Phosphoinositide 3-kinase signaling in the cellular response to oxidative stress

被引:72
作者
Barthel, A
Klotz, LO [1 ]
机构
[1] Univ Dusseldorf, Inst Biochem & Mol Biol 1, D-40225 Dusseldorf, Germany
[2] Univ Dusseldorf, Abt Endokrinol Diabetol & Rheumatol, D-40225 Dusseldorf, Germany
关键词
Akt; FoxO-proteins; oxidant signaling; oxidative stress; phosphoinositide 3 '-kinase (PI 3-kinase); protein kinase B; signal transduction;
D O I
10.1515/BC.2005.026
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
Oxidative stress is linked to the pathogenesis and pathobiochemistry of various diseases, including cancer, diabetes and cardiovascular disorders. The non-specific damaging effect of reactive oxygen species (ROS) generated during oxidative stress is involved in the development of diseases, as well as the activation of specific signaling cascades in cells exposed to the higher oxidant load. A cellular signaling cascade that is activated by several types of reactive oxygen species is the phosphoinositide 3'-kinase (PI 3-kinase)/protein kinase B (PKB) pathway, which regulates cellular survival and fuel metabolism, thus establishing a link between oxidative stress and signaling in neoplastic, metabolic or degenerative diseases. Several links of PI 3-kinase/PKB signaling to ROS are discussed in this review, with particular focus on the molecular mechanisms involved in the regulation of PI 3-kinase signaling by oxidative stress and important players such as (i) the glutathione and glutaredoxin system, (ii) the thioredoxin system and (iii) Ser/ Thr- and Tyr phosphatases.
引用
收藏
页码:207 / 216
页数:10
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