Apoptosis induced in HepG2 cells by the synthetic cannabinoid WIN: Involvement of the transcription factor PPARγ

被引:60
作者
Giuliano, Michela [1 ]
Pellerito, Ornella [1 ]
Portanova, Patrizia [1 ]
Calvaruso, Giuseppe [1 ]
Santulli, Andrea [1 ]
De Blasio, Anna [1 ]
Vento, Renza [1 ]
Tesoriere, Giovanni [1 ]
机构
[1] Univ Palermo, Dipartimento Sci Biochim, I-90127 Palermo, Italy
关键词
Cannabinoids; PPAR gamma; Apoptosis; Hepatoma cells; ACTIVATED-RECEPTOR-GAMMA; CANCER-CELLS; CERAMIDE ACCUMULATION; PROSTATE-CANCER; CYCLE ARREST; LIPID RAFTS; CASCADE; SYSTEM; WIN55,212-2; BORTEZOMIB;
D O I
10.1016/j.biochi.2008.11.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
It has recently been shown that cannabinoids induce growth inhibition and apoptosis in different tumour cell lines. In the current study, the effects of WIN 55,212-2 (WIN), a synthetic and potent cannabinoid receptor agonist, are investigated in hepatoma HepG2 cells and a possible signal transduction pathway is proposed. In these cells, WIN induces a clear apoptotic effect which was accompanied by up-regulation of the death-signalling factors Bax, Bcl-X-S, t-Bid and down-regulation of the survival factors survivin, phospho-AKT, Hsp72 and Bcl-2. Moreover, WIN-induced apoptosis is associated with JNK/p38 MAPK pathway activation and mitochondrial depolarisation demonstrated by a cytofluorimetric assay. The results also show that in HepG2 cells WIN markedly increases the level of the transcription factor PPAR gamma in a dose- and time-dependent manner. The addition of the PPAR gamma antagonists GW9662 and T0070907 significantly reduces the effects of the drug on both cell viability and the levels of survivin, phospho-AKT and phospho-BAD, suggesting that PPAR gamma plays a key role in WIN-induced apoptosis. Altogether, the results seem to indicate a potential therapeutic role of WIN in hepatic cancer treatment. (C) 2008 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:457 / 465
页数:9
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