cell migration and angiogenesis. MiRNAs encoded by the mir-17-92 cluster have oncogenic potential and others may act as tumour suppressors. Some miRNAs and their target sites were found to be mutated in cancer. MiRNAs may have great diagnostic potential for human cancer and even miRNA-based cancer therapies may be on the horizon.

	INTRODUCTION

TOP ABSTRACT INTRODUCTION OF WORMS AND FLIES MICRORNAs EXPRESSION PROFILING FUNCTIONAL STUDIES THE MIR-17-92 MIRNA CLUSTER MICRO-RNA BIOGENESIS GERMLINE MUTATIONS DIAGNOSTICS THERAPY CONCLUSIONS REFERENCES

 
Over the last 10 years a small RNA revolution has swept biology. In 1998 interference RNA (RNAi) was discovered as an experimental tool by Andy Fire and Craig Mello, a finding that was awarded with the 2006 Nobel Prize for Physiology or Medicine (1). Although the biology of RNAi is still not understood, it has become a powerful experimental tool and is currently being developed for human gene therapy (2). During a similar timeframe and linked in some aspects to RNAi, microRNAs (miRNAs) were discovered as a new class of regulatory RNAs in animals, plants and viruses (3). miRNAs are transcribed from endogenous genes as long, primary RNA transcripts and are processed to their mature form: a single-stranded RNA with a length of approximately 22 nucleotides, indistinguishable from a small-interfering RNA (siRNA), the mediator of RNAi. In animals these long RNA precursors (pri-miRNAs) (4) are processed in the nucleus by the RNase III enzyme Drosha and Pasha/DGCR8 to form the approximately 70-base pre-miRNAs (5–9). Pre-miRNAs are exported from the nucleus by Exportin-5 (10), processed by the RNase III enzyme Dicer and incorporated into an Argonaute-containing silencing complex (RISC) (11). miRNAs are thought to regulate gene expression post-transcriptionally by forming Watson-Crick base pairs with target mRNAs. Their mechanism of action is still under debate, but likely includes inhibition of translation and mRNA degradation (12). In animals, most miRNAs are thought to form imperfect base pairs with their target mRNA(s) and these interaction sites are enriched in 3' un-translated regions (3'-UTRs) (3). As a consequence, miRNA target identification using computational approaches is non-trivial (13). The public database for miRNAs, miRBase release 9.1, currently lists 474 human microRNAs (14,15) and estimates for the total number of human microRNAs range from over one thousand (16) to tens of thousands (17). Although miRNAs have only been studied intensely for the last 5 years, important functions for miRNAs in animal development and, potentially, human disease, have already emerged (18).

This review focuses on the approaches and current experimental evidence for the involvement of miRNAs in the aetiology of human cancer and the potential for miRNAs in human cancer diagnostics and therapy.

	OF WORMS AND FLIES

TOP ABSTRACT INTRODUCTION OF WORMS AND FLIES MICRORNAs EXPRESSION PROFILING FUNCTIONAL STUDIES THE MIR-17-92 MIRNA CLUSTER MICRO-RNA BIOGENESIS GERMLINE MUTATIONS DIAGNOSTICS THERAPY CONCLUSIONS REFERENCES

 
Genetic analysis of the timing of development in the nematode Caenorhabditis elegans (19–21) led to the cloning of the first miRNA, lin-4 miRNA (22), and the identification of the first miRNA target, the lin-14 mRNA (23). The developmental timing or heterochronic pathway regulates stage-specific processes during C. elegans larval development (24). The lin-4 miRNA and the second miRNA to be identified, let-7 miRNA, control hypodermal cell-fate decisions during larval development (25). Three additional C. elegans let-7-like miRNAs, miR-48, miR-84 and miR-241 also act in the control of developmental timing (26,27). All five of these C. elegans miRNA genes are required for hypodermal stem cell lineages to undergo stage-specific terminal differentiation. As a consequence, loss-of-function mutations in any of these miRNAs lead to excess cellular proliferation. Based on these observations alone, lin-4 or let-7 family miRNAs may be thought of as candidate tumour suppressors. Subsequently, both miRNA families were found to be conserved in mammals (28,29) and the human let-7 miRNA has been directly implicated in cancer (30). The first microRNA whose function was studied in Drosophila is encoded by the bantam locus, which had previously been identified in a screen for de-regulated tissue growth (31,32). The bantam microRNA stimulates cell proliferation and reduces programmed cell death. Bantam directly regulates the pro-apoptotic gene hid. A second Drosophila microRNA, miR-14, also limits programmed cell death (33). Although no human orthologues of bantam or miR-14 have been identified yet, their role in tissue growth and apoptosis emphasize the potential roles for miRNAs in biological processes of relevance to human cancer.

	MICRORNAs EXPRESSION PROFILING

TOP ABSTRACT INTRODUCTION OF WORMS AND FLIES MICRORNAs EXPRESSION PROFILING FUNCTIONAL STUDIES THE MIR-17-92 MIRNA CLUSTER MICRO-RNA BIOGENESIS GERMLINE MUTATIONS DIAGNOSTICS THERAPY CONCLUSIONS REFERENCES

 
The first evidence for a direct link between miRNAs and human cancer came from the observation that two microRNA genes, mir-15 and mir-16 are located in a 30 kb region on chromosome 13 that had been found deleted in chronic lymphocytic leukaemia (CLL) cases, and that miR-15 and miR-16 expression is often reduced in CLL (34). A second study found that miR-143 and miR-145 expression levels were reduced in adenomatous and cancer stages of colorectal neoplasia (35). Both studies were focused on a small number of miRNAs and based on miRNA cloning and northern blotting approaches. Subsequent development of a number of miRNA microarray technologies coincided with an increased number of miRNA expression studies in human cancer (36–41). Crucially, quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR) for mature miRNAs have also become available for the analysis of small tissue samples and microarray miRNA validation (42,43). A current map of all miRNA loci implicated in at least two different human cancers through expression profiling lists 56 such loci (Fig. 1). However, the number of miRNAs implicated in human cancer by expression profiling will still increase likely substantially for two reasons: first, the recent availability of commercial miRNA profiling platforms will widen access to these tools and secondly, the number of known human miRNAs is still increasing, rendering even the most recently published expression studies incomplete. Some general themes from the expression profiles published to date are emerging. For example, a study of 334 primary human tumours and tissues interrogating the expression of 217 miRNAs revealed that miRNA expression profiles contain lineage-specific information, may classify even poorly differentiated tumours, and that many miRNAs are down-regulated in primary tumours when compared with normal tissues (40). The notion that a common set of miRNAs may be deregulated in many tumour types is also supported by the finding that a large number of miRNAs have been implicated in at least two distinct tumour types (Fig. 1). It is tempting to speculate that these miRNAs share anti-tumourigenic properties. It is unknown how miRNA expression in tumours may be de-regulated. The development of in situ approaches to directly visualize miRNAs in human tumour cells using oligonucleotide probes, which have been successful in plants, flies and fish (44–46), may help address the question if miRNA expression is altered stochastically or co-ordinately, is cell-specific or tumour-wide.

