Skov K A, Korbelik M, Palcic B, Skarsgard L D
Int J Radiat Oncol Biol Phys. 1982 Mar-Apr;8(3-4):697-700. doi: 10.1016/0360-3016(82)90715-5.
Cell inactivation and DNA damage (single-strand breaks) were used to study the effects of inhibitors of anaerobic glucose oxidation on the toxicity of misonidazole to hypoxic Chinese hamster cells. Citrate and 2-deoxyglucose produced no effects on the toxicity. 5-thio-D-glucose (5-TG) protected cells of the CH2B2 line to some extent (SSB decreased by about 30%). In the CHO lines used (wild, and ethylmethanesulfonate-sensitive mutants), 5-TG had varied effects. Non-protein sulfhydryl (NPSH) levels were measured in all lines. Cells with lower NPSH levels are more sensitive to misonidazole; these are the cells which are protected by 5-TG. Cell line variations must be considered when studying interactions between a drug and other forms of treatment as possible treatments of cancer.
利用细胞失活和DNA损伤(单链断裂)来研究厌氧葡萄糖氧化抑制剂对米索硝唑对缺氧中国仓鼠细胞毒性的影响。柠檬酸盐和2-脱氧葡萄糖对毒性没有影响。5-硫代-D-葡萄糖(5-TG)在一定程度上保护了CH2B2细胞系(单链断裂减少约30%)。在所使用的CHO细胞系(野生型和对乙基甲磺酸敏感的突变体)中,5-TG产生了不同的影响。测量了所有细胞系中的非蛋白质巯基(NPSH)水平。NPSH水平较低的细胞对米索硝唑更敏感;这些细胞正是受到5-TG保护的细胞。在研究药物与其他治疗形式之间的相互作用作为癌症可能的治疗方法时,必须考虑细胞系的差异。