HIV protease inhibitor nelfinavir inhibits growth of human melanoma cells by induction of cell cycle arrest

被引:70
作者
Jiang, Wei
Mikochik, Peter J.
Ra, Jin H.
Lei, Hanqin
Flaherty, Keith T.
Winkler, Jeffrey D.
Spitz, Francis R.
机构
[1] Univ Penn, Med Ctr, Dept Surg, Div Endocrine & Oncol Surg, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Chem, Philadelphia, PA 19104 USA
[3] Univ Penn, Abramson Canc Ctr, Philadelphia, PA 19104 USA
关键词
D O I
10.1158/0008-5472.CAN-06-3377
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
HIV protease inhibitors (HIV PI) are a class of antiretroviral drugs that are designed to target the viral protease. Unexpectedly, this class of drugs is also reported to have antitumor activity. In this study, we have evaluated the in vitro activity of nelfinavir, a HIV PI, against human melanoma cells. Nelfinavir inhibits the growth of melanoma cell lines at low micromolar concentrations that are clinically attainable. Nelfinavir promotes apoptosis and arrests cell cycle at G(1) phase. Cell cycle arrest is attributed to inhibition of cyclin-dependent kinase 2 (CDK2) and concomitant dephosphorylation of retinoblastoma tumor suppressor. We further show that nelfinavir inhibits CDK2 through proteasome-dependent degradation of Cdc25A phosphatase. Our results suggest that nelfinavir is a promising candidate chemotherapeutic agent for advanced melanoma, for which novel and effective therapies aloe urgently needed.
引用
收藏
页码:1221 / 1227
页数:7
相关论文
共 22 条
[1]   Pharmacokinetics, food intake requirements and tolerability of once-daily combinations of nelfinavir and low-dose ritonavir in healthy volunteers [J].
Aarnoutse, RE ;
Droste, JAH ;
van Oosterhout, JJG ;
Koopmans, PP ;
Popescu, M ;
Reiss, P ;
Hekster, YA ;
Burger, DM .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2003, 55 (02) :115-125
[2]   An inhibitor of HIV-1 protease modulates proteasome activity, antigen presentation, and T cell responses [J].
André, P ;
Groettrup, M ;
Klenerman, P ;
de Giuli, R ;
Booth, BL ;
Cerundolo, V ;
Bonneville, M ;
Jotereau, F ;
Zinkernagel, RM ;
Lotteau, V .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (22) :13120-13124
[3]   Identification of arctigenin as an antitumor agent having the ability to eliminate the tolerance of cancer cells to nutrient starvation [J].
Awale, S ;
Lu, J ;
Kalauni, SK ;
Kurashima, Y ;
Tezuka, Y ;
Kadota, S ;
Esumi, H .
CANCER RESEARCH, 2006, 66 (03) :1751-1757
[4]   Degradation of Cdc25A by β-TrCP during S phase and in response to DNA damage [J].
Busino, L ;
Donzelli, M ;
Chiesa, M ;
Guardavaccaro, D ;
Ganoth, D ;
Dorrello, NV ;
Hershko, A ;
Pagano, M ;
Draetta, GF .
NATURE, 2003, 426 (6962) :87-91
[5]   Dual mode of degradation of Cdc25 A phosphatase [J].
Donzelli, M ;
Squatrito, M ;
Ganoth, D ;
Hershko, A ;
Pagano, M ;
Draetta, GF .
EMBO JOURNAL, 2002, 21 (18) :4875-4884
[6]  
Gaedicke S, 2002, CANCER RES, V62, P6901
[7]   HIV protease inhibitors block Akt signaling and radiosensitize tumor cells both in vitro and in vivo [J].
Gupta, AK ;
Cerniglia, GJ ;
Mick, R ;
McKenna, WG ;
Muschel, RJ .
CANCER RESEARCH, 2005, 65 (18) :8256-8265
[8]  
Ikezoe T, 2004, MOL CANCER THER, V3, P473
[9]  
Ikezoe T, 2000, BLOOD, V96, P3553
[10]   HIV-1 protease inhibitor, ritonavir:: A potent inhibitor of CYP3A4, enhanced the anticancer effects of docetaxel in androgen-independent prostate cancer cells in vitro and in vivo [J].
Ikezoe, T ;
Hisatake, Y ;
Takeuchi, T ;
Ohtsuki, Y ;
Yang, Y ;
Said, JW ;
Taguchi, H ;
Koeffler, HP .
CANCER RESEARCH, 2004, 64 (20) :7426-7431