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转酮醇酶样1在肿瘤代谢重编程中的关键作用。

A key role for transketolase-like 1 in tumor metabolic reprogramming.

作者信息

Diaz-Moralli Santiago, Aguilar Esther, Marin Silvia, Coy Johannes F, Dewerchin Mieke, Antoniewicz Maciek R, Meca-Cortés Oscar, Notebaert Leen, Ghesquière Bart, Eelen Guy, Thomson Timothy M, Carmeliet Peter, Cascante Marta

机构信息

Department of Biochemistry and Molecular Biomedicine, Faculty of Biology, Universitat de Barcelona, Barcelona, Spain.

Institute of Biomedicine of Universitat de Barcelona (IBUB) and CSIC-Associated Unit, Barcelona, Spain.

出版信息

Oncotarget. 2016 Aug 9;7(32):51875-51897. doi: 10.18632/oncotarget.10429.

Abstract

Metabolic reprogramming, a crucial cancer hallmark, shifts metabolic pathways such as glycolysis, tricarboxylic acid cycle or lipogenesis, to enable the growth characteristics of cancer cells. Here, we provide evidence that transketolase-like 1 (TKTL1) orchestrates aerobic glycolysis, fatty acid and nucleic acid synthesis, glutamine metabolism, protection against oxidative stress and cell proliferation. Furthermore, silencing of TKTL1 reduced the levels of sphingolipids such as lactosylceramide (a sphingolipid regulating cell survival, proliferation and angiogenesis) and phosphatidylinositol (which activates PI3K/Akt/mTOR signaling). Thus, in addition to its well-known roles in glucose and amino acid metabolism, TKTL1 also regulates lipid metabolism. In conclusion, our study provides unprecedented evidence that TKTL1 plays central roles in major metabolic processes subject to reprogramming in cancer cells and thus identifies TKTL1 as a promising target for new anti-cancer therapies.

摘要

代谢重编程是癌症的一个关键特征,它会改变糖酵解、三羧酸循环或脂肪生成等代谢途径,以实现癌细胞的生长特性。在此,我们提供证据表明,转酮醇酶样1(TKTL1)协调有氧糖酵解、脂肪酸和核酸合成、谷氨酰胺代谢、抗氧化应激以及细胞增殖。此外,沉默TKTL1可降低鞘脂水平,如乳糖神经酰胺(一种调节细胞存活、增殖和血管生成的鞘脂)和磷脂酰肌醇(激活PI3K/Akt/mTOR信号传导)。因此,除了在葡萄糖和氨基酸代谢中的已知作用外,TKTL1还调节脂质代谢。总之,我们的研究提供了前所未有的证据,表明TKTL1在癌细胞中经历重编程的主要代谢过程中发挥核心作用,因此将TKTL1确定为新的抗癌疗法的一个有前景的靶点。

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