Cancer Chemotherapy and Pharmacology

, Volume 40, Issue 1, pp 38–44

Effect of glutathione depletion on the cytotoxicity of cisplatin and iproplatin in a human melanoma cell line

Authors

  • L. Pendyala
    • Department of Investigational Therapeutics, Division of Medicine, Roswell Park Cancer Institute, Buffalo, NY 14263, USA Tel. 716-845-3287; Fax 716-845-8008
  • R. Perez
    • Department of Investigational Therapeutics, Division of Medicine, Roswell Park Cancer Institute, Buffalo, NY 14263, USA Tel. 716-845-3287; Fax 716-845-8008
  • A. Weinstein
    • Department of Investigational Therapeutics, Division of Medicine, Roswell Park Cancer Institute, Buffalo, NY 14263, USA Tel. 716-845-3287; Fax 716-845-8008
  • J. Zdanowicz
    • Department of Investigational Therapeutics, Division of Medicine, Roswell Park Cancer Institute, Buffalo, NY 14263, USA Tel. 716-845-3287; Fax 716-845-8008
  • P. J. Creaven
    • Department of Investigational Therapeutics, Division of Medicine, Roswell Park Cancer Institute, Buffalo, NY 14263, USA Tel. 716-845-3287; Fax 716-845-8008
ORIGINAL ARTICLE

DOI: 10.1007/s002800050622

Cite this article as:
Pendyala, L., Perez, R., Weinstein, A. et al. Cancer Chemother Pharmacol (1997) 40: 38. doi:10.1007/s002800050622

Abstract

 Previous studies from our laboratory have indicated that glutathione (GSH) may affect the cytotoxicity of iproplatin to a greater extent than 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 and time of incubation with BSO. BSO (100 μM) depleted GSH by 85% at 24 h and by 91% at 48 h. BSO (10 to 100 μM) by itself was not cytotoxic to SK-MEL-2 cells. At 85% depletion of GSH, cytotoxicity of iproplatin was increased by a factor of >7 and that of cisplatin by <2. These results confirm the previous finding that GSH interferes with the cytotoxicity of iproplatin to a significantly greater extent than that of cisplatin. Equitoxic IC65 and IC90 values of cisplatin (2 μM and 5 μM) or iproplatin (25 μM and 50 μM) had no effect on the intracellular 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 iproplatin 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 by other means such as effects on DNA repair, apoptosis, free radical scavenging or through other yet unidentified mechanisms.

Key words Glutathione Cytotoxicity Cisplatin Iproplatin

Copyright information

© Springer-Verlag Berlin Heidelberg 1997