期刊文献+

胃癌组织中miR-181a及其靶基因KLF6表达变化及意义 被引量:1

EXPRESSION AND SIGNIFICANCE OF MIR- 181A AND KLF6 IN GASTRIC CARCINOMA TISSUES
下载PDF
导出
摘要 目的观察胃癌组织中微小RNA(miRNA)-181a(miR-181a)与其靶基因Kruppel样因子6(Kruppel like factor 6,KLF6,又称锌指转录因子9或核心启动子元件结合蛋白)的表达变化,并探讨其意义。方法 9例胃癌患者,手术时留取癌组织及癌旁组织,抽提其中的总RNA及蛋白质,采用实时荧光定量PCR检测标本中的miR-181a,Western blot检测KLF6蛋白。结果胃癌组织中miR-181a的表达量(2-△△Ct)为(1.981±1.080),癌旁组织miR-181a的表达量为(0.394±0.093);癌组织KLF6蛋白灰度值为(0.241 6±0.135 5),癌旁组织为(0.540 2±0.05 5),两种组织中的miR-181a、KLF6蛋白表达量相比,均p﹤0.01;miR-181a与KLF6蛋白的表达呈负相关(r=-0.590,p﹤0.01)。结论胃癌组织中miR-181a表达明显上调,KLF6蛋白表达明显下降;结合前期实验研究,我们推测miR-181a可能通过转录后基因沉默机制使KLF6蛋白表达下降,从而促进胃癌的发生发展。 Objective To investigate the expression and significance of microRNA( miRNA)-181a( miR-181a) and its target gene Kruppel like factor 6( KLF6) in gastric carcinoma tissues. Methods The gastric carcinoma and adjacent non- tumorous tissues were collected( from 9 patients) respectively and the total RNA and protein were extracted routinely. The miR- 181a was detected by Real- time quantitative PCR. KLF6 protein were detected by Western blot. Results In gastric carcinoma tissues,the miR- 181a and KLF6 protein was( 1. 981 ± 1. 080),( 0.241 6 ±0.135 5),respectively,whereas in the adjacent non-tumorous tissues,the miR-181a and KLF6 protein was( 0. 394 ± 0. 093),( 0. 540 2 ± 0. 055),respectively. The differeace between the expression of miR- 181a and KLF6 protein in these two tissues was statistically significant( all p ﹤ 0. 01). There was a remarkable inverse correlation between miR- 181a and KLF6 protein levels was observed( r =- 0. 590,p ﹤ 0. 01). Conclusion The expression of miR- 181a was significantly up- regulated in gastric carcinoma tissues,whereas the KLF6 protein was markedly decreased. Based on the previous research,we speculate that miR- 181a may inhibit KLF6 expression by post- transcriptional gene silencing to restrain gastric carcinoma occurrence and progress.
出处 《现代医院》 2014年第5期9-12,共4页 Modern Hospitals
基金 广东省自然科学基金(编号:NO.10151006001000016)
关键词 胃癌 微小RNA KLF6基因 miR-181a Gastric cancer micro-RNA KLF6 miR-181a
  • 相关文献

