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甲酸盐诱导核苷酸和能量代谢的代谢转换。

Formate induces a metabolic switch in nucleotide and energy metabolism.

机构信息

Cancer Research UK Beatson Institute, Glasgow, UK.

Center of Molecular Immunology, Havana, Cuba.

出版信息

Cell Death Dis. 2020 May 4;11(5):310. doi: 10.1038/s41419-020-2523-z.

Abstract

Formate is a precursor for the de novo synthesis of purine and deoxythymidine nucleotides. Formate also interacts with energy metabolism by promoting the synthesis of adenine nucleotides. Here we use theoretical modelling together with metabolomics analysis to investigate the link between formate, nucleotide and energy metabolism. We uncover that endogenous or exogenous formate induces a metabolic switch from low to high adenine nucleotide levels, increasing the rate of glycolysis and repressing the AMPK activity. Formate also induces an increase in the pyrimidine precursor orotate and the urea cycle intermediate argininosuccinate, in agreement with the ATP-dependent activities of carbamoyl-phosphate and argininosuccinate synthetase. In vivo data for mouse and human cancers confirms the association between increased formate production, nucleotide and energy metabolism. Finally, the in vitro observations are recapitulated in mice following and intraperitoneal injection of formate. We conclude that formate is a potent regulator of purine, pyrimidine and energy metabolism.

摘要

甲酸盐是嘌呤和脱氧胸苷核苷酸从头合成的前体。甲酸盐还通过促进腺嘌呤核苷酸的合成与能量代谢相互作用。在这里,我们使用理论建模和代谢组学分析来研究甲酸盐、核苷酸和能量代谢之间的联系。我们揭示了内源性或外源性甲酸盐诱导从低到高腺嘌呤核苷酸水平的代谢转换,增加糖酵解的速率并抑制 AMPK 活性。甲酸盐还诱导嘧啶前体乳清酸和尿素循环中间物精氨酸琥珀酸的增加,这与氨甲酰磷酸和精氨酸琥珀酸合成酶的 ATP 依赖性活性一致。来自小鼠和人类癌症的体内数据证实了增加的甲酸盐产生、核苷酸和能量代谢之间的关联。最后,在小鼠腹腔内注射甲酸盐后,在体外观察到了类似的结果。我们得出结论,甲酸盐是嘌呤、嘧啶和能量代谢的有效调节剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b17e/7198490/d172ca718b90/41419_2020_2523_Fig1_HTML.jpg

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