View larger version (26K): [in this window] [in a new window] [Download PowerPoint slide]   Figure 1. An miRNA cancer map. Chromosome positions of miRNAs implicated in human cancer are shown as coloured dots. Each dot represents a single miRNA or an miRNA cluster. Colours refer to tumour tissue type, as indicated. Only miRNAs, whose expression levels were found to be significantly altered in tumours versus normal tissues in at least two tissue types are shown. miRNAs identified in at least four different tumour types are also indicated by their name. Data were collated from the studies of primary human tumours of the colorectum (35,92,93), thyroid (60,94,95), breast (62,96), lung (97), liver (98), pancreas (99–101), uterus (52) and in chronic lymphocytic leukaemia (CLL) (37,64,102), glioblastoma (103) and neuroblastoma (104).

 

	FUNCTIONAL STUDIES

TOP ABSTRACT INTRODUCTION OF WORMS AND FLIES MICRORNAs EXPRESSION PROFILING FUNCTIONAL STUDIES THE MIR-17-92 MIRNA CLUSTER MICRO-RNA BIOGENESIS GERMLINE MUTATIONS DIAGNOSTICS THERAPY CONCLUSIONS REFERENCES

 
Two decades ago cell-based transformation assays identified the first human oncogenes and tumour suppressors (47). More recently, a cell-based screen identified miR-372 and miR-373 out of 197 miRNAs as putative oncogenes in a RAS co-operation assay (48). This study implicated miR-372 and miR-373 in the p53 pathway with the tumour suppressor LATS2 as a possible direct target and suggested a potential role for these miRNAs in testicular germ cell tumours (Table 1). A number of other studies have taken specific miRNAs identified in expression profiling experiments forward to carry out functional analyses. For example, miR-21 was found to be over-expressed in malignant cholangiocytes and miR-21 expression was found to down-regulate the tumour suppressor PTEN in these cells (49). In a separate study the microRNAs miR-20 and miR-106a were found to be able to regulate the tumour suppressors TGFBR2 and RB, respectively (50). All of the above, and work on the miR-17 to -92 cluster of miRNAs that will be discussed in the next section, suggest that a number of miRNAs may have oncogenic potential. However, several miRNAs have been proposed to act as tumour suppressors. The first of these included members of the let-7 family, which were reported to regulate the expression of the RAS oncogene in C. elegans and in human cells (30). The same study found let-7 to be down-regulated in lung tumours and its expression anti-correlated with that of RAS. This observation was particularly intriguing given the functional studies of the let-7 miRNA in C. elegans. The let-7 family was subsequently found to be de-regulated in a large number of tumour types (Fig. 1) and the oncogenes HMGA2 and FOS have been added to its list of putative targets (51–53). Other oncogenes that may be targeted directly by miRNAs include AIB1, BCL2, BCL6, E2F3, KIT and TCL1 (54–62). Interestingly, miR-21 was shown to be able to regulate the oncogene PTEN in cholangiocytes (49) and the tumour suppressor BCL2 in the breast cancer cell line MCF-7 (57), suggesting that miR-21 may act as a tumour suppressor or oncogene depending on cellular context. All cancer-related genes that may be targeted by one or more miRNAs are listed in Table 1.

View this table: [in this window] [in a new window]   Table 1. miRNAs that may regulate cancer-related genes

 

	THE MIR-17-92 MIRNA CLUSTER

TOP ABSTRACT INTRODUCTION OF WORMS AND FLIES MICRORNAs EXPRESSION PROFILING FUNCTIONAL STUDIES THE MIR-17-92 MIRNA CLUSTER MICRO-RNA BIOGENESIS GERMLINE MUTATIONS DIAGNOSTICS THERAPY CONCLUSIONS REFERENCES

 
If the let-7 miRNA is the best-studied candidate tumour suppressor miRNA, the mir-17-92 miRNA polycistron is the best-studied miRNA with oncogenic potential and was named ‘OncomiR-1’. The mir-17-92 cluster (c13orf25) is part of a region on chromosome 13 amplified in malignant lymphoma including B-cell lymphoma (63). Using a well-established mouse model of B-cell lymphoma in which haematopoietic stem cells over-expressing the oncogenic transcription factor Myc are used to generate mosaic animals it was demonstrated that mice mosaic for cells over-expressing Myc and the mir-17-92 cluster developed tumours earlier than mice with cells over-expressing Myc alone (64). Furthermore, Myc and mir-17-92 cluster-induced tumours were more aggressive with higher mitotic indices than Myc-only induced tumours (64). An independent study demonstrated that Myc directly binds to and regulates the transcription of the mir-17-92 cluster in cell culture and that the miRNAs of this cluster regulate the expression of E2f1 (65). These two studies suggested a complex network of regulation whereby MYC, which is a positive regulator of E2F1 transcription, dampens the E2F1 response through the miRNAs of the mir-17-92 cluster (Fig. 2). However, the picture is likely more complex involving several E2F proteins (E2F1, E2F2, E2F3), feedback loops from E2F to MYC and from E2F to the mir-17-92 cluster and affects angiogenesis and tumour metastases by targeting TSP1, CTGF and TGFBR2 (50,62,65–71).

View larger version (15K): [in this window] [in a new window] [Download PowerPoint slide]   Figure 2. Interaction map of the oncogenic miR-17-92 cluster on chromosome 13 q13.3. Proteins in red and green are products of known human oncogenes and tumour suppressors, respectively (50,62,65–71).

