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High resistance to cisplatin in human ovarian cancer cell lines is associated with marked increase of glutathione synthesis
- Source :
- Proceedings of the National Academy of Sciences of the United States of America. 89(7)
- Publication Year :
- 1992
-
Abstract
- Exposure of human ovarian tumor cell lines to cisplatin led to development of cell lines that exhibited increasing degrees of drug resistance, which were closely correlated with increase of the levels of cellular glutathione. Cell lines were obtained that showed 30- to 1000-fold increases in resistance; these cells also had strikingly increased (13- to 50-fold) levels of glutathione as compared with the drug-sensitive cells of origin. These levels of resistance to cisplatin and the cellular glutathione levels are substantially greater than previously reported. Very high cisplatin resistance was associated with enhanced expression of mRNAs for gamma-glutamylcysteine synthetase and gamma-glutamyl transpeptidase; immunoblots showed increase of gamma-glutamylcysteine synthetase but not of glutathione synthetase. Glutathione S-transferase activity was unaffected, as determined with chlorodinitrobenzene as a substrate. These studies suggest the potential value of examining regulation of glutathione synthesis as an indicator of clinical prognosis. The highly resistant cell lines are proving useful for studying the multiple mechanisms by which tumor cells acquire drug- and radiation-resistance.
- Subjects :
- Glutamate-Cysteine Ligase
Drug Resistance
Gene Expression
Drug resistance
Biology
In Vitro Techniques
Ovarian tumor
chemistry.chemical_compound
Gene expression
medicine
Tumor Cells, Cultured
Humans
RNA, Messenger
Glutathione Transferase
Cisplatin
Ovarian Neoplasms
Multidisciplinary
Glutathione
medicine.disease
Molecular biology
Glutathione synthetase
chemistry
Biochemistry
Cell culture
Female
Ovarian cancer
medicine.drug
Research Article
Subjects
Details
- ISSN :
- 00278424
- Volume :
- 89
- Issue :
- 7
- Database :
- OpenAIRE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Accession number :
- edsair.doi.dedup.....226f760b32eee57e49369df8497d30cf