Testosterone induced apoptosis in colon cancer cells is regulated by PI3K/Racl signaling

作     者：Saad Alkahtani 

作者机构：Department of Zoology Science College King Saud University Riyadh 11352 Saudi Arabia 

出 版 物：《Asian Journal of Andrology》 (亚洲男性学杂志（英文版）)

年 卷 期：2013年第15卷第6期

页      面：831-834,I0011页

核心收录：

学科分类：10[医学] 

基　　金：the Deanship of Scientific Research at King Saud University for funding this study through research 

主　　题：actin apoptosis colon cancer cell testosterone 

摘      要：Recently, it has been reported that testosterone membrane signaling regulates actin reorganization and induces pro-apoptotic responses in colon tumor cells. In the present study the membrane androgen receptors （mARs）-induced activation of Rac I GTPase and the involvement of PI3K/Racl signaling in controlling the apoptotic responses in testosterone treated Caco2 colon cancer cells has been analyzed. In line with previous findings, activation of mAR by testosterone conjugates triggered early and transient actin reorganization as indicated by the significant decrease of the G/Total actin ratio after 15- and 30-min treatment of the cells. Interestingly, stimulation of mAR rapidly activated the Racl GTPase. This effect was evident after 15 min and persisted for at least 24 h. Testosterone induced Rac I activation was fully blocked in Caco2 cells pre-treated with the PI3K inhibitor wortmannin, indicating that Racl signaling is acting downstream of the PI3K pathway. Remarkably, when cells were pre-treated with wortmannin that blocks the PI3K/Racl signaling, apoptotic response was almost fully inhibited. These finding suggest that Racl activation, triggering actin redistribution, is involved in testosterone induced pro-apoptotic responses governed by mAR activation and emphasize the regulatory role of PI3K/Racl signaling in colon tumors.