Literature DB >> 2868790

Use of slow Ca2+ channel blockers to enhance inhibition by taxol of growth of drug-sensitive and -resistant Chinese hamster ovary cells.

E Racker, L T Wu, D Westcott.   

Abstract

The toxicity of taxol for drug-sensitive and -resistant Chinese hamster ovary cells has been examined in tissue cultures in the presence and absence of drugs that are being used as slow Ca2+ channel blockers. Enhancement of toxicity was found to be greater in the case of taxol than of daunorubicin. Several blockers including pimozide and nimodipine were more effective as toxicity enhancers than verapamil. Studies of uptake of 14C-labeled daunorubicin revealed a poor correlation between the effectiveness of various drugs to enhance intracellular daunorubicin concentration and their toxicity to cells grown in tissue cultures.

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Year:  1986        PMID: 2868790

Source DB:  PubMed          Journal:  Cancer Treat Rep        ISSN: 0361-5960


  2 in total

1.  Inactivation of L-type Ca channels in embryonic chick ventricle cells: dependence on the cytoskeletal agents colchicine and taxol.

Authors:  A Galli; L J DeFelice
Journal:  Biophys J       Date:  1994-12       Impact factor: 4.033

2.  Correction of altered plasma membrane potentials. A possible mechanism of cyclosporin A and verapamil reversal of pleiotropic drug resistance in neoplasia.

Authors:  B Vayuvegula; L Slater; J Meador; S Gupta
Journal:  Cancer Chemother Pharmacol       Date:  1988       Impact factor: 3.333

  2 in total

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