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Title: Depletion of intracellular GSH and NPSH by buthionine sulfoximine and diethyl maleate: factors that influence enhancement of aerobic radiation response

Conference · · Int. J. Radiat. Oncol., Biol. Phys.; (United States)
OSTI ID:6408307

Many investigators have observed aerobic sensitization of V79, CHO and A549 (human lung carcinoma) cells upon depletion of GSH using buthionine sulfoximine (BSO). Recently the authors discovered that this aerobic sensitization can be reversed if WR-2721 or N-acetylcysteine is added to the cells just prior to irradiation. Reversal requires that the exogenous thiols be present during the time of irradiation. One possible explanation was that these thiols entered the cells and either increased the pool of cellular nonprotein thiols or reversed the thiol-depleted state by stimulation of GSH synthesis. Cells treated with BSO do not readily regenerate intracellular GSH because this agent irreversibly inhibits ..gamma..-glutamyl synthetase. They found that addition of WR-2721 or N-acetylcysteine to BSO-treated cells did not affect the rate of regeneration of intracellular GSH. Thus, reversal of the aerobic sensitization of A549 cells by BSO cannot be explained on the basis of intracellular thiol levels alone, or by rapid reversal of BSO inhibition. In addition, diethylmaleate (DEM)-treated cells are considerably different from BSO-treated cells with respect to the ability to regenerate GSH.

Research Organization:
Case Western Reserve Univ., Cleveland, OH
OSTI ID:
6408307
Report Number(s):
CONF-8311204-
Journal Information:
Int. J. Radiat. Oncol., Biol. Phys.; (United States), Vol. 10:8; Conference: Conference on chemical modifiers of cancer treatment, Banff, Alberta, Canada, 27 Nov 1983
Country of Publication:
United States
Language:
English

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