Disruption of the DT diaphorase (NQ01) gene in mice leads to increased menadione toxicity

被引:221
作者
Radjendirane, V
Joseph, P
Lee, YH
Kimura, S
Klein-Szanto, AJP
Gonzalez, FJ
Jaiswal, AK
机构
[1] Baylor Coll Med, Dept Pharmacol, Houston, TX 77030 USA
[2] NCI, Lab Metab, NIH, Bethesda, MD 20892 USA
[3] Fox Chase Canc Ctr, Dept Pathol, Philadelphia, PA 19111 USA
关键词
D O I
10.1074/jbc.273.13.7382
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
NAD(P)H:quinone oxidoreductase 1 (NQO1) is a flavoenzyme that catalyzes two-electron reductive metabolism and detoxification of quinones and their derivatives leading to protection of cells against redox cycling and oxidative stress. To examine the in vivo role of NQO1, a NQO1-null mouse was produced using targeted gene disruption. Mice lacking NQO1 gene expression showed no detectable phenotype and were indistinguishable from wild-type mice. However, NQO1-null mice exhibited increased toxicity when administered menadione compared with wild-type mice. These results establish a role for NQO1 in protection against quinone toxicity. The NQO1-null mice are a model for NQO1 deficiency in humans and can be used to determine the role of this enzyme in sensitivity to toxicity and carcinogenesis.
引用
收藏
页码:7382 / 7389
页数:8
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