Naftopidil, a selective α-1 adrenoceptor antagonist, inhibits growth of human prostate cancer cells by G1 cell cycle arrest

被引:59
作者
Kanda, Hideki [1 ]
Ishii, Kenichiro [1 ]
Ogura, Yuji [1 ]
Imamura, Tetsuya [1 ]
Kanai, Masahiro [1 ]
Arima, Kiminobu [1 ]
Sugimura, Yoshiki [1 ]
机构
[1] Mie Univ, Grad Sch Med, Dept Nephro Urol Surg & Androl, Tsu, Mie 5148507, Japan
关键词
prostate cancer; naftopidil; cell cycle;
D O I
10.1002/ijc.23095
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
alpha-1 adrenoceptor antagonists are generally prescribed for benign prostate hyperplasia with lower urinary tract symptoms. Naftopidil, a selective a-1 adrenoceptor antagonist, is frequently used in Japan because it has fewer side effects. Here we demonstrate for the first time that naftopidil has growth inhibitory effect in androgen-sensitive and -insensitive human prostate cancer cell lines. The concentrations causing 50% inhibition (IC50) of cancer cell growth were 22.2 +/- 4.0 mu M in androgen -sensitive LNCaP cells and 33.2 +/- 1.1 mu M in androgen-insensitive PC-3 cells. FACS analysis revealed that cell growth inhibition by naftopidil was due to the arrest of the G1 cell cycle. Expressions of p27(kip1) and p21(cip1) were significantly increased in LNCaP cells treated with naftopidil. In PC-3 cells, naftopidil induced p21(cip1) but not p27(kip1) In vivo, oral administration of naftopidil to nude mice inhibited the growth of PC-3 tumors as compared to vehicle-treated controls. These results suggest that naftopidil may be useful in the chemoprevention of prostate cancer and the intervention of hormone refractory prostate cancer. (c) 2007 Wiley-Liss, Inc.
引用
收藏
页码:444 / 451
页数:8
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