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肝细胞癌中microRNA对细胞凋亡、转移和周期的调控作用 被引量:11

Regulatory effect of miRNAs on apoptosis,migration,and cell cycle of hepatocellular carcinoma cells
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摘要 microRNA(miRNA)是一类由内源基因编码的长度约为22个核苷酸的非编码单链RNA分子,参与转录后基因表达调控。大量证据显示一些miRNA在肝细胞癌(HCC)中表达失调,且发现miRNA通过一些通路或基因调控癌细胞的增殖、凋亡、转移、侵袭和细胞周期。另外,也有一些研究认为miRNA是癌基因或抑癌基因。因此,深入的了解miRNA在HCC中的具体作用和功能,或许会为HCC的治疗提供新的途径。 MicroRNAs (miRNAs) are a class of non - coding single - stranded RNA molecules of about 22 nucleotides in length that are en- coded by endogenous gene and participate in post - transcriptional regulation of gene expression. Many evidences indicate that some miRNAs are deregulated in hepatocellular carcinoma (HCC) , and it has been found that miRNAs regulate the proliferation, apoptosis, migration, in- vasion, and cell cycle of HCC cells through some pathways or genes. In addition, some studies suggest that miRNAs function as oncogenes or anti - oncogenes. Therefore, in - depth understanding of the specific role and function of miRNAs in HCC may provide a new approach for the treatment of HCC.
出处 《临床肝胆病杂志》 CAS 2013年第7期554-557,共4页 Journal of Clinical Hepatology
关键词 肝肿瘤 微RNAS 细胞凋亡 肿瘤转移 肿瘤侵润 细胞周期 liver neoplasms microRNAs apoptosis neoplasm metastasis neoplasm invasiveness cell cycle
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  • 1Abou E1 Hassan, M.A., Mastenbroek, D.C., Gerritsen, W.R., Giaccone, G., Kruyt, EA., 2004. Overexpression of Bcl2 abrogates chemo- and radiotherapy-induced sensitisation of NCI-H460 non-small-cell lung cancer cells to adenovirus-mediated expression of full-length TRAIL. Br. J. Cancer 91. 171--177.
  • 2Aravalli, R.N., Steer, C.J., Cressman, E.N., 2008. Molecular mechanisms of hepatocellular carcinoma. Hepatology 48, 2047--2063.
  • 3Barrel, D.E, 2004. MicroRNAs: genomics, biogenesis, mechanism, and function. Cell 116, 281--297.
  • 4Calin, G.A., Sevignani, C., Dumitru, C.D., Hyslop, T., Noch, E., Yendamuri, S., Shimizu, M., Rattan, S., Bullrich, F., Negrini, M., Croce, C.M., 2004. Human microRNA genes are frequently located at fragile sites and genomic regions involved in cancers. Proc. Natl. Acad. Sci. USA 101, 2999--3004.
  • 5Cimmino, A., Calin, G.A., Fabbri, M., Iorio, M.V., Ferracin, M., Shimizu, M., Wojcik, S.E., Aqeilan, R.I., Zupo, S., Dono, M., Rassenti, L., Alder, H., Volinia, S., Liu, C.G., Kipps, T.J., Negrini, M., Croce, C.M., 2005. miR-15 and miR-16 induce apoptosis by targeting BCL2. Proc. Natl. Acad. Sci. USA 102. 13944-13949.
  • 6Danial, N.N., 2007. BCL-2 family proteins: critical checkpoints of apoptotic cell death. Clin. Cancer Res. 13, 7254--7263.
  • 7Degterev, A., Boyce, M., Yuan, J., 2003. A decade of caspases. Oncogene 22, 8543--8567.
  • 8Hanahan, D., Weinberg, R.A., 2000. The hallmarks of cancer. Cell 100, 57--70.
  • 9Ichimi, T., Enokida, H., Okuno, Y., Kunimoto, R., Chiyomaru, T., Kawamoto, K., Kawahara, K., Toki, K., Kawakami, K., Nishiyama, K., Tsujimoto, G., Nakagawa, M., Seki, N., 2009. Identification of novel microRNA targets based on microRNA signatures in bladder cancer. Int. J. Cancer 125. 345--352.
  • 10Iorio, M.V., Ferracin, M., Liu, C.G., Veronese, A., Spizzo, R., Sabbioni, S., Magri, E., Pedriali, M., Fabbri, M., Campiglio, M., Menard, S., Palazzo, J.E, Rosenberg, A., Musiani, E, Volinia, S., Nenci, I., Calin, G.A., Querzoli, E, Negrini, M., Croce, C.M., 2005. MicroRNA gene expression deregulation in human breast cancer. Cancer Res. 65, 7065--7070.

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