期刊文献+

Recent progress in the study of methylated tumor suppressor genes in gastric cancer 被引量:4

Recent progress in the study of methylated tumor suppressor genes in gastric cancer
下载PDF
导出
摘要 Gastric cancer is one of the most common malignancies and a leading cause of cancer mortality worldwide.The pathogenesis mechanisms of gastric cancer are still not fully clear.Inactivation of tumor suppressor genes and activation of oncogenes caused by genetic and epigenetic alterations are known to play significant roles in carcinogenesis.Accumulating evidence has shown that epigenetic silencing of the tumor suppressor genes,particularly caused by hypermethylation of CpG islands in promoters,is critical to carcinogenesis and metastasis.Here,we review the recent progress in the study of methylations of tumor suppressor genes involved in the pathogenesis of gastric cancer.We also briefly describe the mechanisms that induce tumor suppressor gene methylation and the status of translating these molecular mechanisms into clinical applications. Gastric cancer is one of the most common malignancies and a leading cause of cancer mortality worldwide. The pathogenesis mechanisms of gastric cancer are still not fully clear. Inactivation of tumor suppressor genes and activation of oncogenes caused by genetic and epigenetic alterations are known to play significant roles in carcinogenesis. Accumulating evidence has shown that epigenetic silencing of the tumor suppressor genes, particularly caused by hypermethylation of CpG islands in promoters, is critical to carcinogenesis and metastasis. Here, we review the recent progress in the study of methylations of tumor suppressor genes involved in the pathogenesis of gastric cancer. We also briefly describe the mechanisms that induce tumor suppressor gene methylation and the status of translating these molecular mechanisms into clinical applications.
出处 《Chinese Journal of Cancer》 SCIE CAS CSCD 2013年第1期31-41,共11页
基金 supported by grants from National Natural Science Foundation of China(No.30770920 and 81071651) Zhejiang Provincial Natural Science Foundation of China(No.R2100213,2009C33142,Z2090056 and WKJ2009-2-028) 973 Project(No.2010CB834300)
关键词 抑癌基因 甲基化 胃癌 肿瘤抑制基因 癌组织 发病机制 表观遗传 恶性肿瘤 Gastric cancer, methylation, tumor suppressor genes, epigenetics
  • 相关文献

参考文献4

二级参考文献215

  • 1[1]Tamura G,Kihana T,Nomura K,Terada M,Sugimura T,Hirohashi S.Detection of frequent p53 gene mutations in primary gastric cancer by cell sorting and polymerase chain reaction single-strand conformation polymorphism analysis.Cancer Res 1991; 51:3056-3058
  • 2[2]Becker KF,Atkinson MJ,Reich U,Becker I,Nekarda H,Siewert JR,Hofler H.E-cadherin gene mutations provide clues to diffuse type gastric carcinomas.Cancer Res 1994; 54:3845-3852
  • 3[3]Tamura G,Sakata K,Nishizuka S,Maesawa C,Suzuki Y,Iwaya T,Terashima M,Saito K,Satodate R.Inactivation of the E-cadherin gene in primary gastric carcinomas and gastric carcinoma cell lines.Jpn J Cancer Res 1996; 87:1153-1159
  • 4[4]Kim IJ,Kang HC,Shin Y,Park HW,Jang SG,Han SY,Lim SK,Lee MR,Chang HJ,Ku JL,Yang HK,Park JG.A TP53-truncating germline mutation (E287X) in a family with characteristics of both hereditary diffuse gastric cancer and LiFraumeni syndrome.J Hum Genet 2004; 49:591-595
  • 5[5]Guilford P,Hopkins J,Harraway J,McLeod M,McLeod N,Harawira P,Taite H,Scoular R,Miller A,Reeve AE.E-cadherin germline mutations in familial gastric cancer.Nature 1998; 392:402-405
  • 6[6]Tamura G,Yin J,Wang S,Fleisher AS,Zou T,Abraham JM,Kong D,Smolinski KN,Wilson KT,James SP,Silverberg SG,Nishizuka S,Terashima M,Motoyama T,Meltzer SJ.E-Cadherin gene promoter hypermethylation in primary human gastric carcinomas.JNatl Cancer Inst 2000; 92:569-573
  • 7[7]Nishizuka S,Tamura G,Terashima M,Satodate R.Loss of heterozygosity during development and progression of differentiated adenocarcinoma of the stomach.J Pathol 1998;185:3843
  • 8[8]Akiyama Y,Nakasaki H,Nihei Z,Iwama T,Nomizu T,Utsunomiya J,Yuasa Y.Frequent microsatellite instabilities and analyses of the related genes in familial gastric cancers.Jpn J Cancer Res 1996; 87:595-601
  • 9[9]Semba S,Yokozaki H,Yasui W,Tahara E.Frequent microsatellite instability and loss of heterozygosity in the region including BRCA1 (17q21) in young patients with gastric cancer.Int J Oncol 1998; 12:1245-1251
  • 10[10]Tamura G,Sakata K,Maesawa C,Suzuki Y,Terashima M,Satoh K,Sekiyama S,Suzuki A,Eda Y,Satodate R.Microsatellite alterations in adenoma and differentiated adenocarcinoma of the stomach.Cancer Res 1995; 55:1933-1936

共引文献152

同被引文献7

引证文献4

二级引证文献1

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