MiRNAs as promising biomarkers in cancer

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Abstract

By 2004 according to the resuts of the international genome sequencing, about 20,000 protein-coding genes had been analyzed which correspond to more than 2% of the total genomic sequence. The vast majority of gene transcripts are actually characterized as non-coding RNA (ncRNA) and are a cluster of RNA that do not encode functional proteins. They can be small, approximately 20 nucleotides in length, known as microRNAs (miRNAs), or transcripts longer than 200 nucleotides, defined as long non-coding RNAs (lncRNAs). miRNAs are short ncRNAs that are involved in the post-transcriptional regulation of gene expression. Discovered over 15 years ago, these molecules have been recognized as one of the main regulatory molecules in the human genome. They play an important role in all biological processes being important modulators of the eukaryotic genes expression. Focusing on transcripts that encode proteins, miRNAs influence the cellular transcript, thereby helping to determine the outcome of the cell. Aberrant miRNA expression was observed in cancer patients. Tissue concentrations of specific miRNAs have been shown to be associated with tumor invasiveness, metastatic potential, and other clinical characteristics for many types of cancer. Compared to traditional biomarkers like proteins, miRNA has several advantages that will allow them to be considered as new potential biomarkers in cancer. This review looks at biogenesis, functions, technologies used to detect miRNA, and the association of miRNA with human cancer, in particular, colorectal cancer.

About the authors

Andrian A. Tarmaev

Harbin Medical University

Email: Tarmaevandrian@outlook.com
China, Harbin

Ozal A. Beylerli

Bashkir State Medical University

Author for correspondence.
Email: obeylerli@mail.ru
ORCID iD: 0000-0002-6149-5460
Russian Federation, Ufa