 

	MICRO-RNA BIOGENESIS

TOP ABSTRACT INTRODUCTION OF WORMS AND FLIES MICRORNAs EXPRESSION PROFILING FUNCTIONAL STUDIES THE MIR-17-92 MIRNA CLUSTER MICRO-RNA BIOGENESIS GERMLINE MUTATIONS DIAGNOSTICS THERAPY CONCLUSIONS REFERENCES

 
The de-regulation of many miRNAs in human cancer raises the question of how these changes are orchestrated. The previous section possibly offers a simple explanation for the mir-17-92 cluster, which is directly regulated by the oncogene Myc (65). In some cases, changes in miRNA expression may therefore reflect changes in the upstream transcriptional network. In the case of mir-127, transcription appears to be regulated at the level of histone acetylation and DNA methylation (56). Recently, similar observations were made for the mir-124a and the let-7a-3 loci (72,73). However, this may not be a general phenomenon (74). In contrast, miRNA expression may also be regulated post-transcriptionally. This possibility was first noted, when it was shown that the let-7 pre-miRNA in sea urchins is present throughout development, whereas the mature form is stage-specific (28). Similar developmental regulation of miRNA processing was observed in the mouse (75). Moreover, the mouse pre-miRNA miR-138-2 was found to be expressed ubiquitously, but only processed to its mature form in specific tissues (76). As most miRNA expression profiles are focussed on the mature miRNA, deregulation in cancer may be a reflection of changes in post-transcriptional processing at the level of the pri-miRNA or pre-miRNA. Indeed, in mouse embryos let-7 family pri-miRNAs accumulate prior to processing by the Drosha (77). The same study also claimed that post-transcriptional regulation of miRNAs in cancer is common as a cross-platform analysis of miRNA and mRNA expression profiles of primary human tumours lacked correlation (40,77,78). The mechanism(s) controlling differential miRNA processing is currently unknown, but may prove important for understanding the roles of miRNAs in cancer in future. However, given that many miRNAs are deregulated in cancer, it is possible that alterations in the core biogenesis machinery contribute to cancer. Indeed, elevated DICER levels have been reported in prostate adenocarcinoma (79) and Burkitt's lymphoma (80) and reduced DICER levels have been reported in lung cancer (81).

	GERMLINE MUTATIONS

TOP ABSTRACT INTRODUCTION OF WORMS AND FLIES MICRORNAs EXPRESSION PROFILING FUNCTIONAL STUDIES THE MIR-17-92 MIRNA CLUSTER MICRO-RNA BIOGENESIS GERMLINE MUTATIONS DIAGNOSTICS THERAPY CONCLUSIONS REFERENCES

 
Given the data implicating miRNAs in cancer reviewed here, one might expect germline mutations in miRNAs to be involved in cancer pre-disposition. Indeed, single nucleotide polymorphisms (SNPs) in the primary transcripts of miR-15a and mIR-16-1 may be linked to CLL (82). But the net should be cast much wider to include miRNA targets. Our current understanding of miRNA interaction with target mRNAs suggests that a single 3'-UTR mutation might make or break the miRNA interaction (13). The importance of mutations in miRNA binding site for inheritable traits has already been demonstrated in the case of Texel sheep, where a quantitative trait locus maps to a mutation in the 3'-UTR of the muscle-specific gene GDF8, which renders it a target for the miRNAs miR-1 and miR-206 (83). miRNA target site mutations have also been shown to be of potential importance for human disease as a mutation in a putative miR-189 binding-site in human SLITRK1 may be linked to Tourette's syndrome (84). Interestingly, SNPs in the binding sites for the miRNAs miR-146, miR-221 and miR-222 in the oncogene KIT may be linked to papillary thyroid carcinoma (60). However, a recent study identified a number of SNPs in primary miRNA sequences, one in the pre-miRNA for miR-26-a1, and none in mature miRNAs in a panel of 91 human cancer cell lines (74). None of the miRNA-associated SNPs resulted in changes in miRNA expression or processing (74).

	DIAGNOSTICS

TOP ABSTRACT INTRODUCTION OF WORMS AND FLIES MICRORNAs EXPRESSION PROFILING FUNCTIONAL STUDIES THE MIR-17-92 MIRNA CLUSTER MICRO-RNA BIOGENESIS GERMLINE MUTATIONS DIAGNOSTICS THERAPY CONCLUSIONS REFERENCES

 
The body of expression data for miRNAs in cancer available to date suggests that miRNAs may have diagnostic potential. However, while initial expression studies focused on comparing normal tissues to tumours, to gauge diagnostic potential it will be more important to correlate miRNA expression with tumour subtypes or clinical parameters. A number of studies show promise in this regard. For example, a qRT-PCR-based study identified subsets of miRNAs that distinguish ErbB2-positive from ErbB2-negative and ER-positive from ER-negative breast cancers from biopsies (85). If miRNA expression data can be used to build discriminators with clinical value, miRNAs have clear advantages over mRNAs: they are long-lived in vivo (86) and very stable in vitro.

	THERAPY

TOP ABSTRACT INTRODUCTION OF WORMS AND FLIES MICRORNAs EXPRESSION PROFILING FUNCTIONAL STUDIES THE MIR-17-92 MIRNA CLUSTER MICRO-RNA BIOGENESIS GERMLINE MUTATIONS DIAGNOSTICS THERAPY CONCLUSIONS REFERENCES

 
Given the emerging evidence of miRNAs with oncogenic or tumour suppressor activities, it is important to seek routes to interfere with miRNAs and to develop these as novel cancer therapies. In the case of the oncogenic mir-17-92 cluster it might therefore be of interest to specifically knockdown the expression of all miRNAs derived from this cluster. In mammalian cell culture, 2-O-methyl oligoribonucleotides (2-O-Me-RNA) have been used to specifically down-regulate miRNAs (87). Cell-permeable forms of these 2-O-Me-RNAs, called ‘antagomirs’ were successful in down-regulating several mouse miRNAs in a number of mouse tissues following intravenous injection in vivo (88). It remains an open question whether these or similar strategies will allow us to deliver anti-miRNA cancer therapies. One complication that may make the task more difficult is the potential redundancy of miRNAs: would targeting mir-17 be sufficient or would all miRNAs of the mir-17-92 cluster have to be targeted? In contrast, for miRNAs that act as tumour suppressors it may be of interest to develop in vivo expression systems. As miRNAs are chemically identical to siRNAs ongoing efforts to deliver siRNAs as RNAi-based anti-cancer therapies, if successful, should provide suitable vehicles for the delivery of miRNAs (2). In fact, some methods of siRNA delivery make use of the miRNA biogenesis pathway to increase efficiency (2). Even if the delivery problem may be solved, one major obstacle to the efficacy of siRNA- or miRNA-based therapies may be the potential of off-target effects (89,90). Finally, inhibiting miRNA expression globally by interfering with their biogenesis may have therapeutic potential just as inhibiting global chromatin-modifying enzymes such as histone deacetylases (HDACs) is proving effective in some types of cancer (91).

