Quinone oxidoreductases in protection against myelogenous hyperplasia and benzene toxicity

被引:46
作者
Iskander, K [1 ]
Jaiswal, AK [1 ]
机构
[1] Baylor Coll Med, Dept Pharmacol, Houston, TX 77030 USA
关键词
NAD(P)H : quinone oxidoreductase1; NRH : quinone oxidoreductase2; quinones; metabolic detoxification; myeloid hyperplasia and leukemia; chemoprevention;
D O I
10.1016/j.cbi.2005.03.019
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
Quinone oxidoreductases (NQO1 and NQO2) are cytosolic proteins that catalyze metabolic reduction of quinones and its derivatives to protect cells against redox cycling and oxidative stress. In humans, a high percentage of individuals with myeloid and other types of leukemia are homo- and heterozygous for a null mutant allele of NQO1. The NQO2 locus is also highly polymorphic in humans. Recently, we generated NQO1-/- and NQO2-/- mice deficient in NQO1 and NQO2 protein and activity, respectively. These mice showed no detectable developmental abnormalities and were indistinguishable from wild type mice. Interestingly, all the mice lacking expression of NQO1 and NQO2 protein demonstrated myelogenous hyperplasia of the bone marrow and increased granulocytes in the peripheral blood. Decreased apoptosis contributed to myelogenous hyperplasia. The studies on short-term exposure of NQO1-/- mice to benzene demonstrated substantially greater benzene-induced toxicity, as compared to wild type mice. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:147 / 157
页数:11
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