POSITIVE CORRELATION BETWEEN CELLULAR GLUTATHIONE AND ACQUIRED CISPLATIN RESISTANCE IN HUMAN OVARIAN-CANCER CELLS

While multiple changes are frequently found to be associated with cisplatin resistance in a variety of tumor cell lines, a cause-effect relationship of these alterations with the resistant phenotype has not been established. In order to identity the resistance-relevant determinants, a series of cisplatin-resistant sublines with different degrees of resistance to cisplatin was developed in a human ovarian carcinoma cell line (0-129). Three derived resistant cell lines displayed 2.1-fold (0-129/DDP4, low), 4.1-fold (0-129/DDP8, moderate) and 6.3-fold (0-129/DDP16, high) resistance, respectively, to cisplatin, compared with the sensitive parental line 0-129. While the activity of poly(ADP-ribose) polymerase, an enzyme proposed to be involved in DNA repair, was elevated in all three resistant lines, a significant karyotypic change was observed only in the high-resistance line with the karyotype alteration from near diploidy to heteroploidy. The moderate (4.1-fold) and high (6.3-fold) DDP resistance was associated with a slow proliferation rate in drug-free medium, but cellular glutathione level was highly correlated with DDP sensitivity in all four cell lines. Taken together, the present studies establish that while many changes at cellular level can occur with development of cisplatin resistance, only elevation of intracellular glutathione concentration appears to be related to the resistance phenotype in these human ovarian cancer cells.