Adenovirus E1A blocks oxidant-dependent ferritin induction and sensitizes cells to pro-oxidant cytotoxicity

被引:35
作者
Orino, K
Tsuji, Y
Torti, FM
Torti, SV [1 ]
机构
[1] Wake Forest Univ, Sch Med, Dept Biochem, Winston Salem, NC 27157 USA
[2] Wake Forest Univ, Sch Med, Ctr Comprehens Canc, Winston Salem, NC 27157 USA
[3] Wake Forest Univ, Sch Med, Dept Canc Biol, Winston Salem, NC 27157 USA
[4] Wake Forest Univ, Sch Med, Dept Med, Winston Salem, NC 27157 USA
来源
FEBS LETTERS | 1999年 / 461卷 / 03期
关键词
ferritin; oxidative stress; adenovirus E1A;
D O I
10.1016/S0014-5793(99)01443-X
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
Ferritin is a protein that oxidizes and sequesters intracellular iron in a mineral core. We have reported that the E1A oncogene selectively represses ferritin H transcription, resulting in reduced levels of the ferritin H protein. Here we demonstrate that cells respond to pro-oxidant challenge by inducing ferritin mRNA and protein, and that this response is completely blocked by E1A, Concordantly, E1A sensitized cells to the cytotoxic effects of oxidative stress and enhanced the accumulation of reactive oxygen species in response to prooxidant challenge. These results demonstrate that expression of E1A impedes the cellular response to oxidative stress, including the induction of ferritin. (C) 1999 Federation of European Biochemical Societies.
引用
收藏
页码:334 / 338
页数:5
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