Glutathione in metastases: From mechanisms to clinical applications

被引:47
作者
Estrela, Jose M. [1 ,2 ]
Ortega, Angel [2 ]
Mena, Salvador [2 ]
Antoni Sirerol, J. [2 ]
Obrador, Elena [1 ]
机构
[1] Univ Valencia, Fac Med & Odontol, Dept Physiol, 15 Av Blasco Ibanez, Valencia 46010, Spain
[2] Univ Valencia, Fac Pharm, Dept Physiol, Valencia, Spain
关键词
Glutathione; cancer; metastases; stress; neuroendocrine regulation; oncotherapy; B16; MELANOMA-CELLS; CANCER STEM-CELLS; PROTEIN S-GLUTATHIONYLATION; ENDOTHELIAL GROWTH-FACTOR; OXIDATIVE STRESS; NITRIC-OXIDE; MULTIDRUG-RESISTANCE; HYDROGEN-PEROXIDE; TUMOR-SUPPRESSOR; REDOX REGULATION;
D O I
10.3109/10408363.2015.1136259
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Metastatic spread, not primary tumors, is the leading cause of cancer death. Glutathione (-glutamyl-cysteinyl-glycine, GSH) is particularly relevant in cancer cells as it is involved in regulating carcinogenic mechanisms, growth and dissemination, and multidrug and radiation resistance. Upon interaction of metastatic cells with the vascular endothelium, a high percentage of metastatic cells with high GSH levels survive the combined nitrosative and oxidative stresses elicited by the vascular endothelium. GSH release from different organs, mainly the liver, and its interorgan transport through the blood circulation to metastatic foci, promote their growth. This review focuses on the relationship among GSH and different key mechanisms that facilitate metastatic cell survival and growth, i.e. adaptive responses to stress, cell death evasion and utilization of physiological neuroendocrine mechanisms. Different strategies that are aimed at sensitizing metastases to cancer therapy by depleting metastatic cell GSH are analyzed.
引用
收藏
页码:253 / 267
页数:15
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