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Balancing glycolytic flux: the role of 6-phosphofructo-2-kinase/fructose 2,6-bisphosphatases in cancer metabolism

机译:平衡糖酵解通量:6-磷酸果糖-2-激酶/果糖2,6-双磷酸酶在癌症代谢中的作用

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The increased glucose metabolism in cancer cells is required to fulfill their high energetic and biosynthetic demands. Changes in the metabolic activity of cancer cells are caused by the activation of oncogenes or loss of tumor suppressors. They can also be part of the metabolic adaptations to the conditions imposed by the tumor microenvironment, such as the hypoxia response. Among the metabolic enzymes that are modulated by these factors are the 6-phosphofructo-2-kinase/fructose 2,6-bisphosphatases (PFKFBs), a family of bifunctional enzymes that control the levels of fructose 2,6-bisphosphate (Fru-2,6-P2). This metabolite is important for the dynamic regulation of glycolytic flux by allosterically activating the rate-limiting enzyme of glycolysis phosphofructokinase-1 (PFK-1). Therapeutic strategies designed to alter the levels of this metabolite are likely to interfere with the metabolic balance of cancer cells, and could lead to a reduction in cancer cell proliferation, invasiveness and survival. This article will review our current understanding of the role of PFKFB proteins in the control of cancer metabolism and discuss the emerging interest in these enzymes as potential targets for the development of antineoplastic agents.
机译:需要癌细胞中增加的葡萄糖代谢来满足其高能量和生物合成需求。癌细胞代谢活性的变化是由癌基因的激活或抑癌基因的丧失引起的。它们也可以是对肿瘤微环境所施加条件(例如低氧反应)的代谢适应的一部分。在受这些因素调节的代谢酶中,有6-磷酸果糖-2-激酶/果糖2,6-双磷酸酶(PFKFBs),这是一种控制果糖2,6-双磷酸(Fru-2)水平的双功能酶家族。 ,6-P 2 )。该代谢物通过变构活化糖酵解磷酸果糖激酶-1(PFK-1)的限速酶,对于动态调节糖酵解通量很重要。设计用来改变这种代谢物水平的治疗策略可能会干扰癌细胞的代谢平衡,并可能导致癌细胞增殖,侵袭性和存活率降低。本文将回顾我们目前对PFKFB蛋白在癌症代谢控制中的作用的了解,并讨论对这些酶作为抗肿瘤药开发潜在靶点的兴趣。

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