›› 2012, Vol. 43 ›› Issue (1): 59-62.doi: 10.3969/j.issn.0529-1356.2012.01.011

• 肿瘤生物学 • 上一篇    下一篇

3-甲基腺嘌呤对顺铂诱导HeLa细胞凋亡的影响

徐冶1; 李质馨; 1*; 曹慧玲2; 刘洪梅2; 于洋2; 刘师兵2; 方青2; 王晓军2   

  1. 1.吉林医药学院组织学胚胎学教研室;2.医学科研实验室,吉林 吉林市132013
  • 收稿日期:2011-04-22 修回日期:2011-06-20 出版日期:2012-02-06
  • 通讯作者: 李质馨

Effect of 3-methyladenine on cisplatin induced-apoptosis of line HeLa cells

  1. 1. Department of Histology and Embryology, Jilin Medical College,Jilin Jilin 132013, China; 2.Medical Research Laboratory,Jilin Medical College,Jilin Jilin 132013, China
  • Received:2011-04-22 Revised:2011-06-20 Online:2012-02-06
  • Contact: LI Zhi-xin

关键词: 3-甲基腺嘌呤, 顺铂, 宫颈癌, 自噬, HeLa细胞, 间接免疫荧光法

Abstract: Objective Autophagy is a protective reaction when cells are under stress, but the effect of autophagy in cisplatin induced apoptosis is unclear. The objective of this study is to investigate the effect of autophagy on cisplatin induced apoptosis of HeLa cells using autophagy specific inhibitor 3-methyladenine. BR> Methods MTT assay was employed to examine the growth suppression of the cells. Inverted phase contrast microscope was used to detect the morphological changes of the cells. Indirect immunofluorescence was used to dectect the expression and location of the LC3 and p62 proteins. Hoechst staining was used to observe the apoptosis. Results MTT assay showed that 3-Methyladenine combined with DDP enhanced the growth inhibition effect of cisplatin on HeLa cell line. Under the inverted phase contrast microscope, the cells became more round and fragile with the usage of 3-methyladenine and cisplatin. Indirect immunofluorescence staining showed that 3-methyladenine combined with DDP inhibited the expression and colocalization of LC3 and p62 Hoechst staining showed that 3methyladenine combined with DDP enhanced the apoptosis of HeLa cells induced by cisplatin. Conclusion Inhibition of the autophagy by 3-methyladenine enhances the apoptosis induced by cisplatin in

Key words: 3-methyladenine, Cisplatin, Cervical cancer, Autophagy, HeLa cell, Indirect immunofluorescence

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