期刊文献+

组蛋白甲基转移酶基因G9a在肝外胆管癌组织中转录表达及其临床意义的研究 被引量:1

Transcriptional expression of histone methyltransferase gene G9a and its clinical significance in extrahepatic cholangiocarcinoma
原文传递
导出
摘要 目的探讨组蛋白甲基转移酶基因G9a在肝外胆管癌中的表达及其临床意义。方法用RT-PCR的方法检测48例肝外胆管癌组织及39例癌旁对照组织中C9a mRNA的表达,并分析其阳性表达率与临床病理因素之间的相关性。结果G9a在肝外胆管癌组织中的转录表达率为56.25%(27/48),明显高于对照组织并与肝外胆管癌的淋巴转移及TNM分期(P〈0.05)相关。结论组蛋白甲基转移酶基因G9a在胆管癌组织中表达上调,提示由G9a引起的组蛋白甲基化紊乱在肝外胆管癌的发生发展中发挥重要作用。 Objective To investigate the transcriptional expression of histone methyltransferase gene Gga and its clinical significance in extrahepatic cholangiocarcinoma. Methods The mRNA of Gga was detected by RT-PCR in 48 extrahepatic cholangiocarcinomas and 39 contral tissues. Results The frequency of transcriptional expression of Gga in extrahepatic cholangiocarcinoma was 56. 25% (27/ 48) ,and it was higher than that in the control and positively correlated with lymph metastasis and TNM stage (P〈0.05). Conclusion The significant difference in expression of G9a between tumor and control implicated the important roles of histone methylation disruption resulted from increased Gga expression in extrahepatic cholangiocarcinoma.
出处 《中华肝胆外科杂志》 CAS CSCD 2007年第7期460-462,共3页 Chinese Journal of Hepatobiliary Surgery
基金 国家高技术研究发展计划(863计划)资金资助项目(2002AA214061)
关键词 胆管肿瘤 肝外胆管癌 组蛋白甲基转移酶 G9a Bile duct neoplasms Extrahepatic cholangiocarcinoma Histone methyltransferase Gga
  • 相关文献

参考文献12

  • 1Rea S, Eisenhaber F, O'Carroll D, et al. Regulation of chromatin structure by site-specific hitone H3 methyltransferase. Nature, 2000, 406: 593-599.
  • 2Rong W, Anna VT, Prim B, et al. Differential subnuclear localization and replication timing of histone H3 lysine 9 methyl ation states. Mol Biol Cell, 2005, 16: 2872-2881.
  • 3Tachbana M, Sugimoto K, Fukushima T, et al. Set domaincontaining protein, G9a, is a novel lysine-preferring mammalian histone methyltransferase with hyperactivity and specific selectivity to lysines 9 and 27 of histone H3. J Biol Chem, 2001, 276: 25309-25317.
  • 4Debasis P, Hang GC, Pierre-Olivier E, et al. Substrate specificity and kinetic mechanism of mammalian Gga histone H3 methytransferase. J Biol Chem, 2004, 279:53248-53258.
  • 5Tachibana M, Sugimoto K, Nozaki M, et al. G9a histone methyltransferase plays a dominant role in euehromatie histone H3 lysine 9 methylation and is essential for early embryogenesis. GenesDev, 2002, 16: 1779-1791.
  • 6Feldman N, Gerson A, Fang J, et al. G9a-mediated irreversible epigenetic inactivation of Oct-3/4 during early embryogenesis. Nat Cell Biol, 2006, 8: 188-194.
  • 7Xin Z, Tachibana M, Guggiari M, et al. Role of histone methyltransferase Gga in CpG methylation of the Prader-Willi syndrone imprinting center. J Biol Chem, 2003, 278: 14996- 15000.
  • 8Lee DY, Northrop JP, Kuo MH, et al. Histone H3 lysine 9 methyltransferase G9a is a transcriptional coactivator for nuclear receptors. J Biol Chem, 2006, 281: 8476-8485.
  • 9Nishio H, Walsh MJ. CCAAT displacement protein/cut homolog recruits G9a histone lysine methyltransferase to repress transcription. Proc Natl Acad Sci USA, 2004, 101:11257-11262.
  • 10Silva J, Mak W, Zvetkova I, et al. Establishment of histone h3 methylation on the inactive Ⅹ chromosome requires transient recruitment of Eed-Enxl polycomb group complexes. Dev Cell, 2003, 4:481-495.

同被引文献4

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