首都医科大学学报 ›› 2004, Vol. 25 ›› Issue (2): 250-252.

• 论著·临床研究 • 上一篇    下一篇

米非司酮对雄激素非依赖性前列腺癌LNCaPC4-2和PC3细胞的作用机制

毕泗成, 徐秀红, 邵强, 杜林栋   

  1. 首都医科大学附属北京友谊医院泌尿科
  • 收稿日期:2003-04-15 修回日期:1900-01-01 出版日期:2004-04-15 发布日期:2004-04-15

Inhibiting Mechanism of Mifepristone on Androgen-Independent Prostate Cancer Cell Lines LNCaPC4-2,PC3 in Vitro

Bi Sicheng, Xu Xiuhong, Shao Qiang, Du Lindong   

  1. Dept. of Urology, Beijing Friendship Hospital, Affiliate of Capital University of Medical Sciences
  • Received:2003-04-15 Revised:1900-01-01 Online:2004-04-15 Published:2004-04-15

摘要: 为探讨抗孕激素药米非司酮对雄激素非依赖性前列腺癌细胞株LNCaPC4-2、PC3的促凋亡及生长抑制作用,将不同浓度的米非司酮加入到体外培养的2株前列腺癌细胞中,分别在培养后3 d、5 d、7 d用SRB染色法检测细胞生长抑制率;用流式细胞仪检测加药后24 h、48 h LNCaPC4-2和PC3细胞凋亡情况.发现:高浓度米非司酮(20 μmol/L)对雄激素非依赖性细胞株LNCaPC4-2、PC3于3 d、5 d、7 d的细胞生长抑制率分别为55.79% 、66.37%、71.54%和87.42%、98.15%、100%.不同浓度米非司酮即2.5、5、10、15、20 μm ol/L对LNCaPC4-2、PC3细胞株7 d时的细胞生长抑制率分别为17.07%、35.77%、53.6 6% 、63.41%、71.54%和48.25%、63.42%、82.37%、95.31%、100%.前列腺癌细胞株LNCaPC4-2受15 μmol/L米非司酮作用24 h和48 h细胞凋亡率分别为19.30%、30.04%;PC3受米非司酮15 μmol/L作用24 h细胞凋亡率为44.52%.提示:米非司酮对LNCaPC4-2、PC3细胞株有时间和剂量依赖的生长抑制作用,其生长抑制作用是通过促进细胞凋亡实现的.

关键词: 米非司酮, 雄激素非依赖性, 前列腺癌, 细胞株, 凋亡

Abstract: The aim was to present our attempts on investigating the pro-apoptosis and growth suppression effects of antiprogestin mifepristone on androgen-independent prostate cancer cell lines LNCaPC4-2, PC3 in vitro. Using SRB method, the inhibition rates of different concentrations of mifepristone on the two cell lines were studied after drug 3 d, 5 d and 7 d after administration. The study also assessed the apoptosis rates induced by 15 μmol/L mifepristone on LNCaPC4-2, PC3 cell lines after 24 h, 48 h treatment. When the LNCaPC4-2 cell line and the PC3 cell line were treated with 20 μmol/L mifepristone, the corresponding rates were 55.79%, 66.37%, 71.54% and 87.42%, 98.15 %, 100% on the 3 rd day, 5 th day and 7 th day. When the two cell lines were dealt with different concentrations of mifepristone 2.5 μmol/L, 5 μmol/L, 10 μmol/L, 15 μmol/L, 20 μmol/L, the corresponding suppression rates on the 7 th day were: 17.07%, 35.77%, 53.66%, 63.41%, 71.54 % and 48.25%, 63.42%, 82.37%, 95.31 %, 100% respectively. Using flow cytometry method, the apoptosis rates of 15 μmol/L mifepristone for LNCaPC4-2 cell line were: 19.30% at 24 h and 30.04 % at 48 h, for PC3 cell line was 44.52% at 24 h. Antiprogestin mifepristone can induce apoptosis of androgen-independent prostate cancer cell lines LNCaPC4-2, PC3 in vitro. This pro-apoptosis effect is time-and-dose dependent.

Key words: mifepristone, androgen-independent, prostate cancer, cell line, apoptosis

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