	CONCLUSIONS

TOP ABSTRACT INTRODUCTION OF WORMS AND FLIES MICRORNAs EXPRESSION PROFILING FUNCTIONAL STUDIES THE MIR-17-92 MIRNA CLUSTER MICRO-RNA BIOGENESIS GERMLINE MUTATIONS DIAGNOSTICS THERAPY CONCLUSIONS REFERENCES

 
The last 6 years have demonstrated the importance of miRNAs in biology. The evidence for roles of miRNAs in human disease, in particular cancer, is overwhelming. Diagnostic potentials for miRNAs have been identified and we expect that clinical diagnostic trials will test their efficacy soon. There are clear opportunities for miRNA-based anti-cancer therapeutics. Although initially in the shadow of RNAi, miRNAs have become the brightest star of the small RNA revolution.

	ACKNOWLEDGEMENTS

 
We thank Ines Alvarez-Garcia for help with the manuscript. E.A.M. is a Cancer Research UK Programme Grant Holder (C13474/A4613).

Conflict of Interest statement. None declared.

	REFERENCES

TOP ABSTRACT INTRODUCTION OF WORMS AND FLIES MICRORNAs EXPRESSION PROFILING FUNCTIONAL STUDIES THE MIR-17-92 MIRNA CLUSTER MICRO-RNA BIOGENESIS GERMLINE MUTATIONS DIAGNOSTICS THERAPY CONCLUSIONS REFERENCES

 

1. Fire A., Xu S., Montgomery M.K., Kostas S.A., Driver S.E., Mello C.C. Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans. Nature (1998) 391:806–811.[CrossRef][Medline]

2. Bumcrot D., Manoharan M., Koteliansky V., Sah D.W. RNAi therapeutics: a potential new class of pharmaceutical drugs. Nat. Chem. Biol. (2006) 2:711–719.[CrossRef][Web of Science][Medline]

3. Bartel D.P. MicroRNAs: genomics, biogenesis, mechanism, and function. Cell (2004) 116:281–297.[CrossRef][Web of Science][Medline]

4. Kim V.N. MicroRNA biogenesis: coordinated cropping and dicing. Nat. Rev. Mol. Cell. Biol. (2005) 6:376–385.[CrossRef][Web of Science][Medline]

5. Lee Y., Ahn C., Han J., Choi H., Kim J., Yim J., Lee J., Provost P., Radmark O., Kim S., et al. The nuclear RNase III Drosha initiates microRNA processing. Nature (2003) 425:415–419.[CrossRef][Medline]

6. Landthaler M., Yalcin A., Tuschl T. The human DiGeorge syndrome critical region gene 8 and its D. melanogaster homolog are required for miRNA biogenesis. Curr. Biol. (2004) 14:2162–2167.[CrossRef][Web of Science][Medline]

7. Han J., Lee Y., Yeom K.H., Kim Y.K., Jin H., Kim V.N. The Drosha–DGCR8 complex in primary microRNA processing. Genes Dev. (2004) 18:3016–3027.[Abstract/Free Full Text]

8. Gregory R.I., Yan K.P., Amuthan G., Chendrimada T., Doratotaj B., Cooch N., Shiekhattar R. The microprocessor complex mediates the genesis of microRNAs. Nature (2004) 432:235–240.[CrossRef][Medline]

9. Denli A.M., Tops B.B., Plasterk R.H., Ketting R.F., Hannon G.J. Processing of primary microRNAs by the microprocessor complex. Nature (2004) 432:231–235.[CrossRef][Medline]

10. Lund E., Guttinger S., Calado A., Dahlberg J.E., Kutay U. Nuclear export of microRNA precursors. Science (2004) 303:95–98.[Abstract/Free Full Text]

11. Du T., Zamore P.D. microPrimer: the biogenesis and function of microRNA. Development (2005) 132:4645–4652.[Abstract/Free Full Text]

12. Jackson R.J., Standart N. How do microRNAs regulate gene expression? Sci STKE (2007) 367:re1.

13. John B., Sander C., Marks D.S. Prediction of human microRNA targets. Methods Mol. Biol. (2006) 342:101–113.[Medline]

14. Griffiths-Jones S. The microRNA registry. Nucleic Acids Res. (2004) 32:D109–D111.[Abstract/Free Full Text]

15. Griffiths-Jones S., Grocock R.J., van Dongen S., Bateman A., Enright A.J. miRBase: microRNA sequences, targets and gene nomenclature. Nucleic Acids Res. (2006) 34:D140–D144.[Abstract/Free Full Text]

16. Berezikov E., Guryev V., van de Belt J., Wienholds E., Plasterk R.H., Cuppen E. Phylogenetic shadowing and computational identification of human microRNA genes. Cell (2005) 120:21–24.[CrossRef][Web of Science][Medline]

17. Miranda K.C., Huynh T., Tay Y., Ang Y.S., Tam W.L., Thomson A.M., Lim B., Rigoutsos I. A pattern-based method for the identification of microRNA binding sites and their corresponding heteroduplexes. Cell (2006) 126:1203–1217.[CrossRef][Web of Science][Medline]

18. Alvarez-Garcia I., Miska E.A. MicroRNA functions in animal development and human disease. Development (2005) 132:4653–4662.[Abstract/Free Full Text]

19. Horvitz H.R., Sulston J.E. Isolation and genetic characterization of cell-lineage mutants of the nematode Caenorhabditis elegans. Genetics (1980) 96:435–454.[Abstract/Free Full Text]

20. Ambros V., Moss E.G. Heterochronic genes and the temporal control of C. elegans development. Trends Genet. (1994) 10:123–127.[CrossRef][Web of Science][Medline]

21. Chalfie M., Horvitz H.R., Sulston J.E. Mutations that lead to reiterations in the cell lineages of C. elegans. Cell (1981) 24:59–69.[CrossRef][Web of Science][Medline]

22. Lee R.C., Feinbaum R.L., Ambros V. The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14. Cell (1993) 75:843–854.[CrossRef][Web of Science][Medline]

