期刊文献+

miR-181c-3p和miR-5692b在食管癌患者中的表达水平及其临床意义 被引量:6

Expression levels of miR-181c-3p and miR-5692b in esophageal cancer and their clinical significance
原文传递
导出
摘要 目的探讨miR-181c-3p和miR.5692b在食管癌患者中的表达水平及临床意义。方法应用基因芯片技术对食管癌组织的特异性microRNA进行筛查,然后利用即时荧光定量PCR技术对55例食管癌及癌旁对照组织的miR-181c.3p和miR-5692b表达情况进行检测。结果(1)癌组织中miR-181c.3p与miR-5692b的表达水平均较正常组织升高。(2)miR181c-3p和miR-5692b表达水平均与肿瘤大小、浸润深度及临床分期相关(均P〈0.05)。(3)miR-181c-3p和miR-5692b高表达组总生存率明显低于低表达组(均P〈0.05)。(4)多元Cox回归分析结果表明高表达miR-181c-3p和miR-5692b均为食管癌的预后不良因素。结论miR-181c-3p和miR-5692b的表达与食管癌的临床病理特征及预后存在显著相关性,可作为食管癌进展和预后的潜在预测指标。 Objective To study the expression level and clinical significance of miR-181c-3p and miR-5692b in esophageal cancer. Methods The microRNA (miRNA) profiles of esophageal squamous cell carcinoma were analyzed by miRNA microarray in 55 cases of esophageal cancer. The expression levels of miR-181c-3p and miR-5692b from 55 pairs of tumor tissues and adjacent non-neoplastic tissues were determined by qRT-PCR analysis. Results Both miR-181c-3p and miR-5692b were significantly up- regulated in tumor tissues compared with adjacent non-neoplastic tissues. Their expression was also significantly associated with tumor size, depth of invasion and clinical tumor stage ( P 〈 0. 05 ) . High expression of miR-181c-3p and miR-5692b were significantly associated with poor prognosis (P 〈 0. 05 ). Multivariate Cox regression analysis confirmed that high expression of miR-181c-3p and miR-5692b was poor prognostic indicators in esophageal cancer. Conclusions There are significant correlation between miR-181c-3p/miR-5692b expression, clinicopathologic parameters and prognosis. They represent potential prognostic biomarkers in esophageal squamous cell carcinoma.
出处 《中华病理学杂志》 CAS CSCD 北大核心 2015年第12期905-909,共5页 Chinese Journal of Pathology
基金 新疆重大疾病医学重点实验室开放课题(SKLIB-XJMDR-2012-7)
关键词 食管肿瘤 微RNAS 预后 病理学 外科 Esophageal neoplasms MicroRNAs Prognosis Pathology, surgical
  • 相关文献

参考文献4

二级参考文献89

  • 1Lee RC, Feinhaum RL, Amhros V. The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14. Cell, 1993, 75(5) :843-854.
  • 2Friedman RC, Farh KK, Burge CB, et al. Most mammalian mR.NAs are conserved targets of microRNAs. Genome Res, 2009, 19( 1 ) :92-105.
  • 3Calin GA, Dumitru CD, Shimizu M, et al. Frequent deletions and down-regulation of micro- RNA genes miR15 and miR16 at 13q14 in chronic lymphocytic leukemia. Proc Natl Acad Sci U S A, 2002,99 ( 24 ) : 15524-15529.
  • 4Lu J, Getz G, Miska EA, et al. MicroRNA expression profiles classify human cancers. Nature, 2005, 435 (7043) :834-838.
  • 5] O'Donnell KA, Wentzel EA, Zeller KI, et al, c-Myc-regulated microRNAs modulate E2F1 expression. Nature, 2005, 435 ( 7043 ) : 839-843.
  • 6He L, Thomson JM, Hemann MT, et al. A mieroRNA polycistron as a potential human oncogene. Nature, Nature. 2005 Jun 9;435 ( 7043 ) : 828-833.
  • 7Mavrakis K J, Wolfe AL, Oricchio E, et al. Genome-wide RNA- mediated interference screen identifies miR-19 targets in Notch- induced T-cell acute lymphoblastic leukaemia. Nat Cell Biol, 2010,12 (4) :372-379.
  • 8Taguchi A, Yanagisawa K, Tanaka M, et al. Identification of hypoxia-inducible factor-1 alpha as a novel target for miR-17-92 microRNA cluster. Cancer Res, 2008, 68(14) :5540-5545.
  • 9Li H, Bian C, Liao L, et al. miR-17-5p promotes human breast cancer cell migration and invasion through suppression of HBP1. Breast Cancer Res Treat, 2011,126 (3) :565-575.
  • 10Guttilla IK, White BA. Coordinate regulation of FOXO1 by miR-27a, miR-96, and miR-182 in breast cancer cells. J Biol Chem, 2009,284 ( 35 ) :23204-23216.

共引文献11

同被引文献50

引证文献6

二级引证文献6

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