期刊文献+

结直肠癌及癌旁组织中miR-338-3p及MACC1的表达变化及意义 被引量:5

Expressions and significance of mi R-338-3p and MACC1 in colorectal carcinoma and adjacent non-tumorous tissues
下载PDF
导出
摘要 目的观察结直肠癌组织中mi R-338-3p与结直肠癌转移相关基因1(metastasis-associated in colon cancer-1,MACC1)的表达变化,并探讨其意义。方法收集昆明医科大学第二附属医院2015年1月-2015年5月外科手术切除并经病理证实的15例结直肠癌患者,手术时留取癌组织及癌旁组织,采用实时荧光定量PCR检测mi R-338-3p的表达,免疫组化检测MACC1的表达,双荧光素酶报告检测mi R-338-3p与MACC1。结果结直肠癌组织及癌旁组织中mi R-338-3p的相对表达量分别为0.022±0.005和0.071±0.002,差异有统计学意义(P<0.05);MACC1在结直肠癌组织中的阳性表达率(66.7%)显著高于癌旁组织(20.0%),差异有统计学意义(P<0.01);mi R-338-3p与MACC1的表达呈负相关(r=-0.798,P<0.01),mi R-338-3p抑制MACC1的表达。结论mi R-338-3p可能通过转录后基因沉默机制抑制MACCI的表达,从而抑制结直肠癌的发生。 Objective To observe the expressions of mi R-338-3p and MACC1 in colorectal carcinoma tissues and to investigate the significance. Methods The colorectal carcinoma tissues and adjacent non-tumorous tissues were collected(15 patients) respectively in the Second Affiliated Hospital of Kunming Medical University from Jan. 2015 to May.2015,which were confirmed by pathology. Mi R-338-3p was detected by Real-time quantitative PCR. MACC1 was detected by immunohistochemical technique. The correlation between mi R-338-3p and MACC1 was detected by pual luciferase report system. Results The expressions of mi R-338-3p in colorectal carcinoma tissues and adjacent non-tumorous tissues were 0. 022 ± 0. 005 and 0. 071 ± 0. 002,respectively,the difference was significant( P〈0. 05); the positive rate of MACC1 in colorectal carcinoma(66. 7%) was higher than that in adjacent non-tumorous tissues(20. 0%)( P〈0. 01); there was negative correlation between mi R-338-3p and MACC1( r =- 0. 798,P〈0. 01). Mi R-338-3p inhibited the expression of MACC1. Conclusion Mi R-338-3p may inhibit the MACC1 expression by post-transcriptional gene silencing to interdict the occurrence and progress of colorectal carcinoma.
出处 《胃肠病学和肝病学杂志》 CAS 2017年第2期139-141,共3页 Chinese Journal of Gastroenterology and Hepatology
基金 云南省应用基础研究计划项目(2013FB155)
关键词 结直肠癌 微小RNA 结直肠癌转移相关基因 Colorectal carcinoma Micro-RNA Metastasis-associated in colone cancer-1
  • 相关文献

参考文献2

二级参考文献14

  • 1Kai SUN Qian WANG Xiao-hui HUANG.PPAR gamma inhibits growth of rat hepatic stellate cells and TGF beta-induced connective tissue growth factor expression[J].Acta Pharmacologica Sinica,2006,27(6):715-723. 被引量:35
  • 2Calin GA,Croce CM.MicroRNA-cancer connection:the beginning of a new tale.Cancer Res,2006,66(15):7390-7394.
  • 3Calin GA,Liu CG,Sevignani C,et al.MicroRNA profiling reveals distinct signatures in B cell chronic lymphocytic leukemias.Proc Natl Acad Sci USA,2004,101(32):11755-11760.
  • 4Peck D,Crawford ED,Ross KN,et al.A method for high-throughput gene expression signature analysis.Genome Biol,2006,7(7):R61.
  • 5Murakami Y,Yasuda T,Saigo K,et al.Comprehensive analysis of microRNA expression patterns in hepatocellular carcinoma and nontumorous tissues.Oncogene,2006,25(17):2537-2545.
  • 6Gramantieri L,Ferracin M,Fornari F,et al.Cyclin G1 is a target of miR-122a,a microRNA frequently down-regulated in human hepatocellular carcinoma.Cancer Res,2007,67(13):6092-6099.
  • 7Kutay H,Bai S,Datta J,et al.Downregulation of miR-122 in the rodent and human hepatocellular carcinomas.J Cell Biochem,2006,99(3):671-678.
  • 8Michael MZ,O' Connor SM,van Holst Pellekaan NG,et al.Reduced accumulation of specific microRNAs in colorectal neoplasia.Mol Cancer Res,2003,1(12):882-891.
  • 9Cimmino A,Calin GA,Fabbri M,et al.CM.MiR-15 and miR-16 induce apoptosis by targeting BCL2.Proc Natl Acad Sci USA,2005,102 (39):13944-13949.
  • 10Cummins JM,He Y,Leary RJ,et al.The colorectal micro RNAome.Proc Natl Acad Sci USA,2006,103(10):3687-3692.

共引文献34

同被引文献46

引证文献5

二级引证文献2

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