23. Wightman B., Ha I., Ruvkun G. Post-transcriptional regulation of the heterochronic gene lin-14 by lin-4 mediates temporal pattern formation in C. elegans. Cell (1993) 75:855–862.[CrossRef][Web of Science][Medline]

24. Rougvie A.E. Intrinsic and extrinsic regulators of developmental timing: from miRNAs to nutritional cues. Development (2005) 132:3787–3798.[Abstract/Free Full Text]

25. Reinhart B.J., Slack F.J., Basson M., Pasquinelli A.E., Bettinger J.C., Rougvie A.E., Horvitz H.R., Ruvkun G. The 21-nucleotide let-7 RNA regulates developmental timing in Caenorhabditis elegans. Nature (2000) 403:901–906.[CrossRef][Medline]

26. Abbott A.L., Alvarez-Saavedra E., Miska E.A., Lau N.C., Bartel D.P., Horvitz H.R., 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.[CrossRef][Web of Science][Medline]

27. Li M., Jones-Rhoades M.W., Lau N.C., Bartel D.P., Rougvie A.E. Regulatory mutations of mir-48, a C. elegans let-7 family MicroRNA, cause developmental timing defects. Dev. Cell (2005) 9:415–422.[CrossRef][Web of Science][Medline]

28. Pasquinelli A.E., Reinhart B.J., Slack F., Martindale M.Q., Kuroda M.I., Maller B., Hayward D.C., Ball E.E., Degnan B., Muller P., et al. Conservation of the sequence and temporal expression of let-7 heterochronic regulatory RNA. Nature (2000) 408:86–89.[CrossRef][Medline]

29. Lagos-Quintana M., Rauhut R., Yalcin A., Meyer J., Lendeckel W., Tuschl T. Identification of tissue-specific microRNAs from mouse. Curr. Biol. (2002) 12:735–739.[CrossRef][Web of Science][Medline]

30. Johnson S.M., Grosshans H., Shingara J., Byrom M., Jarvis R., Cheng A., Labourier E., Reinert K.L., Brown D., Slack F.J. RAS is regulated by the let-7 microRNA family. Cell (2005) 120:635–647.[CrossRef][Web of Science][Medline]

31. Hipfner D.R., Weigmann K., Cohen S.M. The bantam gene regulates Drosophila growth. Genetics (2002) 161:1527–1537.[Abstract/Free Full Text]

32. Brennecke J., Hipfner D.R., Stark A., Russell R.B., Cohen S.M. Bantam encodes a developmentally regulated microRNA that controls cell proliferation and regulates the proapoptotic gene hid in Drosophila. Cell (2003) 113:25–36.[CrossRef][Web of Science][Medline]

33. Xu P., Vernooy S.Y., Guo M., Hay B.A. The Drosophila microRNA mir-14 suppresses cell death and is required for normal fat metabolism. Curr. Biol. (2003) 13:790–795.[CrossRef][Web of Science][Medline]

34. Calin G.A., Dumitru C.D., Shimizu M., Bichi R., Zupo S., Noch E., Aldler H., Rattan S., Keating M., Rai K., et al. Frequent deletions and down-regulation of micro-RNA genes miR15 and miR16 at 13q14 in chronic lymphocytic leukemia. Proc. Natl Acad. Sci. USA (2002) 99:15524–15529.[Abstract/Free Full Text]

35. Michael M.Z., SM O.C., van Holst Pellekaan N.G., Young G.P., James R.J. Reduced accumulation of specific microRNAs in colorectal neoplasia. Mol. Cancer Res. (2003) 1:882–891.[Abstract/Free Full Text]

36. Krichevsky A.M., King K.S., Donahue C.P., Khrapko K., Kosik K.S. A microRNA array reveals extensive regulation of microRNAs during brain development. RNA (2003) 9:1274–1281.[Abstract/Free Full Text]

37. Calin G.A., Liu C.G., Sevignani C., Ferracin M., Felli N., Dumitru C.D., Shimizu M., Cimmino A., Zupo S., Dono M., et al. MicroRNA profiling reveals distinct signatures in B cell chronic lymphocytic leukemias. Proc. Natl Acad. Sci. USA (2004) 101:11755–11760.[Abstract/Free Full Text]

38. Miska E.A., Alvarez-Saavedra E., Townsend M., Yoshii A., Sestan N., Rakic P., Constantine-Paton M., Horvitz H.R. Microarray analysis of microRNA expression in the developing mammalian brain. Genome Biol. (2004) 5:R68.[CrossRef][Medline]

39. Thomson J.M., Parker J., Perou C.M., Hammond S.M. A custom microarray platform for analysis of microRNA gene expression. Nat. Methods (2004) 1:47–53.[CrossRef][Web of Science][Medline]

40. Lu J., Getz G., Miska E.A., Alvarez-Saavedra E., Lamb J., Peck D., Sweet-Codero A., Ebert B.L., Mak R.H., Ferrando A.A., et al. MicroRNA expression profiles classify human cancers. Nature (2005) 435:834–838.[CrossRef][Medline]

41. Liu C.G., Calin G.A., Meloon B., Gamliel N., Sevignani C., Ferracin M., Dumitru C.D., Shimizu M., Zupo S., Dono M., et al. An oligonucleotide microchip for genome-wide microRNA profiling in human and mouse tissues. Proc. Natl Acad. Sci. USA (2004) 101:9740–9744.[Abstract/Free Full Text]

42. Shi R., Chiang V.L. Facile means for quantifying microRNA expression by real-time PCR. Biotechniques (2005) 39:519–525.[Web of Science][Medline]

43. Tang F., Hajkova P., Barton S.C., Lao K., Surani M.A. MicroRNA expression profiling of single whole embryonic stem cells. Nucleic Acids Res. (2006) 34:e9.[Abstract/Free Full Text]

44. Kidner C.A., Martienssen R.A. Spatially restricted microRNA directs leaf polarity through ARGONAUTE1. Nature (2004) 428:81–84.[CrossRef][Medline]

45. Sokol N.S., 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.[Abstract/Free Full Text]

46. Wienholds E., Kloosterman W.P., Miska E., Alvarez-Saavedra E., Berezikov E., de Bruijn E., Horvitz H.R., Kauppinen S., Plasterk R.H. MicroRNA expression in zebrafish embryonic development. Science (2005) 309:310–311.[Abstract/Free Full Text]

