Emerging Regulatory Paradigms in Glutathione Metabolism

被引:126
|
作者
Liu, Yilin [1 ,2 ]
Hyde, Annastasia S. [1 ,2 ]
Simpson, Melanie A. [1 ,2 ]
Barycki, Joseph J. [1 ,2 ]
机构
[1] Univ Nebraska, Dept Biochem, Lincoln, NE 68583 USA
[2] Univ Nebraska, Redox Biol Ctr, Lincoln, NE 68583 USA
来源
REDOX AND CANCER, PT A | 2014年 / 122卷
关键词
GAMMA-GLUTAMYL-TRANSPEPTIDASE; LIGASE CATALYTIC SUBUNIT; 5-L-OXOPROLINE PYROGLUTAMIC ACID; CYSTEINE LIGASE; HELICOBACTER-PYLORI; URINARY-EXCRETION; MODIFIER SUBUNIT; MESSENGER-RNA; CANCER-CELLS; CRYSTAL-STRUCTURE;
D O I
10.1016/B978-0-12-420117-0.00002-5
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
One of the hallmarks of cancer is the ability to generate and withstand unusual levels of oxidative stress. In part, this property of tumor cells is conferred by elevation of the cellular redox buffer glutathione. Though enzymes of the glutathione synthesis and salvage pathways have been characterized for several decades, we still lack a comprehensive understanding of their independent and coordinate regulatory mechanisms. Recent studies have further revealed that overall central metabolic pathways are frequently altered in various tumor types, resulting in significant increases in biosynthetic capacity and feeding into glutathione synthesis. In this review, we will discuss the enzymes and pathways affecting glutathione flux in cancer and summarize current models for regulating cellular glutathione through both de novo synthesis and efficient salvage. In addition, we examine the integration of glutathione metabolism with other altered fates of intermediary metabolites and highlight remaining questions about molecular details of the accepted regulatory modes.
引用
收藏
页码:69 / 101
页数:33
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