期刊文献+

胃癌组织中miR-222与TIMP3的表达及临床意义 被引量:12

Expression and Clinical Significance of MiR-222 and TIMP3 in Gastric Cancer
暂未订购
导出
摘要 目的:探讨miR-222(Homo sapiens miR-222)与基质金属蛋白酶抑制因子3(Tissue inhibitor of metalloproteinases-3,TIMP3)在胃癌组织中的表达及其临床意义。方法:分别运用原位杂交、免疫组化检测胃癌组织及癌旁组织中miR-222与TIMP3的表达水平,分析miR-222、TIMP3之间的相关性以及与胃癌临床病理参数的关系。结果:原位杂交检测显示,在62例胃癌组织中miR-222阳性表达率为86.67%,与癌旁对照组22.58%比较,差异有统计学意义(P<0.01)。免疫组化结果显示,在62例胃癌组织中TIMP3阳性表达率为19.35%,与癌旁对照组75.81%比较,差异有统计学意义(P<0.01)。相关性分析表明,miR-222的表达与TIMP3的表达呈负相关(P<0.05);光密度值检测发现,miR-222的表达随着胃癌临床分期和浸润深度的演进而增加,且胃癌中有淋巴结转移的miR-222的表达显著高于无淋巴结转移组(P<0.01);TIMP3的表达随着胃癌临床分期和浸润深度的演进而下调,胃癌中有淋巴结转移的TIMP3的表达均显著低于无淋巴结转移组(P<0.01)。结论:在胃癌组织中高表达的miR-222和TIMP3蛋白低表达可能是胃黏膜恶性转变以及胃癌发生浸润转移的重要生物学标志,检测miR-222和TIMP3对预测结肠癌浸润转移有重要意义。 Objective: To investigates the expression of miR-222 and TIMP3 in gastric cancer, as well as their clinical significance. Methods: In situ hybridization and immunohistochemistry were used to detect the expression of miR-222 and TIMP3 in gastric cancer specimens, respectively. The correlations among the miR-222, TIMP3 protein, and clinicopathological parameters of gastric cancer were analyzed. Results: In situ hybridization showed that the positive expression rate of miR-222 was 86.67 % and 22.58 % in gastric cancer and the adjacent tissue, respectively. In the assay of immunohistochemistry, the positive expression rate of TIMP3 was 19.35 % and 75.81% in gastric cancer and the adjacent tissue, respectively. Significant differences ( P 〈 0.01 ) were found between the two aforementioned groups. The correlation analysis indicated that the expression of miR-222 had a close negative correlation with that of TIMP3 in gastric cancer ( P 〈 0.01 ). The up-regulation of miR-222 expression was associated with an advanced clinical stage, infil- trating depth, and lymph node metastasis in the cancer ( P 〈 0.01 ). Conversely, the down-regulation of the TIMP3 expression was associated with an advanced clinical stage, infiltrating depth, and lymph node metastasis in the cancer ( P 〈 0.01 ). Conclusion: The high expression of miR-222 and the low expression of the TIMP3 protein may be important biological markers for malignant transformation in the invasion and metastasis of gastric cancer. The detection of miR-222 and TIMP3 expression in gastric cancer is significantly important for improving the prediction of invasion and metastasis.
出处 《中国肿瘤临床》 CAS CSCD 北大核心 2012年第4期194-196,200,共4页 Chinese Journal of Clinical Oncology
基金 国家自然科学基金(编号:31100935 81101526)资助~~
关键词 微小RNA基质金属蛋白酶抑制因子3 胃癌临床意义 MiR-222 TIMP3 protein Gastric cancer
  • 相关文献