47. Friend S.H., Dryia T.P., Weinberg R.A. Oncogenes and tumor-suppressing genes. N. Engl. J. Med. (1988) 318:618–622.[Web of Science][Medline]

48. Voorhoeve P.M., le Sage C., Schrier M., Gillis A.J., Stoop H., Nagel R., Liu Y.P., van Duijse J., Drost J., Griekspoor A., et al. A genetic screen implicates miRNA-372 and miRNA-373 as oncogenes in testicular germ cell tumors. Cell (2006) 124:1169–1181.[CrossRef][Web of Science][Medline]

49. Meng F., Henson R., Lang M., Wehbe H., Maheshwari S., Mendell J.T., Jiang J., Schmittgen T.D., Patel T. Involvement of human micro-RNA in growth and response to chemotherapy in human cholangiocarcinoma cell lines. Gastroenterology (2006) 130:2113–2129.[CrossRef][Web of Science][Medline]

50. Volinia S., Calin G.A., Liu C.G., Ambs S., Cimmino A., Petrocca F., Visone R., Iorio M., Roldo C., Ferracin M., et al. A microRNA expression signature of human solid tumors defines cancer gene targets. Proc. Natl Acad. Sci. USA (2006) 103:2257–2261.[Abstract/Free Full Text]

51. Lee H.J., Palkovits M., Young W.S. III. miR-7b, a microRNA up-regulated in the hypothalamus after chronic hyperosmolar stimulation, inhibits Fos translation. Proc. Natl Acad. Sci. USA (2006) 103:15669–15674.[Abstract/Free Full Text]

52. Wang T., Zhang X., Obijuru L., Laser J., Aris V., Lee P., Mittal K., Soteropoulos P., Wei J.J. A micro-RNA signature associated with race, tumor size, and target gene activity in human uterine leiomyomas. Genes Chrom. Cancer (2007) 46:336–347.[CrossRef][Web of Science][Medline]

53. Hebert C., Norris K., Scheper M.A., Nikitakis N., Sauk J.J. High mobility group A2 is a target for miRNA-98 in head and neck squamous cell carcinoma. Mol. Cancer (2007) 6:5.[CrossRef][Medline]

54. Welch C., Chen Y., Stallings R.L. MicroRNA-34a functions as a potential tumor suppressor by inducing apoptosis in neuroblastoma cells. In: Oncogene (2007) Epub ahead of print 12 Feb 2007, doi: 10.1038/sj.onc.1210293.

55. Pekarsky Y., Santanam U., Cimmino A., Palamarchuk A., Efanov A., Maximov V., Volinia S., Alder H., Liu C.G., Rassenti L., et al. Tcl1 expression in chronic lymphocytic leukemia is regulated by miR-29 and miR-181. Cancer Res. (2006) 66:11590–11593.[Abstract/Free Full Text]

56. Saito Y., Liang G., Egger G., Friedman J.M., Chuang J.C., Coetzee G.A., Jones P.A. Specific activation of microRNA-127 with downregulation of the proto-oncogene BCL6 by chromatin-modifying drugs in human cancer cells. Cancer Cell (2006) 9:435–443.[CrossRef][Web of Science][Medline]

57. Si M.L., Zhu S., Wu H., Lu Z., Wu F., Mo Y.Y. miR-21-mediated tumor growth. In: Oncogene (2006) Epub ahead of print 30 Oct 2006, doi: 10.1038/sj.onc.1210083.

58. Cimmino A., Calin G.A., Fabbri M., Iorio M.V., Ferracin M., Shimizu M., Wojcik S.E., Aqeilan R.I., Zupo S., Dono M., et al. miR-15 and miR-16 induce apoptosis by targeting BCL2. Proc. Natl Acad. Sci. USA (2005) 102:13944–13949.[Abstract/Free Full Text]

59. Felli N., Fontana L., Pelosi E., Botta R., Bonci D., Facchiano F., Liuzzi F., Lulli V., Morsilli O., Santoro S., et al. MicroRNAs 221 and 222 inhibit normal erythropoiesis and erythroleukemic cell growth via kit receptor down-modulation. Proc. Natl Acad. Sci. USA (2005) 102:18081–18086.[Abstract/Free Full Text]

60. He H., Jazdzewski K., Li W., Liyanarachchi S., Nagy R., Volinia S., Calin G.A., Liu C.G., Franssila K., Suster S., et al. The role of microRNA genes in papillary thyroid carcinoma. Proc. Natl Acad. Sci. USA (2005) 102:19075–19080.[Abstract/Free Full Text]

61. Poliseno L., Tuccoli A., Mariani L., Evangelista M., Citti L., Woods K., Mercatanti A., Hammond S., Rainaldi G. MicroRNAs modulate the angiogenic properties of HUVECs. Blood (2006) 108:3068–3071.[Abstract/Free Full Text]

62. Hossain A., Kuo M.T., Saunders G.F. Mir-17-5p regulates breast cancer cell proliferation by inhibiting translation of AIB1 mRNA. Mol. Cell. Biol. (2006) 26:8191–8201.[Abstract/Free Full Text]

63. Ota A., Tagawa H., Karnan S., Tsuzuki S., Karpas A., Kira S., Yoshida Y., Seto M. Identification and characterization of a novel gene, C13orf25, as a target for 13q31-q32 amplification in malignant lymphoma. Cancer Res. (2004) 64:3087–3095.[Abstract/Free Full Text]

64. He L., Thomson J.M., Hemann M.T., Hernando-Monge E., Mu D., Goodson S., Powers S., Cordon-Cardo C., Lowe S.W., Hannon G.J., et al. A microRNA polycistron as a potential human oncogene. Nature (2005) 435:828–833.[CrossRef][Medline]

65. O'Donnell K.A., Wentzel E.A., Zeller K.I., Dang C.V., Mendell J.T. c-Myc-regulated microRNAs modulate E2F1 expression. Nature (2005) 435:839–843.[CrossRef][Medline]

66. Wang C.L., Wang B.B., Bartha G., Li L., Channa N., Klinger M., Killeen N., Wabl M. Activation of an oncogenic microRNA cistron by provirus integration. Proc. Natl Acad. Sci. USA (2006) 103:18680–18684.[Abstract/Free Full Text]

67. Woods K., Thomson J.M., Hammond S.M. Direct regulation of an oncogenic micro-RNA cluster by E2F transcription factors. In: J. Biol. Chem. (2007) 282:2130–2134.[Abstract/Free Full Text]

68. Venturini L., Battmer K., Castoldi M., Schultheis B., Hochhaus A., Muckenthaler M.U., Ganser A., Eder M., Scherr M. Expression of the miR-17-92 polycistron in chronic myeloid leukemia (CML) CD34+ cells. In: Blood (2007) Epub ahead of print 6 Feb 2007, doi: 10.1182/blood-2006-09-045104.

