a Department of Physiology , Faculty of Medicine and Odontology and.
b Department of Physiology , Faculty of Pharmacy, University of Valencia , Valencia , Spain.
Crit Rev Clin Lab Sci. 2016 Aug;53(4):253-67. doi: 10.3109/10408363.2015.1136259. Epub 2016 Feb 18.
Metastatic spread, not primary tumors, is the leading cause of cancer death. Glutathione (γ-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.
转移扩散而非原发性肿瘤是癌症死亡的主要原因。谷胱甘肽(γ-谷氨酰半胱氨酸甘氨酸,GSH)在癌细胞中尤为重要,因为它参与调节致癌机制、生长和扩散以及多药和辐射耐药性。当转移细胞与血管内皮相互作用时,高比例的高 GSH 水平的转移细胞能够在血管内皮引发的联合硝化和氧化应激下存活下来。GSH 从不同器官(主要是肝脏)释放,并通过血液循环在器官间运输到转移灶,促进其生长。本综述重点讨论了 GSH 与促进转移细胞存活和生长的不同关键机制之间的关系,即对压力的适应性反应、细胞死亡逃逸以及对生理神经内分泌机制的利用。分析了旨在通过耗尽转移细胞 GSH 使转移对癌症治疗敏感的不同策略。