Glutathione metabolism in cancer progression and treatment resistance

被引:876
|
作者
Bansal, Ankita [1 ]
Simon, M. Celeste [1 ,2 ]
机构
[1] Univ Penn, Perelman Sch Med, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
[2] Univ Penn, Perelman Sch Med, Dept Cell & Dev Biol, Philadelphia, PA 19104 USA
来源
JOURNAL OF CELL BIOLOGY | 2018年 / 217卷 / 07期
基金
美国国家卫生研究院;
关键词
GAMMA-GLUTAMYL-TRANSPEPTIDASE; TRANSCRIPTION FACTOR NRF2; CYSTINE/GLUTAMATE ANTIPORTER; OXIDATIVE DAMAGE; LUNG-CANCER; PATHWAY; CELLS; TRANSFERASE; ACTIVATION; INHIBITION;
D O I
10.1083/jcb.201804161
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Glutathione (GSH) is the most abundant antioxidant found in living organisms and has multiple functions, most of which maintain cellular redox homeostasis. GSH preserves sufficient levels of cysteine and detoxifies xenobiotics while also conferring therapeutic resistance to cancer cells. However, GSH metabolism plays both beneficial and pathogenic roles in a variety of malignancies. It is crucial to the removal and detoxification of carcinogens, and alterations in this pathway can have a profound effect on cell survival. Excess GSH promotes tumor progression, where elevated levels correlate with increased metastasis. In this review, we discuss recent studies that focus on deciphering the role of GSH in tumor initiation and progression as well as mechanisms underlying how GSH imparts treatment resistance to growing cancers. Targeting GSH synthesis/utilization therefore represents a potential means of rendering tumor cells more susceptible to different treatment options such as chemotherapy and radiotherapy.
引用
收藏
页码:2291 / 2298
页数:8
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