69. Dews M., Homayouni A., Yu D., Murphy D., Sevignani C., Wentzel E., Furth E.E., Lee W.M., Enders G.H., Mendell J.T., et al. Augmentation of tumor angiogenesis by a Myc-activated microRNA cluster. Nat. Genet. (2006) 38:1060–1065.[CrossRef][Web of Science][Medline]

70. Sylvestre Y., De Guire V., Querido E., Mukhopadhyay U.K., Bourdeau V., Major F., Ferbeyre G., Chartrand P. An E2F/miR-20a autoregulatory feedback loop. J. Biol. Chem. (2007) 282:2135–2143.[Abstract/Free Full Text]

71. Hayashita Y., Osada H., Tatematsu Y., Yamada H., Yanagisawa K., Tomida S., Yatabe Y., Kawahara K., Sekido Y., Takahashi T. A polycistronic microRNA cluster, miR-17-92, is overexpressed in human lung cancers and enhances cell proliferation. Cancer Res. (2005) 65:9628–9632.[Abstract/Free Full Text]

72. Brueckner B., Stresemann C., Kuner R., Mund C., Musch T., Meister M., Sultmann H., Lyko F. The human let-7a-3 locus contains an epigenetically regulated microRNA gene with oncogenic function. Cancer Res. (2007) 67:1419–1423.[Abstract/Free Full Text]

73. Lujambio A., Ropero S., Ballestar E., Fraga M.F., Cerrato C., Setien F., Casado S., Suarez-Gauthier A., Sanchez-Cespedes M., Gitt A., et al. Genetic unmasking of an epigenetically silenced microRNA in human cancer cells. Cancer Res. (2007) 67:1424–1429.[Abstract/Free Full Text]

74. Diederichs S., Haber D.A. Sequence variations of microRNAs in human cancer: alterations in predicted secondary structure do not affect processing. Cancer Res. (2006) 66:6097–6104.[Abstract/Free Full Text]

75. Schulman B.R., Esquela-Kerscher A., Slack F.J. Reciprocal expression of lin-41 and the microRNAs let-7 and mir-125 during mouse embryogenesis. Dev. Dyn. (2005) 234:1046–1054.[CrossRef][Web of Science][Medline]

76. Obernosterer G., Leuschner P.J., Alenius M., Martinez J. Post-transcriptional regulation of microRNA expression. RNA (2006) 12:1161–1167.[Abstract/Free Full Text]

77. Thomson J.M., Newman M., Parker J.S., Morin-Kensicki E.M., Wright T., Hammond S.M. Extensive post-transcriptional regulation of microRNAs and its implications for cancer. Genes Dev. (2006) 20:2202–2207.[Abstract/Free Full Text]

78. Ramaswamy S., Tamayo P., Rifkin R., Mukherjee S., Yeang C.H., Angelo M., Ladd C., Reich M., Latulippe E., Mesirov J.P., et al. Multiclass cancer diagnosis using tumor gene expression signatures. Proc. Natl Acad. Sci. USA (2001) 98:15149–15154.[Abstract/Free Full Text]

79. Chiosea S., Jelezcova E., Chandran U., Acquafondata M., McHale T., Sobol R.W., Dhir R. Up-regulation of dicer, a component of the MicroRNA machinery, in prostate adenocarcinoma. Am. J. Pathol. (2006) 169:1812–1820.[Abstract/Free Full Text]

80. Kaul D., Sikand K. Defective RNA-mediated c-myc gene silencing pathway in Burkitt's lymphoma. Biochem. Biophys. Res. Commun. (2004) 313:552–554.[CrossRef][Web of Science][Medline]

81. Karube Y., Tanaka H., Osada H., Tomida S., Tatematsu Y., Yanagisawa K., Yatabe Y., Takamizawa J., Miyoshi S., Mitsudomi T., et al. Reduced expression of Dicer associated with poor prognosis in lung cancer patients. Cancer Sci. (2005) 96:111–115.[CrossRef][Medline]

82. Calin G.A., Ferracin M., Cimmino A., Di Leva G., Shimizu M., Wojcik S.E., Iorio M.V., Visone R., Sever N.I., Fabbri M., et al. A microRNA signature associated with prognosis and progression in chronic lymphocytic leukemia. N. Engl. J. Med. (2005) 353:1793–1801.[Abstract/Free Full Text]

83. Clop A., Marcq F., Takeda H., Pirottin D., Tordoir X., Bibe B., Bouix J., Caiment F., Elsen J.M., Eychenne F., et al. A mutation creating a potential illegitimate microRNA target site in the myostatin gene affects muscularity in sheep. Nat. Genet. (2006) 38:813–818.[CrossRef][Web of Science][Medline]

84. Abelson J.F., Kwan K.Y., O'Roak B.J., Baek D.Y., Stillman A.A., Morgan T.M., Mathews C.A., Pauls D.L., Rasin M.R., Gunel M., et al. Sequence variants in SLITRK1 are associated with Tourette's syndrome. Science (2005) 310:317–320.[Abstract/Free Full Text]

85. Mattie M.D., Benz C.C., Bowers J., Sensinger K., Wong L., Scott G.K., Fedele V., Ginzinger D., Getts R., Haqq C. Optimized high-throughput microRNA expression profiling provides novel biomarker assessment of clinical prostate and breast cancer biopsies. Mol. Cancer (2006) 5:24.[CrossRef][Medline]

86. Lim L.P., Lau N.C., Garrett-Engele P., Grimson A., Schelter J.M., Castle J., Bartel D.P., Linsley P.S., Johnson J.M. Microarray analysis shows that some microRNAs downregulate large numbers of target mRNAs. Nature (2005) 433:769–773.[CrossRef][Medline]

87. Hutvagner G., Simard M.J., Mello C.C., Zamore P.D. Sequence-specific inhibition of small RNA function. PLoS Biol. (2004) 2:e98.[CrossRef][Medline]

88. Krutzfeldt J., Rajewsky N., Braich R., Rajeev K.G., Tuschl T., Manoharan M., Stoffel M. Silencing of microRNAs in vivo with ‘antagomirs’. Nature (2005) 438:685–689.[CrossRef][Medline]

