Giuliano Michela, Pellerito Ornella, Portanova Patrizia, Calvaruso Giuseppe, Santulli Andrea, De Blasio Anna, Vento Renza, Tesoriere Giovanni
Dipartimento di Scienze Biochimiche, Università di Palermo, Via del Vespro 129, 90127 Palermo, Italy.
Biochimie. 2009 Apr;91(4):457-65. doi: 10.1016/j.biochi.2008.11.003. Epub 2008 Nov 27.
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 PPARgamma in a dose- and time-dependent manner. The addition of the PPARgamma 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 PPARgamma plays a key role in WIN-induced apoptosis. Altogether, the results seem to indicate a potential therapeutic role of WIN in hepatic cancer treatment.
最近研究表明,大麻素可诱导不同肿瘤细胞系的生长抑制和凋亡。在本研究中,我们研究了合成强效大麻素受体激动剂WIN 55,212-2(WIN)对肝癌HepG2细胞的影响,并提出了可能的信号转导途径。在这些细胞中,WIN诱导明显的凋亡效应,同时死亡信号因子Bax、Bcl-X(S)、t-Bid上调,存活因子survivin、磷酸化AKT、Hsp72和Bcl-2下调。此外,WIN诱导的凋亡与细胞荧光分析显示的JNK/p38 MAPK途径激活和线粒体去极化有关。结果还表明,在HepG2细胞中,WIN以剂量和时间依赖性方式显著增加转录因子PPARγ的水平。添加PPARγ拮抗剂GW9662和T0070907可显著降低药物对细胞活力以及survivin、磷酸化AKT和磷酸化BAD水平的影响,表明PPARγ在WIN诱导的凋亡中起关键作用。总之,这些结果似乎表明WIN在肝癌治疗中具有潜在的治疗作用。