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Cytotoxicity of ketoconazole in malignant cell lines
Authors:C F Rochlitz  L E Damon  M B Russi  A Geddes  E C Cadman
Institution:(1) Cancer Research Institute, 1282-M, University of California San Francisco, 94143 San Francisco, CA, USA;(2) Yale School of Medicine, 333, Cedar Street, P.O. Box 3333, 06510 New Haven, CT, USA
Abstract:Summary The cytotoxic effects of ketoconazole, an antifungal agent known to have some activity against human prostate cancer, adrenal cancer, and male metastatic breast cancer, were evaluated using colony-growth and clonogenic assays in eight malignant cell lines. The cytotoxicity of ketoconazole showed a dose-and time-dependent pattern, with the following concentrations, inhibiting 90% of the growing colonies (IC90): MCF 7 (human breast cancer) 7.25 mgrg/ml, T 47 D (human breast cancer) 9.0 mgrg/ml, MiaPaCa (human pancreatic carcinoma) 10.0 mgrg/ml, COLO 357 (human pancreatic carcinoma) 9.5 mgrg/ml, HCT 8 (human colonic adenocarcinoma) 27.1 mgrg/ml, DU 145 (human prostatic cancer) 40.0 mgrg/ml, AR 42 J (rat pancreatic carcinoma) 9.0 mgrg/ml, and L1210 (murine leukemia) 8.6 mgrg/ml. Since a concentration of 10 mgrg/ml can be achieved in humans, the use of ketoconazole in human malignancies might be worthy of clinical evaluation.This investigation was supported in part by a grant from the German Volkswagen Foundation, Hannover, Federal Republic of Germany and by a gift from Dr Virgil Gianelli, Stockton, California
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