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The relevance of tyrosine kinase inhibitors for global metabolic pathways in cancer

机译:酪氨酸激酶抑制剂与癌症总体代谢途径的相关性

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摘要

Tumor metabolism is a thrilling discipline that focuses on mechanisms used by cancer cells to earn crucial building blocks and energy to preserve growth and overcome resistance to various treatment modalities. At the same time, therapies directed specifically against aberrant signalling pathways driven by protein tyrosine kinases (TKs) involved in proliferation, metastasis and growth count for several years to promising anti-cancer approaches. In this respect, small molecule inhibitors are the most widely used clinically relevant means for targeted therapy, with a rising number of approvals for TKs inhibitors. In this review, we discuss recent observations related to TKs-associated metabolism and to metabolic feedback that is initialized as cellular response to particular TK-targeted therapies. These observations provide collective evidence that therapeutic responses are primarily linked to such pathways as regulation of lipid and amino acid metabolism, TCA cycle and glycolysis, advocating therefore the development of further effective targeted therapies against a broader spectrum of TKs to treat patients whose tumors display deregulated signalling driven by these proteins.
机译:肿瘤代谢是一门激动人心的学科,其重点是癌细胞用来赚取关键构件和能量以维持生长并克服对各种治疗方式的抵抗力的机制。同时,针对由蛋白质酪氨酸激酶(TK)驱动的异常信号转导途径的治疗,特别是针对涉及增殖,转移和生长的蛋白质,这种方法已经持续了数年之久,有望用于有前景的抗癌方法。在这方面,小分子抑制剂是最广泛用于靶向治疗的临床相关手段,TKs抑制剂的批准数量也在不断增加。在这篇综述中,我们讨论了与TK相关的新陈代谢和代谢反馈有关的最新观察结果,这些代谢反馈被初始化为对特定TK靶向疗法的细胞反应。这些观察提供了集体证据,表明治疗反应主要与脂质和氨基酸代谢,TCA循环和糖酵解的调节有关,因此主张针对更广泛的传统知识开发更有效的靶向疗法,以治疗肿瘤显示失调的患者这些蛋白质驱动的信号转导。

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