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Self-regulatory role of 4-hydroxynonenal in signaling for stress-induced programmed cell death

期刊

FREE RADICAL BIOLOGY AND MEDICINE
卷 45, 期 2, 页码 111-118

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.freeradbiomed.2008.04.007

关键词

4-hydroxynonenal; apoptosis; cell cycle signalling; Fas; p53; heat shock factor 1; Daxx

资金

  1. NCI NIH HHS [R01 CA104661, R01 CA077495, CA104661, R01 CA104661-06, CA 77495, R01 CA077495-10] Funding Source: Medline
  2. NEI NIH HHS [R01 EY004396, EY 04396] Funding Source: Medline
  3. NIEHS NIH HHS [ES 012171, R01 ES012171] Funding Source: Medline

向作者/读者索取更多资源

Within the last two decades, 4-hydroxynonenal has emerged as an important second messenger involved in the regulation of various cellular processes. Our recent studies suggest that HNE can induce apoptosis in various cells through the death receptor Fas (CD95)-mediated extrinsic pathway as well as through the p53-dependent intrinsic pathway. Interestingly, through its interaction with the nuclear protein Daxx, HNE can self-limit its apoptotic role by translocating Daxx to cytoplasm where it binds to Fas and inhibits Fas mediated apoptosis. In this paper, after briefly describing recent studies on various biological activities of HNE, based on its interactions with Fas, Daxx, and p53, we speculate on possible mechanisms through which HNE may affect a multitude of cellular processes and draw a parallel between signaling roles of H2O2 and HNE. (C) 2008 Elsevier Inc. All rights reserved.

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