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Cancer-Induced Reprogramming of Host Glucose Metabolism: “Vicious Cycle” Supporting Cancer Progression

机译:癌症诱导的宿主葡萄糖代谢的重编程:“恶性循环”支持癌症进展

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摘要

Unrestricted cancer growth requires permanent supply of glucose that can be obtained from cancer-mediated reprogramming of glucose metabolism in the cancer-bearing host. The pathological mechanisms by which cancer cells exert their negative influence on host glucose metabolism are largely unknown. This paper proposes a mechanism of metabolic and hormonal changes that may favor glucose delivery to tumor (not host) cells by creating a cancer-host “vicious cycle” whose prolonged action drives cancer progression and promotes host cachexia. To verify this hypothesis, a feedback model of host-cancer interactions that create the “vicious cycle” via cancer-induced reprogramming of host glucose metabolism is proposed. This model is capable of answering some crucial questions as to how anabolic cancer cells can reprogram the systemic glucose metabolism and why these pathways were not observed in pregnancy. The current paper helps to better understanding a pathogenesis of cancer progression and identify hormonal/metabolic targets for anti-cancer treatment.
机译:不受限制的癌症生长需要葡萄糖的永久供应,这可以从患有癌症的宿主体内癌症介导的葡萄糖代谢重编程中获得。癌细胞对宿主葡萄糖代谢产生负面影响的病理机制尚不清楚。本文提出了一种代谢和激素变化的机制,该机制可能通过建立癌症-宿主“恶性循环”来促进葡萄糖向肿瘤(非宿主)细胞的传递,这种恶性循环的长期作用会驱动癌症进展并促进宿主恶病质。为了验证这一假设,提出了一种宿主-癌症相互作用的反馈模型,该模型通过癌症诱导的宿主葡萄糖代谢的重编程来创建“恶性循环”。该模型能够回答一些关键问题,如合成代谢癌细胞如何重编程全身性葡萄糖代谢以及为什么在怀孕期间未观察到这些途径。当前的文章有助于更好地了解癌症进展的发病机制,并确定激素/代谢靶点以进行抗癌治疗。

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