模拟HIF在代谢关键基因LDH和PDH调控中的作用:Warburg表型的出现

Kévin Spinicci, Pierre Jacquet, Gibin Powathil, Angélique Stéphanou
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摘要

肿瘤的氧合作用及缺氧对肿瘤细胞代谢的影响是一个被广泛研究的课题。缺氧诱导因子(Hypoxia Inducible Factor, HIF)是细胞对缺氧反应的主要参与者,是癌症治疗的潜在靶点。HIF参与细胞增殖、存活、凋亡、血管生成、铁代谢、葡萄糖代谢等多种生物学过程。该蛋白调节乳酸脱氢酶(LDH)和丙酮酸脱氢酶(PDH)的表达,两者都是丙酮酸转化为有氧和厌氧途径所必需的。HIF上调乳酸脱氢酶,增加丙酮酸转化为乳酸,导致细胞分泌更多乳酸,降低微环境pH。HIF间接下调PDH,减少丙酮酸转化为乙酰辅酶A,从而减少有氧途径中三羧酸(TCA)循环的使用。即使在正常的细胞外氧条件下,HIF的上调也可能促进厌氧途径用于能量生产。即使在正常氧气条件下,糖酵解的高使用率也被称为沃伯格效应。在本文中,我们关注HIF在肿瘤生长过程中的变化,并通过数学模型研究其对两个代谢关键基因PDH和LDH的影响,以探讨其在Warburg效应出现中的作用。描述酶调控途径的数学方程在基于代理的模型中为肿瘤的每个细胞求解,以最好地捕捉肿瘤发展过程中由细胞消耗和肿瘤内扩散减少引起的时空氧变化。模拟结果表明,在常氧条件下降低HIF降解可以诱导更高的乳酸产量。沃伯格效应的出现出现在氧气条件恢复到正常水平之前的第一个缺氧期。结果还表明,针对LDH的上调和PDH的下调在治疗中可能是相关的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Modeling the role of HIF in the regulation of metabolic key genes LDH and PDH: Emergence of Warburg phenotype

Oxygenation of tumors and the effect of hypoxia on cancer cell metabolism is a widely studied subject. Hypoxia-inducible factor (HIF), the main actor in the cell response to hypoxia, represents a potential target in cancer therapy. HIF is involved in many biological processes such as cell proliferation, survival, apoptosis, angiogenesis, iron metabolism, and glucose metabolism. This protein regulates the expressions of lactate dehydrogenase (LDH) and pyruvate dehydrogenase (PDH), both essential for the conversion of pyruvate to be used in aerobic and anaerobic pathways. HIF upregulates LDH, increasing the conversion of pyruvate into lactate which leads to higher secretion of lactic acid by the cell and reduced pH in the microenvironment. HIF indirectly downregulates PDH, decreasing the conversion of pyruvate into acetyl coenzyme A, which leads to reduced usage of the tricarboxylic acid (TCA) cycle in aerobic pathways. Upregulation of HIF may promote the use of anaerobic pathways for energy production even in normal extracellular oxygen conditions. Higher use of glycolysis even in normal oxygen conditions is called the Warburg effect. In this paper, we focus on HIF variations during tumor growth and study, through a mathematical model, its impact on the two metabolic key genes PDH and LDH, to investigate its role in the emergence of the Warburg effect. Mathematical equations describing the enzyme regulation pathways were solved for each cell of the tumor represented in an agent-based model to best capture the spatio-temporal oxygen variations during tumor development caused by cell consumption and reduced diffusion inside the tumor. Simulation results show that reduced HIF degradation in normoxia can induce higher lactic acid production. The emergence of the Warburg effect appears after the first period of hypoxia before oxygen conditions return to a normal level. The results also show that targeting the upregulation of LDH and the downregulation of PDH could be relevant in therapy.

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审稿时长
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