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The regulation of energy generating metabolic pathways by p53.

机译:p53对能量代谢途径的调节。

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The function of p53 as a tumor suppressor remains undisputed. p53 has a central role in cellular stress responses as well as affecting cancer development and progression. The word "central", however, is becoming increasingly more of an understatement as the list of p53-regulated pathways and processes is ever expanding. Although much focus continues to center on p53-mediated signaling cascades that control cell growth arrest and/or apoptosis, recent work has begun to define a role for p53 in the regulation of metabolic pathways typically thought of as essential for maintaining life. With the first potential link between p53 and glycolysis reported nearly ten years ago, the topic has gained a renewed interest. Recent studies now demonstrate the ability of p53 to regulate the expression of several novel genes including PGM (phosphoglycerate mutase), TIGAR (TP53-induced glycolysis and apoptosis regulator) and, SCO2 (synthesis of cytochrome c oxidase 2), each intimately linked to the processes of glycolysis and oxidative phosphorylation. With this discovery, yet another novel means by which p53 carries out its tumor suppressor function is brought into light.
机译:p53作为肿瘤抑制物的功能尚无争议。 p53在细胞应激反应以及影响癌症发展和进程中起着核心作用。然而,随着p53调控的途径和过程的清单不断扩大,“中央”一词正变得越来越轻描淡写。尽管许多注意力仍然集中在控制细胞生长停滞和/或凋亡的p53介导的信号级联反应上,但最近的工作已开始确定p53在代谢途径调节中的作用,通常认为代谢途径对于维持生命至关重要。大约十年前,报道了p53和糖酵解之间的第一个潜在联系,这一话题引起了新的兴趣。现在的最新研究表明,p53调节几种新基因表达的能力,包括PGM(磷酸甘油酸突变酶),TIGAR(TP53诱导的糖酵解和细胞凋亡调节剂)和SCO2(细胞色素c氧化酶2的合成),每个都密切相关。糖酵解和氧化磷酸化的过程。通过该发现,揭示了p53执行其肿瘤抑制功能的另一种新颖的方法。

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