期刊文献+

三氧化二砷诱导子宫内膜癌细胞凋亡的研究 被引量:2

The molecular mechanism of the apoptosis in endometrial carcinoma cells induced by As_2O_3
下载PDF
导出
摘要 目的在体外实验中,探讨三氧化二砷(As2O3)诱导子宫内膜癌细胞发生凋亡的可能性,揭示该凋亡发生与bcl-2和bax之间的关系。方法采用TUNEL染色法,定性、定量地研究As2O3与子宫内膜癌细胞凋亡的关系;通过免疫组织化学法检测凋亡相关基因bcl-2和bax的表达。结果As2O3在体外能诱导子宫内膜癌细胞发生凋亡,下调bcl-2的表达,增强bax的表达。结论诱导子宫内膜癌细胞发生凋亡是As2O3抗子宫内膜癌作用的机制之一,As2O3可能通过下调bcl-2的表达及增强bax的表达诱导子宫内膜癌细胞发生凋亡。 Objective To investigate the apoptosis in endometrial carcinoma cells induced by As2O3, and the expression of bcl-2 and bax. Methods In vitro experiments, TUNEL staining method was used to quantitatively and qualitively detect the apoptosis status of endometrial carcinoma cells HEC-1A before and after the As2O3 treatment. Immunohistochemical staining was used to detect the expression of apoptosis-regulated gene bcl-2 and bax. Results As2O3 was able to induce the apoptosis in endometrial carcinoma cells. As2O3 can reduce the expression of apoptosis-regulated gene bcl-2, and up-regulate the expression of apoptosis-regulated gene bax. Conclusions As2O3 was able to induce the apoptosis in endometrial carcinoma cells. This apoptosis may be mediated by down-regulation of apoptosis-regulated gene bcl-2 and up-regulation of bax.
出处 《解放军保健医学杂志》 2006年第1期36-38,共3页 Journal Of Health Care And Medicine in Chinese Pla
关键词 子宫内膜癌 细胞凋亡 三氧化二砷类 endometrial carcinoma apoptosis As2O3
  • 相关文献

参考文献6

  • 1[1]Creutzberg CL,van Putten WL,Koper PC,et al.Survival after relapse in patients with endometrial cancer:results from a randomized trial[J].Gynecol Oncol,2003,89:201-209
  • 2[2]Bellamy CO,Malcomson RD,Harrison DJ,et al.Cell death in health and disease:the biology and regulation of apoptosis[J].Sem Cancer Biol,1995,6:3-16
  • 3[3]Cai X,SHen YL,ZHu Q,et al.Arsenic trioxide-induced apoptosis and differentiation are associated respectively with mitochondrial transmembrane potential collapse and retinoic acid signaling pathways in acute promyelocytic leukemia[J].Leukemia,2000,14:262-270
  • 4高虎,赵治华,杨峰.三氧化二砷诱导细胞凋亡治疗消化道肿瘤的研究[J].世界华人消化杂志,2002,10(6):710-711. 被引量:9
  • 5[5]Oltvai ZN,Milliman CL,Korsmeyer SJ.Bcl-2 heterodimerizes in vivo with a conserved homolog,Bax,that accelerates programmed cell death[J].Cell,1993,74:609-619
  • 6[6]Yang E,Zha J,Jockel J,et al.Bad,a heterodimeric partner for Bcl-XL and Bcl-2,displaces bax and promotes cell death[J].Cell,1995,80:285-291

二级参考文献23

共引文献8

同被引文献27

引证文献2

二级引证文献7

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