EFFECT OF GLUTATHIONE DEPLETION ON THE CYTOTOXICITY OF CISPLATIN AND IPROPLATIN IN A HUMAN-MELANOMA CELL-LINE

Citation
L. Pendyala et al., EFFECT OF GLUTATHIONE DEPLETION ON THE CYTOTOXICITY OF CISPLATIN AND IPROPLATIN IN A HUMAN-MELANOMA CELL-LINE, Cancer chemotherapy and pharmacology, 40(1), 1997, pp. 38-44
Citations number
39
Categorie Soggetti
Pharmacology & Pharmacy",Oncology
ISSN journal
03445704
Volume
40
Issue
1
Year of publication
1997
Pages
38 - 44
Database
ISI
SICI code
0344-5704(1997)40:1<38:EOGDOT>2.0.ZU;2-H
Abstract
Previous studies from our laboratory have indicated that glutathione ( GSH) may affect the cytotoxicity of iproplatin to a greater extent tha n four other platinum agents tested including cisplatin. Therefore we studied the effect of GSH depletion by buthionine sulfoximine (BSO) on the cytotoxicity of iproplatin and cisplatin in a human melanoma cell line SK-MEL-2. Depletion of GSH was dependent on the concentration an d time of incubation with BSO. BSO (100 mu M) depleted GSH by 85% at 2 4 h and by 91% at 48 h. BSO (10 to 100 mu M) by itself was not cytotox ic to SK-MEL-2 cells. At 85% depletion of GSH, cytotoxicity of ipropla tin was increased by a factor of >7 and that of cisplatin by <2. These results confirm the previous finding that GSH interferes with the cyt otoxicity of iproplatin to a significantly greater extent than that of cisplatin. Equitoxic IC65 and IC90 values of cisplatin (2 mu M and 5 mu M) or iproplatin (25 mu M and 50 mu M) had no effect on the intrace llular GSH levels in SK-MEL-2 cells. Also, depletion of GSH by BSO had no effect on the accumulation of platinum from either cisplatin or ip roplatin in this cell line. Our results suggest that the effect of GSH on the cytotoxicity of cisplatin and iproplatin in this cell line was not a consequence either of differences in GSH-Pt conjugate formation , or of differences in platinum accumulation induced by GSH depletion. GSH may have modulated the cytotoxicity of these platinum complexes b y other means such as effects on DNA repair, apoptosis, free radical s cavenging or through other yet unidentified mechanisms.