89. Jackson A.L., Bartz S.R., Schelter J., Kobayashi S.V., Burchard J., Mao M., Li B., Cavet G., Linsley P.S. Expression profiling reveals off-target gene regulation by RNAi. Nat. Biotechnol. (2003) 21:635–637.[CrossRef][Web of Science][Medline]

90. Jackson A.L., Burchard J., Schelter J., Chau B.N., Cleary M., Lim L., Linsley P.S. Widespread siRNA ‘off-target’ transcript silencing mediated by seed region sequence complementarity. RNA (2006) 12:1179–1187.[Abstract/Free Full Text]

91. Carey N., La Thangue N.B. Histone deacetylase inhibitors: gathering pace. Curr. Opin. Pharmacol. (2006) 6:369–375.[CrossRef][Web of Science][Medline]

92. Bandres E., Cubedo E., Agirre X., Malumbres R., Zarate R., Ramirez N., Abajo A., Navarro A., Moreno I., Monzo M., et al. Identification by real-time PCR of 13 mature microRNAs differentially expressed in colorectal cancer and non-tumoral tissues. Mol. Cancer (2006) 5:29.[CrossRef][Web of Science][Medline]

93. Akao Y., Nakagawa Y., Naoe T. let-7 microRNA functions as a potential growth suppressor in human colon cancer cells. Biol. Pharm. Bull. (2006) 29:903–906.[CrossRef][Web of Science][Medline]

94. Pallante P., Visone R., Ferracin M., Ferraro A., Berlingieri M.T., Troncone G., Chiappetta G., Liu C.G., Santoro M., Negrini M., et al. MicroRNA deregulation in human thyroid papillary carcinomas. Endocr. Relat. Cancer (2006) 13:497–508.[Abstract/Free Full Text]

95. Weber F., Teresi R.E., Broelsch C.E., Frilling A., Eng C. A limited set of human microRNA is deregulated in follicular thyroid carcinoma. J. Clin. Endocrinol. Metab. (2006) 91:3584–3591.[Abstract/Free Full Text]

96. Iorio M.V., Ferracin M., Liu C.G., Veronese A., Spizzo R., Sabbioni S., Magri E., Pedriali M., Fabbri M., Campiglio M., et al. MicroRNA gene expression deregulation in human breast cancer. Cancer Res. (2005) 65:7065–7070.[Abstract/Free Full Text]

97. Yanaihara N., Caplen N., Bowman E., Seike M., Kumamoto K., Yi M., Stephens R.M., Okamoto A., Yokota J., Tanaka T., et al. Unique microRNA molecular profiles in lung cancer diagnosis and prognosis. Cancer Cell (2006) 9:189–198.[CrossRef][Web of Science][Medline]

98. Murakami Y., Yasuda T., Saigo K., Urashima T., Toyoda H., Okanoue T., Shimotohno K. Comprehensive analysis of microRNA expression patterns in hepatocellular carcinoma and non-tumorous tissues. Oncogene (2006) 25:2537–2545.[CrossRef][Web of Science][Medline]

99. Roldo C., Missiaglia E., Hagan J.P., Falconi M., Capelli P., Bersani S., Calin G.A., Volinia S., Liu C.G., Scarpa A., et al. MicroRNA expression abnormalities in pancreatic endocrine and acinar tumors are associated with distinctive pathologic features and clinical behavior. J. Clin. Oncol. (2006) 24:4677–4684.[Abstract/Free Full Text]

100. Lee E.J., Gusev Y., Jiang J., Nuovo G.J., Lerner M.R., Frankel W.L., Morgan D.L., Postier R.G., Brackett D.J., Schmittgen T.D. Expression profiling identifies microRNA signature in pancreatic cancer. Int. J. Cancer (2007) 120:1046–1054.[CrossRef][Web of Science][Medline]

101. Szafranska A.E., Davison T.S., John J., Cannon T., Sipos B., Maghnouj A., Labourier E., Hahn S.A. MicroRNA expression alterations are linked to tumorigenesis and non-neoplastic processes in pancreatic ductal adenocarcinoma. In: Oncogene (2007) Epub ahead of print 22 Jan 2007, doi: 10.1038/sj.onc.1210228.

102. Eis P.S., Tam W., Sun L., Chadburn A., Li Z., Gomez M.F., Lund E., Dahlberg J.E. Accumulation of miR-155 and BIC RNA in human B cell lymphomas. Proc. Natl Acad. Sci. USA (2005) 102:3627–3632.[Abstract/Free Full Text]

103. Ciafre S.A., Galardi S., Mangiola A., Ferracin M., Liu C.G., Sabatino G., Negrini M., Maira G., Croce C.M., Farace M.G. Extensive modulation of a set of microRNAs in primary glioblastoma. Biochem. Biophys. Res. Commun. (2005) 334:1351–1358.[CrossRef][Web of Science][Medline]

104. Chen Y., Stallings R.L. Differential patterns of microRNA expression in neuroblastoma are correlated with prognosis, differentiation, and apoptosis. Cancer Res. (2007) 67:976–983.[Abstract/Free Full Text]

105. Martin M.M., Lee E.J., Buckenberger J.A., Schmittgen T.D., Elton T.S. MicroRNA-155 regulates human angiotensin II type 1 receptor expression in fibroblasts. J. Biol. Chem. (2006) 281:18277–18284.[Abstract/Free Full Text]

106. Kawasaki H., Taira K. MicroRNA-196 inhibits HOXB8 expression in myeloid differentiation of HL60 cells. In: Nucleic Acids Symp. Ser (Oxf.) (2004) 211–212.

107. Garzon R., Pichiorri F., Palumbo T., Visentini M., Aqeilan R., Cimmino A., Wang H., Sun H., Volinia S., Alder H., et al. MicroRNA gene expression during retinoic acid-induced differentiation of human acute promyelocytic leukemia. In: Oncogene (2007) Epub ahead of print 29 Jan 2007, doi: 10.1038/sj.onc.1210186.

108. Fazi F., Rosa A., Fatica A., Gelmetti V., De Marchis M.L., Nervi C., Bozzoni I. A minicircuitry comprised of microRNA-223 and transcription factors NFI-A and C/EBPalpha regulates human granulopoiesis. Cell (2005) 123:819–831.[CrossRef][Web of Science][Medline]

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