抑制线粒体丙酮酸脱氢酶激酶:褪黑素引起癌细胞克服胞质糖酵解、减少肿瘤生物量和逆转对化疗不敏感的一种被提出的机制

R. Reiter, Ramaswamy Sharma, Q. Ma, S. Rosales‐Corral, D. Acuña-Castroviejo, G. Escames
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引用次数: 49

摘要

本文提出了一种假说来解释褪黑激素在调节癌细胞葡萄糖代谢中的作用。许多癌细胞利用胞质糖酵解(Warburg效应)来产生能量(ATP)。在这种情况下,葡萄糖主要转化为乳酸,并大量释放到血液中。在加速细胞增殖所需的增强大分子合成方面,Warburg效应赋予癌细胞优势,减少细胞凋亡,增加肿瘤生物量和更大的转移可能性。根据现有数据,夜间高循环褪黑激素水平是乳腺癌细胞从胞质糖酵解转向线粒体葡萄糖氧化和氧化磷酸化以产生ATP的信号。在这种情况下,褪黑素促进丙酮酸合成乙酰辅酶a;我们推测褪黑素通过抑制线粒体酶丙酮酸脱氢酶激酶(PDK)来实现这一点,PDK通常抑制丙酮酸脱氢酶复合物(PDC),这种酶控制丙酮酸转化为乙酰辅酶a。乙酰辅酶a在线粒体中有几个重要的功能;它进入柠檬酸循环,改善氧化磷酸化,此外,它是线粒体褪黑激素合成中限速酶芳基烷基胺n -乙酰转移酶的必要辅助因子。当乳腺癌细胞使用胞质糖酵解时(白天),它们具有癌症表型;在晚上,当它们利用线粒体通过氧化磷酸化产生ATP时,它们具有正常的细胞表型。如果这种肿瘤细胞代谢的昼夜差异在其他癌症中是常见的,这表明这些肿瘤细胞只是部分时间癌变。我们还推测夜间高褪黑素水平也能逆转肿瘤对化疗的不敏感。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibition of mitochondrial pyruvate dehydrogenase kinase: a proposed mechanism by which melatonin causes cancer cells to overcome cytosolic glycolysis, reduce tumor biomass and reverse insensitivity to chemotherapy
This review presents a hypothesis to explain the role of melatonin in regulating glucose metabolism in cancer cells.  Many cancer cells use cytosolic glycolysis (the Warburg effect) to produce energy (ATP).  Under these conditions, glucose is primarily converted to lactate which is released into the blood in large quantities. The Warburg effect gives cancer cells advantages in terms of enhanced macromolecule synthesis required for accelerated cellular proliferation, reduced cellular apoptosis which enhances tumor biomass and a greater likelihood of metastasis.  Based on available data, high circulating melatonin levels at night serve as a signal for breast cancer cells to switch from cytosolic glycolysis to mitochondrial glucose oxidation and oxidative phosphorylation for ATP production. In this situation, melatonin promotes the synthesis of acetyl-CoA from pyruvate; we speculate that melatonin does this by inhibiting the mitochondrial enzyme pyruvate dehydrogenase kinase (PDK) which normally inhibits pyruvate dehydrogenase complex (PDC), the enzyme that controls the pyruvate to acetyl-CoA conversion. Acetyl-CoA has several important functions in the mitochondria; it feeds into the citric acid cycle which improves oxidative phosphorylation and, additionally, it is a necessary co-factor for the rate limiting enzyme, arylalkylamine N-acetyltransferase, in mitochondrial melatonin synthesis.  When breast cancer cells are using cytosolic glycolysis (during the day) they are of the cancer phenotype; at night when they are using mitochondria to produce ATP via oxidative phosphorylation, they have a normal cell phenotype. If this day:night difference in tumor cell metabolism is common in other cancers, it indicates that these tumor cells are only cancerous part of the time.  We also speculate that high nighttime melatonin levels also reverse the insensitivity of tumors to chemotherapy.
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