Wan X S, St Clair D K
Graduate Center for Toxicology, University of Kentucky, Lexington 40506-0054.
Cancer Chemother Pharmacol. 1993;33(3):210-4. doi: 10.1007/BF00686218.
Glutathione (GSH) depletion has been studied extensively as a possible means to sensitive tumor cells to radiation treatment and chemotherapy. The present study was undertaken to compare the cytotoxicity of GSH depletion in normal and transformed cells. The results showed that specific inhibition of GSH synthesis by L-buthionine sulfoximine (BSO) caused significantly higher cytotoxicity in "normal" human-lung fibroblast cells than in their transformed counterparts. This finding suggests a possibility that depletion of GSH could be more harmful to normal cells than to transformed and/or tumor cells and that the selective cytotoxicity of BSO to normal cells could limit its potential as an effective sensitizer for cancer treatment.
谷胱甘肽(GSH)耗竭作为一种使肿瘤细胞对放射治疗和化疗敏感的可能手段已得到广泛研究。本研究旨在比较GSH耗竭在正常细胞和转化细胞中的细胞毒性。结果表明,L-丁硫氨酸亚砜胺(BSO)对GSH合成的特异性抑制在“正常”人肺成纤维细胞中引起的细胞毒性显著高于其转化后的对应细胞。这一发现表明,GSH耗竭对正常细胞可能比对转化细胞和/或肿瘤细胞更具危害性,并且BSO对正常细胞的选择性细胞毒性可能会限制其作为癌症治疗有效增敏剂的潜力。