参考文献11

  • 1Wong QW,Ching AK,Chan AW,et al.MiR-222 overexpression confers cell migratory advantages in hepatocellular carcinoma through enhancing AKT signaling[J].Clin Cancer Res,2010,16(3):867-875.
  • 2Chun-Zhi Z,Lei H,An-Ling Z,et al.MicroRNA-221 and mi-croRNA-222 regulate gastric carcinoma cell proliferation and radio-resistance by targeting PTEN[J].BMC Cancer,2010,10:367.
  • 3Galardi S,Mercatelli N,Farace MG,et al.NF-kappa B and c-Jun induce the expression of the oncogenic miR-221 and miR-222 in prostate carcinoma and glioblastoma cells[J].Nucleic Acids Res,2011,39(9):3892-3902.
  • 4R(o)hrs S,Dirks WG,Meyer C,et al.Hypomethylation and expres-sion of BEX2,IGSF4 and TIMP3 indicative of MLL translocations in acute myeloid leukemia[J].Mol Cancer,2009,8:86.
  • 5Masson D,Rioux-Leclercq N,Fergelot P,et al.Loss of expression of TIMP3 in clear cell renal cell carcinoma[J].Eur J Cancer,2010,46(8):1430-1437.
  • 6Garofalo M,Di Leva G,Romano G,et al.miR-221-222 regulate TRAIL resistance and enhance tumorigenicity through PTEN and TIMP3 downregulation[J].Cancer Cell.2009,16(6):498-509.
  • 7Lu J,Getz G,Miska EA,et al.MicroRNA expression profiles classi-fy human cancers[J].Nature,2005,435(7043):834-838.
  • 8Rigoutsos I,Furnari F.Gene-expression forum:Decoy for microR-NAs[J].Nature,2010,465(7301):1016-1017.
  • 9Zhang L,Deng T,Li X,et al.microRNA-141 is involved in a na-sopharyngeal carcinoma-related genes network[J].Carcinogenesis,2010,31(4):559-566.
  • 10Deng X,Bhagat S,Dong Z,et al.Tissue inhibitor of metalloprotein-ase-3 induces apoptosis in prostate cancer cells and confers increased sensitivity to paclitaxel[J].Eur J Cancer.2006,42(18):3267-3273.

二级参考文献2

共引文献32

同被引文献98

  • 1胃癌诊疗规范(2011年版)[J].中国医学前沿杂志(电子版),2012,4(5):62-71. 被引量:249
  • 2顾莹莹,刘芳,陈国勤,刘慕嫦,胡帅尔,莫明聪,林云恩.非小细胞肺癌MMP-s和TIMP-s的表达与转移及预后分析[J].中国热带医学,2006,6(11):1949-1952. 被引量:7
  • 3Tomoe Lu,Hiroshi Hano,Keisuke Nagatsuma,Satoru Chiba,Masahiro Ikegami.Frequent loss of heterozygosity in two distinct regions,8p23.1 and 8p22, in hepatocellular carcinoma[J].World Journal of Gastroenterology,2007,13(7):1090-1097. 被引量:12
  • 4Ghanta KS, Li DQ, EswaranJ, et al. Gene profiling of MTAI identifies novel gene targets and functions[J]. PLoS One,20ll ,6(2) :eI7135.
  • 5Wilting SM, van Boerdonk RA, Henken FE, et al. Methylation?mediated silencing and tumour suppressive function of hsa?miR-124 in cervical cancer[J]. Mol Cancer ,2010 ,9(1) : 167.
  • 6Furuta M, Kozaki KI, Tanaka S, et al. miR -124 and miR- 203 are epigenetically silenced tumor-suppressive mi?croRNAs in hepatocellular carcinoma[J]. Carcinogene?sis,2010,31(5) :766-776.
  • 7Li KK, PangJC, Ching AK, et al. miR-124 is frequently down-regulated in medulloblasto and is a negative regula?tor of SLCI6AI[J]. Hum Pathol,2009,40(9) :1234-1243.
  • 8PiersonJ, Hostager B, Fan R, et al. Regulation of cyclin dependent kinase 6 by microRNA 124 in medulloblas?toma[J].J Neurooncol ,2008 ,90( I ) : 1-7.
  • 9Hunt S,Jones AV,Hinsley EE,etal. MicroRNA-124 sup?presses oral squamous cell carcinoma motility by targeting ITGBI[J]. FEBS Lett ,2011,585 (1) : 187 -192.
  • 10SilberJ, Lim DA, Petritsch C, et al. miR-124 and miR- 137 inhibit proliferation of glioblastoma multi forme cells and induce differentiation of brain tumor stem cells[J] . BMC Med ,2008,6: 14.

引证文献12

二级引证文献37

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