References

  1. Kulasingam V, Diamandis EP. Strategies for discovering novel cancer biomarkers through utilization of emerging technologies. Nat Clin Pract Oncol. 2008;5(10):588-599. https://doi.org/10.1038/ncponc1187.
  2. Lei EP, Silver PA. Protein and RNA export from the nucleus. Dev Cell. 2002;2(3):261-272. https://doi.org/10.1016/s1534-5807(02)00134-x.
  3. Behm-Ansmant I, Rehwinke J, Doerks T, et al. MRNA degradation by miRNAs and GW182 requires both CCR4: NOT deadenylase and DCP1:DCP2 decapping complexes. Genes Dev. 2006;20(14):1885-1898. https://doi.org/10.1101/gad.1424106.
  4. Nishihara T, Zekri L, Braun JE, Izaurralde E. miRISC recruits decapping factors to miRNA targets to enhance their degradation. Nucleic Acids Res. 2013;41(18):8692-8705. https://doi.org/10.1093/nar/gkt619.
  5. Vasudevan S, Tong Y, Steitz JA. Switching from repression to activation: microRNAs can up-regulate translation. Science. 2007;318(5858):1931-1934. https://doi.org/10.1126/science.1149460.
  6. Wilson RC, Doudna JA. Molecular mechanisms of RNA interference. Annu Rev Biophys. 2013;42:217-239. https://doi.org/10.1146/annurev-biophys-083012-130404.
  7. Friedman RC, Farh KK, Burge CB, Bartel DP. Most mammalian mRNAs are conserved targets of microRNAs. Genome Res. 2009;19(1):92-105. https://doi.org/10.1101/gr.082701.108.
  8. Gregory RI, Yan KP, Amuthan G, et al. The microprocessor complex mediates the genesis of microRNAs. Nature. 2004;432(7014):235-240. https://doi.org/10.1038/nature03120.
  9. Lund E, Guttinger S, Calado A, et al. Nuclear export of microRNA precursors. Science. 2004;303(5654):95-98. https://doi.org/10.1126/science.1090599.
  10. Lee Y, Ahn C, Han J, et al. The nuclear RNase III Drosha initiates microRNA processing. Nature. 2003;425(6956):415-419. https://doi.org/10.1038/nature01957.
  11. Lee Y, Jeon K, Lee JT, et al. MicroRNA maturation: stepwise processing and subcellular localization. EMBO J. 2002;21(17):4663-7460. https://doi.org/10.1093/emboj/cdf476.
  12. Link A, Balaguer F, Shen Y, et al. Fecal micro-RNA as novel biomarkers for colon cancer screening. Cancer Epidemiol Biomarkers Prev. 2010;19(7):1766-1774. https://doi.org/10.1158/1055-9965.EPI-10-0027.
  13. Kalimutho M, Di Cecilia S, Del Vecchio Blanco G, et al. Epigenetically silenced miR-34bc as a novel faecal-based screening marker for colorectal cancer. Br J Cancer. 2011;104(11):1770-1778. https://doi.org/10.1038/bjc.2011.82.
  14. Dong Y, Wu WK, Wu CW, et al. MicroRNA dysregulation in colorectal cancer: a clinical perspective. Br J Cancer. 2011;104(6):893-898. https://doi.org/10.1038/bjc.2011.57.
  15. Koga Y, Yasunaga M, Takahashi A, et al. MicroRNA expression profiling of exfoliated colonocytes isolated from feces for colorectal cancer screening. Cancer Prev Res (Phila). 2010;3(11):1435-1442. https://doi.org/10.1158/1940-6207.CAPR-10-0036.
  16. Wang X, Kuang YY, Hu XT. Advances in epigenetic biomarker research in colorectal cancer. World J Gastroenterol. 2014;20(15):4276-4287. https://doi.org/10.3748/wjg.v20.i15.4276.
  17. Mazeh H, Mizrahi I, Ilyayev N, et al. The diagnostic and prognostic role of microRNA in colorectal cancer: a comprehensive review. J Cancer. 2013;4(3):281-295. https://doi.org/10.7150/jca.5836.
  18. Nugent M, Miller N, Kerin MJ. MicroRNAs in colorectal cancer: function, dysregulation and potential as novel biomarkers. Eur J Surg Oncol. 2011;37(8):649-654. https://doi.org/10.1016/j.ejso.2011.05.005.
  19. Ferracin M, Veronese A, Negrini M. Micromarkers: miRNAs in cancer diagnosis and prognosis. Expert Rev Mol Diagn. 2010;10(3):297-308. https://doi.org/10.1586/erm.10.11.
  20. Menendez P, Villarejo P, Padilla D, et al. Implications of the histological determination of microRNA in the screening, diagnosis and prognosis of colorectal cancer. J Surg Oncol. 2013;108(1):70-73. https://doi.org/10.1002/jso.23344.
  21. Menendez P, Padilla D, Villarejo P, et al. Prognostic implications of serum microRNA-21 in colorectal cancer. J Surg Oncol. 2013;108(6):369-373. https://doi.org/10.1002/jso.23415.
  22. Chen X, Ba Y, Ma L, et al. Characterization of micro-RNA in serum: a novel class of biomarkers for diagnosis of cancer and other diseases. Cell Res. 2008;18(10):997-1006. https://doi.org/10.1038/cr.2008.282.
  23. Ng EK, Chong WW, Jin H, et al. Differential expression of micro-RNA in plasma of patients with colorectal cancer a potential marker for colorectal cancer screening. Gut. 2009;58(10):1375-1381. https://doi.org/10.1136/gut.2008.167817.
  24. Huang Z, Huang D, Ni S, et al. Plasma micro-RNA are promising novel biomarkers for early detection of colorectal cancer. Int J Cancer. 2010;127(1):118-126. https://doi.org/10.1002/ijc.25007.
  25. Pu XX, Huang GL, Guo HQ, et al. Circulating miR-221 directly amplified from plasma is a potential diagnostic and prognostic marker of colorectal cancer and is correlated with p53 expression. J Gastroenterol Hepatol. 2010;25(10):1674-1680. https://doi.org/10.1111/j.1440-1746.2010.06417.x.
  26. Kanaan Z, Roberts H, Eichenberger MR, et al. A plasma microRNA panel for detection of colorectal adenomas: a step toward more precise screening for colorectal cancer. Ann Surg. 2013;258(3):400-408. https://doi.org/10.1097/SLA.0b013e3182a15bcc.
  27. Cheng H, Zhang L, Cogdell DE, et al. Circulating plasma MiR-141 is a novel biomarker for metastatic colon cancer and predicts poor prognosis. PLoS One. 2011;6(3):e17745. https://doi.org/10.1371/journal.pone. 0017745.
  28. Wang LG, Gu J. Serum microRNA-29a is a promising novel marker for early detection of colorectal liver metastasis. Cancer Epidemiol. 2012;36(1):e61-67. https://doi.org/10.1016/j.canep.2011.05.002.
  29. Menendez P, Villarejo P, Padilla D, et al. Diagnostic and prognostic significance of serum micro-RNA in colorectal cancer. J Surg Oncol. 2013;107(2):217-220. https://doi.org/10.1002/jso.23245.

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Copyright (c) 2019 Tarmaev A.A., Beylerli O.A.

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