参考文献24

  • 1CIAFRE SA, GALARDI S, MANGIOLA A, et al. Extensive modu- lation of a set of microRNAs in primary glioblastoma[ J ]. Biochem Biophys Res Commun, 2005,334 ( 4 ) : 1351 - 1358.
  • 2JI J, YAMASHITA T, BUDHU A, et al. Identification of microRNA - 181 by genome -wide screening as a critical player inEpCAM - positive hepatic cancer stem cells [ J ]. Hepatology, 2009,50 ( 2 ) : 472 - 480.
  • 3ANDREOLI V, GEHRAU R C,BOCCO J L. Biology of Kruppel - like factor 6 transcriptional regulator in cell life anddeath[ J]. IUB- MB Life,2010,62(12) :896 -905.
  • 4RATZIU V, LALAZAR A, WONG L, et al. Zig, a Kruppel - like transcription factor up - regulated in vivo during earlyhepatic fibro- sis[J]. Proc Natl Acad Sci U S A,1998,95(16) :9500 -9505.
  • 5SANGODKAR J, SHI J, DIFEO A, et al. Functional role of the KLF6 tumour suppressor gene in gastric cancer[ J]. Eur J Cancer, 2009,45 (4) :666 -676.
  • 6CHO Y G,KIM C J,PARK C H,et al. Genetic alterations of the KLF6 gene in gastric cancer [ J ]. Oncogene, 2005,24 ( 28 ) : 4588 - 4590.
  • 7刘权溢,阮荻行,林灼怡.腹腔镜与开腹胃癌切除手术的对比研究[J].现代医院,2011,11(7):30-32. 被引量:20
  • 8刘少列,郑卫军.肿瘤标志物CEA、CA199对胃癌的诊断价值[J].现代医院,2011,11(11):59-60. 被引量:3
  • 9VOLINIA S,CALIN G A,LIU C G,et aL A microRNA expression signature of human solid tumors defines cancer genetargets [ J ]. Proc Nail Acad Sci U S A,2006,103(7) :2257 -2261.
  • 10LU J, GETZ G, MISKA E A, et al. MicmRNA expression profiles classify human cancers [ J ]. Nature,2005,435 ( 7043 ) : 834 - 838.

二级参考文献11

共引文献21

同被引文献25

  • 1STEEGERS E A, VON DADELSZEN P, DUVEKOT J J, et al. Pre - eclampsia [ J ]. The Lancet,2010,376 ( 9741 ) : 631 - 644.
  • 2NALJAYAN M V, S ANANTH K. New developments in the path- ogenesis of preeclampsia [ J ]. Advances in Chronic Kidney Dis- ease, 2013, 20(20) : 265 -270.
  • 3BARTEL D P. MicroRNAs: Genomics, Biogenesis, Mechanism, and Function[J]. Cell, 2004, 116(2) : 281 -297.
  • 4ENGELS B M, HUTVAGNER G. Principles and effects of mi- croRNA - mediated post - transcriptional gene regulation[ J]. On-cogene, 2006, 25(46): 6163-6169.
  • 5IVEY K N, SRIVASTAVA D. MicroRNAs as regulators of differ- entiation and cell fate decisions [ J]. Cell Stem Cell, 2010, 7 (1): 36 -41.
  • 6HIME G R, W GREGORY S. Micro - RNA mediated regulation of proliferation, self - renewal and differentiation of mammalian stem cells[J]. Cell Adhesion & Migration, 2009, 3(4) : 425 -432.
  • 7CHENG A M, BYROM M W, JEFFREY S, et al. Antisense inhi- bition of human miRNAs and indications for an involvement of miRNA in cell growth and apoptosis [ J ]. Nucleic Acids Research, 2005, 33(4) : 1290 - 1297.
  • 8XIAO - MING Z, TAO H, SARGENT I L, et al. Differential ex- pression profile of microRNAs in human placentas from preeclamp- tic pregnancies vs normal pregnancies [ J ]. American Journal of Obstetrics & Gynecology, 2009, 200(6) : 661.
  • 9ENQUOBAHRIE D A, ABETEW D F, SORENSEN T K, et al. Placental microRNA expression in pregnancies complicated by pre- eclampsia [ J ]. American Journal of Obstetrics & Gynecology, 2011,204(2) : 112 - 178.
  • 10WANG W, FENG L, ZHANG H, et al. Preeclampsia up - regu- lates angiogenesis - associated microRNA ( i. e. , miR - 17, - 20a, and -20b) that target ephrin- B2 and EPHB4 in human placenta [ J ]. Joumal of Clinical Endocrinology & Metabolism, 2012, 97(6) : 1051 -1059.

引证文献1

二级引证文献4

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