基础医学与临床 ›› 2009, Vol. 29 ›› Issue (8): 855-858.

• 研究论文 • 上一篇    下一篇

孕激素促子宫内膜癌细胞株凋亡及下调细胞内survivin表达

钱素敏 王蕙兰   

  1. 沧州市中心医院
  • 收稿日期:2008-02-28 修回日期:2008-12-30 出版日期:2009-08-20 发布日期:2009-08-20
  • 通讯作者: 钱素敏

Effects of progesterone on survivin in ishikawa endometrial carcinoma cell line

Su-min QIAN, Hui-lan WANG   

  1. Central Hospital of Cangzhou
  • Received:2008-02-28 Revised:2008-12-30 Online:2009-08-20 Published:2009-08-20
  • Contact: Su-min QIAN,

摘要: 目的 观察孕酮(P)对人子宫内膜癌内膜高分化腺癌细胞株Ishikawa细胞内survivin蛋白表达的影响,探讨孕激素治疗子宫内膜腺癌的机制。方法 体外培养人子宫内膜高分化腺癌细胞株Ishikawa细胞,MTT法观察细胞的增殖;流式细胞仪(FCM)检测细胞周期和细胞凋亡率;链霉素抗生物素蛋白-过氧化物酶连接(SP)法测定Ishikawa细胞survivin蛋白的表达。结果 P呈剂量依赖性抑制Ishikawa细胞增殖(P<0.01)。P组G0/G1期细胞比例上升,S期细胞比例下降,凋亡率上升,并出现细胞凋亡峰(P<0.01)。survivin在Ishikawa细胞中有强表达, P处理24h后,明显下调survivin的表达,(P<0.01)。结论 孕酮调解调亡抑制蛋白Survivin的表达可能是调节细胞凋亡的机制之一。

关键词: 子宫内膜肿瘤, 孕酮, 增殖, 凋亡

Abstract: Objective To investigate the effects of progesterone on apoptosis and surviving expression protein of Ishikawa cell line of human endometrial carcinoma in vitro, Methods The proliferational of Ishikawa cells cultured in vitro were determined by methyl thiazolyl terazolium (MTT) medhod.Cell cycle, apoptotic percentage were detected by cytometer . The expressions of survivin protein of Ishikawa cells were detected by immunocytochemistry. Results progesterone inhibited the growth of Ishikawa cells significantly when the concentration of progesterone was at 0.5×10-5~10-4mol/l(p<0.01). Flow cytometry(FCM) showed that the proportion percentage of G0/G1 phase and the apoptotic rate were increased significantly. The proportion of S phase was reduced (p<0.01). Apoptosis morphology was observed in each group . The expression of survivin of in Ishikawa cells was lowed after the cells was treated with P. Conclusion Progesterone could inhibit the proliferation and induce apoptosis of Ishikawa cells. The regulation on the expression of the survivin protein by progesterone seems to be responsible for the effects on the apoptosis in Ishikawa cells.

Key words: Endometrial neoplasm, Progesterone, Proliferation, Apoptosis