凋亡和自噬的代谢应激反应在肿瘤抑制中的作用。

E White
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引用次数: 32

摘要

代谢应激是促进细胞凋亡介导的肿瘤抑制的重要刺激物。肿瘤代谢应激的产生有多种因素,包括血管生成不足导致的营养供应不足和细胞无限制增殖的高代谢需求。肿瘤细胞的高代谢需求只会因依赖低效率的糖酵解过程而加剧。近年来,肿瘤细胞通过自噬的分解代谢过程在代谢应激中存活下来。自噬还作为一种肿瘤抑制机制,通过防止细胞死亡和炎症,保护基因组免受损伤和遗传不稳定。自噬如何保护基因组尚不清楚,但可能与它在维持代谢或清除受损蛋白质和细胞器以及减轻氧化应激中的作用有关。这些发现阐明了代谢在癌症进展中的重要作用,并为癌症治疗中的代谢调节提供了具体的预测。
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Role of the metabolic stress responses of apoptosis and autophagy in tumor suppression.

Metabolic stress is an important stimulus that promotes apoptosis-mediated tumor suppression. Metabolic stress arises in tumors from multiple factors that include insufficient nutrient supply caused by deficient angiogenesis and high metabolic demand of unrestrained cell proliferation. The high metabolic demand of tumor cells is only exacerbated by reliance on the inefficient process of glycolysis for energy production. Recently it has become clear that tumor cells survive metabolic stress through the catabolic process of autophagy. Autophagy also functions as a tumor suppression mechanism by preventing cell death and inflammation and by protecting the genome from damage and genetic instability. How autophagy protects the genome is not yet clear but may be related to its roles in sustaining metabolism or in the clearance of damaged proteins and organelles and the mitigation of oxidative stress. These findings illuminate the important role of metabolism in cancer progression and provide specific predictions for metabolic modulation in cancer therapy.

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