细胞毒性
米索硝唑
丁硫胺
谷胱甘肽
放射增敏剂
体外
化学
K562细胞
细胞培养
药理学
生物化学
分子生物学
生物
医学
内科学
酶
遗传学
放射治疗
作者
Yujia Jin,Ling Ding,Zhifa Shen,Renyue Cai,L M Xu,Ji Yang,Xin Jin,Weili Lu,Jie Xu
出处
期刊:PubMed
[National Institutes of Health]
日期:1992-08-01
卷期号:105 (8): 647-50
被引量:1
摘要
An inhibitor of glutathione biosynthesis, buthionine sulphoximine (BSO), was used to deplete the endogenous thiols in mammalian cells in vitro. In this study, the cytotoxicity of BSO and BSO combined with the hypoxic cell radiosensitizer misonidazole (MISO) was investigated. Both aerobic and hypoxic cytotoxicity of MISO was found to be increased. The concentration of BSO required to reduce the colony forming ability to 50% (Cc) for the chronic cytotoxicity on V79 cells was 0.03 mmol/L under aerobic condition, while the Cc for the acute cytotoxicity on V79 cells under hypoxic and aerobic conditions was 0.4 and 0.5 mmol/L. The growth inhibition rate of human tumor cells K562 and SGC-7901 by BSO was 6.89-26.06% and 12.01-55.69%, respectively. Enhanced cytotoxicity activity was observed when BSO was used in combination with cis-dichlorodiamino Pt(II) or 5-fluorouracil.
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