| Literature DB >> 21479360 |
Hiroki Iwata1, Hiromi Sato, Rina Suzuki, Ryota Yamada, Saki Ichinomiya, Midori Yanagihara, Hiroyuki Okabe, Yuko Sekine, Tomohiro Yano, Koichi Ueno.
Abstract
Renal cell carcinoma (RCC) is resistant to chemo-therapy partly due to the overexpression of the P-glycoprotein. Several tumor suppressor genes have been reported to be silenced by hypermethylation of the promoter region in RCC. We recently reported that the in vitro cytotoxicity of vinblastine (VBL) was enhanced by pre-treatment with the demethylating agent, 5-aza-2'-deoxycytidine (Aza), in the RCC cell line, Caki-1. In this study, we investigated the combined effect of Aza and VBL in a Caki-1 xenograft model and in other RCC cell lines in vitro. In the xenograft model, tumor volume and weight were significantly suppressed in the co-treatment group, compared to the control, and the expressions of P-glycoprotein, Bcl-2 and cyclin B1 were reduced. Thus, this combined effect could be mediated by the accumulation of intracellular VBL and the enhancement of apoptosis and cell cycle arrest. More-over, the cytotoxicity of VBL was enhanced in vitro in three RCC cell lines by Aza treatment. These findings suggest that the combination treatment with Aza and VBL is effective against RCC.Entities:
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Year: 2011 PMID： 21479360 DOI： 10.3892/ijo.2011.999
Source DB: PubMed Journal: Int J Oncol ISSN： 1019-6439 Impact factor: 5.650