| Literature DB >> 19375851 |
Sharad S Singhal1, Sushma Yadav, Rit Vatsyayan, Pankaj Chaudhary, Jozef Borvak, Jyotsana Singhal, Sanjay Awasthi.
Abstract
RLIP76 is a stress-responsive <span class="Chemical">glutathione-electrophile-conjugates (GS-E) and drugs transporter which is over-expressed in different types of cancers. Cdc2 is a cell-cycle check point control kinase which has been shown to bind to RLIP76 during mitosis, such that endocytosis is inhibited. In present studies, we have purified cdc2 and examined its effect on the transport activity of RLIP76 reconstituted into artificial liposomes. Both doxorubicin (DOX) and dinitro-phenyl S-glutathione (DNP-SG) transport were inhibited by cdc2 in a concentration dependent manner. Liposomal delivery of cdc2 to H358 cells caused apoptosis, resulted in an increased intracellular doxorubicin-accumulation and decreased rate of efflux from the cells. In the present communication, we propose that the accumulation-deficient drug-resistance mediated by RLIP76 can be modulated by inhibition of RLIP76 transport activity by cdc2.Entities:
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Year: 2009 PMID： 19375851 PMCID： PMC2721022 DOI： 10.1016/j.canlet.2009.03.033
Source DB: PubMed Journal: Cancer Lett ISSN： 0304-3835 Impact factor: 8.679