In order to study the mechanism of the resistance to chemotherapeutic agents, especially ACNU [1-(4-amino-2-methyl-5-pyrimidinyl) methyl-3-(2-chloroethyl)-3-nitrosourea hydrochloride), two variant cell lines (C6/ACNU and 9L/ACNU) resistant to ACNU were selected in vivo from rat C6 and 9L glioma, res
Glutathione and cellular response of ACNU-resistant rat glioma sublines to drugs and radiation
โ Scribed by Yuji Saito; Takuhiro Hotta; Takasi Mikami; Kaoru Kurisu; Kenji Yamada; Katuzou Kiya; Keiichi Kawamoto; Tohru Uozumi; Yosihiro Nakada
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- French
- Weight
- 543 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
โฆ Synopsis
Three ACNU-resistant sublines (Ri, R, and Rid. from rat glioma 9L cells showed cross-resistance to vinblastine, adriamycin, and VP-16. Among these, the R, subline also acquired radioresistance under aerobic conditions. Total glutathione levels in these sublines were elevated 2-to 3-fold. Treatment of the cells with BSO, a specific inhibitor of GSH synthesis, resulted in decreased intracellular total glutathione levels in all 4 cell lines to about 10% of control levels. However, sensitivity to radiation or to chemicals did not change accordingly. Treatment of 9L cells with OTZ, a precursor of cysteine, resulted in a rise in intracellular GSH levels but it did not correlate with sensitivity to X-ray or to ACNU. These results suggest that, in terms of cellular sensitivity to radiation or ACNU, total glutathione level alone cannot serve as a predictive indicator.
๐ SIMILAR VOLUMES
Human glioma cells were exposed to stepwise increasing concentrations of cisplatin and given a final, acute, high concentration treatment of cisplatin. From the surviving cells, eight cisplatin resistant clones were selected. These clones demonstrated a range of cisplatin sensitivities that were ret
Three groups of rats were given avoidance training followed by extinction. One group received one acquisition session immediately followed by extinction. A second group received two acquisition sessions while in the non-drug state, followed by extinction. A third group received two acquisition sessi