Review -: Induction of prostate apoptosis by α1-adrenoceptor antagonists:: mechanistic significance of the quinazoline component

被引:66
作者
Anglin, IE
Glassman, DT
Kyprianou, N
机构
[1] Univ Maryland, Med Ctr, Div Urol, Dept Surg,Sch Med, Baltimore, MD 21201 USA
[2] Univ Maryland, Sch Med, Dept Mol Biol & Biochem, Baltimore, MD 21201 USA
关键词
prostate; apoptosis; adrenoceptor antagonist; quinazoline; TGF-beta;
D O I
10.1038/sj.pcan.4500561
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
alpha(1)-Adrenoceptor antagonists, have been documented to induce apoptosis and reduce prostate tumor vascularity in benign and malignant prostate cells. The quinazoline based alpha(1)-antagonists, doxazosin and terazosin but not tamsulosin (a sulphonamide derivative) suppress prostate growth without affecting cell proliferation. These quinazoline-mediated apoptotic effects occur via an alpha(1)-adrenoceptor independent mechanism potentially involving activation of the TGF-beta signal transduction pathway. This review discusses the current knowledge of the action of quinazoline-derived alpha(1)-adrenoceptor antagonists in the benign and malignant prostate and their potential therapeutic use in the treatment of benign prostatic hyperplasia (BPH) and prostate cancer. Finally, a molecular pathway is proposed for their observed apoptotic function against prostate cells. Increased understanding of the action of these established and clinically accepted agents would provide a basis for the design of safe, effective therapeutic regimens in the treatment of prostatic diseases.
引用
收藏
页码:88 / 95
页数:8
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