期刊文献+

大肠癌MTS基因突变和p16蛋白表达

The Mutation of MTS Gene and Expression of p16 Protein in Colorectal Cancer
暂未订购
导出
摘要 [目的]分析大肠癌MTS基因突变与 p16蛋白表达的关系。[方法]应用PCR -SSCP技术及LSAB免疫组织化学法同时检测135例大肠癌MTS基因的突变和其基因产物(p16蛋白)的表达情况。[结果]135例大肠癌MTS基因的突变率为4.44% ,与正常粘膜组织相比差异并无显著性 ,p16蛋白阳性率为59.25% ,与正常粘膜组织相比有显著性差异(P<0.05)。[结论]大肠癌极少发生MTS基因突变 ,但有较高的 p16蛋白表达下调。MTS基因表达障碍可能有另外原因。 To investigate the mutation of MTS gene and the expression of p16 protein,which may have a great effect on the carcinogensis of colorectum.PCR SSCP technology was used to detected the mutation of MTS gene with a primer of exon 2 of MTS gene,and the expression of its product p16 protein was detected using LSAB immunohistochemical method in 135 cases with colorectal cancer.The mutation rate of MTS gene of 135 cases with colorectal cancer was 4.44%.Although there was no difference between colorectal cancer and normal mucous membranes for mutation rate of MTS gene,it was founded that there was a significant difference in the expression of p16 protein between two groups (the positive rate of p16 was 59.26% in colorectal cancer versus 100% in normal tissues).[Conclusion]The mutation of MTS gene in colorectal cancer is not common,however,the expression of p16 protein is much lower.There must be an another regular mechanism controlling p16 protein synthesis which may be one of factors of the carcinogenesis in colorectal cancer.
出处 《中国肿瘤》 CAS 2001年第8期488-489,共2页 China Cancer
基金 山东省科研基金资助 (961165308)
关键词 结直肠肿瘤 MTS基因 P16蛋白 colorectal neoplasms MTS gene p16 protein
  • 相关文献

参考文献8

  • 1[1]Vander Riet P,Nawtoz H,Hruban RH,et al.Frequent loss of chromosome qp21-22early in head and neck cancer progression[J].Cancer Ras,1994;54:1156.
  • 2[2]Kmb A,Gruis NA,Weaver-Feldhaus J,et al.A cell cycle regulatorpotentially involved in genesis of many tumortypes[J].Science,1994,264:437.
  • 3[3]Noborl T,Mlura K,Wu DJ,et al.Deletions of the cvclin development kinase-4inhibitor gene in multiple human cancer[J].Nature,1994,368:735-736.
  • 4[4]Marx J.New tumor supperessor may rival p53[J].Science,1994,264:344-345.
  • 5[5]Moulton T,Samara G,Chuna WY,et al.MTS1/p16/CDKN2 Lesions in priamryglioblastoma multiform[J].Am J Pathol,1995,146:613.
  • 6[6]Okamoto A,Demetrick DJ,Spillare EA,et al.Mutation and altered expression ofp16 INK4 in human cancer[J].Proc Natl Acad Sci USA,1994,91:11045-11049.
  • 7[7]Spillare EA,Odamoto A,Hagiwra K,et al.Supperssion of growth in vitro andtumorigencity in vivo of human carcinoma cell lines by transfected P16ink4[J].Mol Carcinog,1996,16:53-60.
  • 8[8]Jen J,Harper W,Bigner SH,et al.Delection of p16 and p16 genes in braintumors[J].Cancer Res,1994,54:6353-6358.

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