Valproic acid induces apoptosis in prostate carcinoma cell lines by activation of multiple death pathways

被引:33
作者
Angelucci, Adriano [1 ]
Valentini, Alessandra
Millimaggi, Danilo
Gravina, Giovanni L.
Miano, Roberto
Dolo, Vincenza
Vicentini, Carlo
Bologna, Mauro
Federici, Giorgio
Bernardini, Sergio
机构
[1] Univ Aquila, Dept Expt Med, Sch Med, Via Vetoio,Coppito 2, I-67100 Laquila, Italy
[2] Univ Aquila, Dept Basic & Appl Biol, Sch Sci, I-67100 Laquila, Italy
[3] Univ Aquila, Dept Surg, Sch Med, I-67100 Laquila, Italy
[4] Univ Roma Tor Vergata, Dept Internal Med, Rome, Italy
[5] Univ Roma Tor Vergata, Dept Lab Med PTV, Rome, Italy
[6] Univ Roma Tor Vergata, Dept Urol, Rome, Italy
[7] Santa Lucia Fdn, IRCCS, Rome, Italy
[8] Bambino Gesu Pediat Hosp, IRCCS, Rome, Italy
关键词
Bcl-2; Fas; FasL; histone deacetylase; mitochondrial depolarization;
D O I
10.1097/01.cad.0000236302.89843.fc
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Valproic acid is a well-known antiepileptic drug that was recently discovered to have a wide-spectrum antitumoral action in several tumors. In our work, we tested the proapoptotic activity of valproic acid in prostate cancer. Valproic acid-induced apoptosis was described by several in-vitro assays in three prostate cancer cell lines: two representing the prototype of advanced, clinically untreatable stages of prostate progression, PC3 and DU145, and one resembling a more differentiated androgen-sensitive tumor, LNCaP. We observed that valproic acid was a potent and early apoptotic inducer, mainly in less-differentiated prostate cancer cell lines. The molecular analysis of the apoptotic machinery involved in valproic acid action revealed a central role in Bcl-2 downmodulation. When prostate cancer cells were treated for a longer time with valproic acid, we detected an enhancement of Fas-dependent apoptosis associated with an overexpression in Fas and Fas ligand. Our data indicate that the use of valproic acid may be a suitable therapeutic agent in the control of prostate cancer progression and its action appears particularly relevant in the control of refractory stages of prostate cancer. Anti-Cancer Drugs 17:1141-1150 (c) 2006 Lippincott Williams & Wilkins.
引用
收藏
页码:1141 / 1150
页数:10
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