期刊文献+

5-脱氧杂氮胞苷调控p16基因表达对人宫颈癌HeLa细胞增殖及调亡的影响 被引量:1

Effects of 5-Aza-CdR on proliferation and apoptosis by modulating p16 gene expression in human cervical carcinoma cell line HeLa
下载PDF
导出
摘要 目的:探讨甲基化转移酶抑制剂5-脱氧杂氮胞苷(5-Aza-CdR)对人宫颈癌HeLa细胞增殖和调亡的作用及其可能机制。方法:应用不同浓度的5-Aza-CdR处理HeLa细胞,甲基化特异PCR(MSP)法检测处理前后p16基因甲基化状态,应用RT-PCR方法检测p16基因mRNA表达,MTT法检测细胞增殖,流式细胞术检测细胞凋亡率。结果:人宫颈癌HeLa细胞p16基因启动子区呈高甲基化状态,经过5-Aza-CdR处理后,p16基因启动子区呈去甲基化状态,其mRNA重新表达,细胞生长受到抑制,细胞凋亡增加。结论:5-Aza-CdR能够逆转p16基因甲基化状态,调控p16基因表达,并有效抑制人宫颈癌HeLa细胞的增殖和诱导细胞调亡。 Objective:To investigate the effects of 5-aza-2-deoxycytidine(5-Aza-CdR) on proliferation and apoptosis in human cervical carcinoma cell line HeLa and the possible mechanism.Methods: HeLa cells was treated with different concentration of DNA methytransferase inhibitor 5-Aza-CdR.Methylation-specific polymerase chain reaction(MSP) was used to detect promoter methylation status of p16 gene and RT-PCR was used to detect re-expression of mRNA.Cell growth was estimated by MTT assay and cell apoptosis rate was determined by flow cytometry.Results: Promoter hypermethylation of the p16 gene was detected in HeLa cells.After treatment with 5-Aza-CdR,the promoter region of the p16 gene exhibited a demethylation status,and the p16 gene mRNA was re-expressed.The cellular growth activity decreased and cell apoptosis increased.Conclusion: The 5-Aza-CdR could reverse the methylation of p16 gene to regulate the expression of p16 gene,and could effectively inhibit the cellular proliferation and induce apoptosis of cervical carcinoma cells.
出处 《西北国防医学杂志》 CAS 2012年第2期110-113,共4页 Medical Journal of National Defending Forces in Northwest China
关键词 宫颈肿瘤 5-脱氧杂氮胞苷 P16基因 甲基化 Cervix neoplasms 5-Aza-CdR p16 gene Methylation
  • 相关文献

参考文献1

二级参考文献11

  • 1Herman J G,Graff J R,Myohanen S.Methylation-specific PCR:a novel PCR assay for methylation status of CpG island.Proc Natl Acad Sci USA,1996,93(18):9821~9826. 被引量:1
  • 2Fan X,Inda M M,Tunnon T.Improvement of the methylation specific PCR technical conditions for the detection of p16 promoter hypermethylation in small amounts of tumor DNA.Oncol Rep,2002,9(1):181~183. 被引量:1
  • 3NoboriT,Miura K,Wu D T.Deletion of the cyclindepent kinase 4 inhibitor gene in mutiple human cancers.Nature,1993,368~753. 被引量:1
  • 4HermanJ G,Merlu A,Mao L.Inactivation of the CDKN2/p16/MTS1 gene is frequently associated with abberant DNA methylation in all common human cancers.Cancer Res.,1995,55:4525~4530. 被引量:1
  • 5Bird A P.CpG-rich-island,and the function of DNA methylation.Nature, 1986,321(15):209~213. 被引量:1
  • 6Tycko B.Epigenetic gene silencing in cancer.J clin Invest.2000,105(4):401~407. 被引量:1
  • 7Wong Y F,Chung T K, Cheung T H.p16INK4A and p15INK4B alterations in primary gyneclogic malignancy.Gynecol Oncol,1997, 65:319~324. 被引量:1
  • 8Virmani A K,Muller C,Rathi A.Aberrant methylation during cervical carcinogenesis.Clin Cancer Res,2001,7(3):584~589. 被引量:1
  • 9Dong S M,Kim H S,Rha S H.Promoter hypermethylation of multiple genes in carcinoma of the uterine cervix.Clin Cancer Res,2001,7:1982~1986. 被引量:1
  • 10Wang H,Ma H U.Expression and significance of p16 protein in cervical cancer.Modern Gynecology and Obstetric Progress, 1998,7(1):11~14. 被引量:1

共引文献12

同被引文献13

引证文献1

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