期刊文献+

MiR-497的研究进展 被引量:3

Advances of researches on MiR-497
下载PDF
导出
摘要 本文概述了miR-497的生物学功能以及它在多种肿瘤、缺血性疾病等中的作用。miR-497在细胞分裂、代谢、应激以及大脑不同区域具有非常重要的生物学功能。多项研究证明miR-497在乳腺癌、结肠直肠癌、原发性腹膜癌、肾上腺素皮质癌(ACC)、黑色素瘤、脑颈部鳞状细胞癌等多种肿瘤中低表达,体内外过表达miR-497可以引起肿瘤细胞凋亡,证明miR-497在抗肿瘤方面发挥着重要作用;另外,miR-497在缺血性脑卒中也具有重要作用。因而,miR-497具有良好的临床分子靶向治疗应用前景。 This article summarizes the biological functions of miR-497 and its role in a variety of tumors and ischemic diseases. MiR-497 plays important biological roles in cell division, metabolism, stress and different brain regions. A number of studies have proved that miR-497 displays low expression in breast cancer, colorectal cancer, primary peritoneal carcinoma, epinephrine cortical carcinoma (ACC), melanoma, brain cervical squamous cell carcinoma, and so on. Overexpression of miR-497 can cause tumor cell apoptosis in vitro, which verifies miR-497 roles in antitumor and ischemic stroke. Therefore, miR-497 has a great potential for clinical targeted molecular therapy.
出处 《国外医学(医学地理分册)》 CAS 2013年第2期125-128,共4页 Foreign Medical Sciences:Section of Medgeography
基金 国家自然科学基金(No.30400249) 陕西省自然科学基金(No.2010K16-04) 2009年西安交通大学校基金(No.xjj2009079) 2010年中央高校基本科研业务费专项基金项目(No.xjj20100031) 2012年西安交通大学本科生科研训练和实践创新基金项目(No.22012185 No.2013273)
关键词 miR-497 细胞分裂 细胞代谢 应激 肿瘤发生 miR-497 cell division cell metabolism stress oncogenesis
  • 相关文献

参考文献26

  • 1Li D, Zhao Y, Liu C, et al. Analysis of MiR-195 and MiR-497 expression, regulation and role in breast cancer [J]. Clin Canc- er Res,2011,17 (7):1722-1730.
  • 2Finnerty JR, Wang WX, Hebert SS, et al. The miR-15/107 group of microRNA genes: evolutionary biology, cellular func- tions, and roles in human diseases [J]. J Mol Biol, 2010, 402 (3) ,491-509.
  • 3Guo ST, Jiang CC, Wang GP, et al. MicroRNA-497 targets in- sulin-like growth factor 1 receptor and has a tumour suppres- sive role in human colorectal cancer[J]. Oncogene. 2013, 32 (15) :1910-1920.
  • 4Flavin RJ, Smyth PC, Laios A, et al. Potentially important mi- croRNA cluster on chromosome 17p13.1 in primary peritoneal carcinoma [J]. Mod Pathol, 2009,22 (2) : 197-205.
  • 5Liu Q, Fu H, Sun F, et al. miR-16 family induces cell cycle ar- rest by regulating multiple cell cycle genes [J]. Nucleic Acids Res,2008,36(16) :5391-5404.
  • 6Bandi N, Zbinden S, Gugger M, et al. miR-15a and miR-16 are implicated in cell cycle regulation in a Rb-dependent manner and are frequently deleted or down-regulated in non-small cell lung cancer [J]. Cancer Res,2009,69(13):5553-5559.
  • 7Wang F, Fu XD, Zhou Y, et al. Down-regulation of the cyclin E1 oncogene expression by microRNA-16-1 induces cell cycle arrest in human cancer cells [J]. BMB Rep, 2009,42(11): 725-730.
  • 8Shen L, Li J, Xu L, et al. miR-497 induces apoptosis of breast cancer cells by targeting Bcl-w [J]. Exp Ther Med,2012,3(3) : 475-480.
  • 9Tang X, Muniappan L, Tang G, et al. Identification of glu- cose-regulated miRNAs from pancreatic {beta} cells reveals a role for miR-30d in insulin transcription [J]. Rna, 2009,15 (2) : 287-293.
  • 10Marsit CJ, Eddy K, Kelsey KT. MicroRNA responses to cellu- lar stress[J]. Cancer Res,2006,66 (22) :10843-10848.

同被引文献38

  • 1Li D, Zhao Y, Liu C, et al. Analysis of mir-195 and miR-497 expression, regulation and role in breast cancer [J]. Clin Cancer Res,2011,17(7) :1722-1730.
  • 2Creevey L, Ryan J, Harvey H, et al. Microrna-497 increases apoptosis in mycn amplified neuroblastoma cells by targeting the key cell cycle regulator wee1 [J]. Mol Cancer, 2013,12:23- 25.
  • 3Lew DJ, Dulic V, Reed SI. Isolation of three novel human cyclins by rescue of gl cyclin (cln) function in yeast [J]. Cell, 1991,66(6) :1197-1206.
  • 4Luo Q, Li X, Gao Y, et al. Mirna-497 regulates cell growth and invasion by targeting cyclin el in breast cancer [J]. Cancer Cell Int, 2013,13(1) :95-98.
  • 5FurutaM, Kozaki K, Tanimoto K, et al. The tumor- suppressive miR.497-195 cluster targets multiple cell-cycle regulators in hepatocellular carcinoma [J]. PLoS One, 2013,8 (3) :e60155-e60157.
  • 6Rameh LE, Cantley LC. The role of phosphoinositide 3-kinase lipid products in cell function [J]. J Biol Chem, 1999,274 (13) : 8347-8350.
  • 7Downward J. Mechanismsand consequences of activation of protein kinase b/akt [J]. Curr Opin Cell Biol, 1998,10(2) : 262- 267.
  • 8Shaw RJ, Cantley LC. Ras, pi (3)k and rotor signalling controls tumour cell growth [J]. Nature, 2006,441 (7092) : 424- 430.
  • 9Raught B, Gingras AC,Sonenberg N. The target of rapamycin (tor) proteins [J]. Proc Natl Acad Sci U S A, 2001,98 (13): 7037-7044.
  • 10Guo ST, Jiang CC, Wang GP, et al. Microrna-497 targets insulin-like growth factor 1 receptor and has a tumour suppressive role in human colorectal cancer [J]. Oneogene, 2013,32(15) :1910-1920.

引证文献3

二级引证文献17

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部