ISSN:
1432-0843
Schlagwort(e):
Key words Head and neck cancer
;
Glutathione
;
Cisplatin
;
γ-Glutamyl cysteine synthetase
Quelle:
Springer Online Journal Archives 1860-2000
Thema:
Medizin
Notizen:
Abstract Purpose: To correlate cellular glutathione content and γ-glutamyl cysteine synthetase (γGCS) mRNA expression with cisplatin sensitivity in a panel of seven head and neck squamous cancer cell lines. Methods: Cisplatin IC50 was determined for each cell line using a sodium tetreazolium (XTT) assay. Cellular glutathione content was measured by using a previously reported enzymic method. γGCS mRNA expression was measured using an RNase protection assay. Results: Total cellular glutathione was an excellent predictor of cisplatin sensitivity in this series of cell lines. The IC50 for cisplatin in the cell line with the highest glutathione concentration was approximately 90 times higher than in the cell line with the lowest glutathione concentration. Regression analysis showed a highly statistically significant positive correlation between cisplatin IC50 and cellular glutathione (coefficient of determination R 2=0.81, P=0.0012). Somewhat surprisingly, in contrast to previous studies in ovarian cancer, γGCS mRNA expression in these cell lines was not significantly predictive of either total cellular glutathione or cisplatin sensitivity (R 2=0.005, P=0.84). As expected, treatment of resistant cell lines with buthionine sulfoximine resulted in decreased cellular glutathione and enhanced cisplatin sensitivity. Conclusions: Our results suggest that glutathione may be an important determinant of cisplatin sensitivity in clinical head and neck cancer. Since cisplatin is the most active chemotherapy drug for the treatment of this disease, this correlation may have important clinical relevance. The lack of correlation between glutathione level and γGCS expression suggests that salvage or alternate synthetic pathways may be critical in these cells.
Materialart:
Digitale Medien
URL:
http://dx.doi.org/10.1007/s002800050629
Permalink
