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对癌细胞中的 SARS-CoV-2 进行基因组规模代谢建模,揭示了向糖酵解能量产生的增加转变。

Genome-scale metabolic modelling of SARS-CoV-2 in cancer cells reveals an increased shift to glycolytic energy production.

机构信息

School of Computing, Engineering and Digital Technologies, Teesside University, Middlesbrough, UK.

Department of Biology, University of Padua, Italy.

出版信息

FEBS Lett. 2021 Sep;595(18):2350-2365. doi: 10.1002/1873-3468.14180. Epub 2021 Sep 5.

Abstract

Cancer is considered a high-risk condition for severe illness resulting from COVID-19. The interaction between severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) and human metabolism is key to elucidating the risk posed by COVID-19 for cancer patients and identifying effective treatments, yet it is largely uncharacterised on a mechanistic level. We present a genome-scale map of short-term metabolic alterations triggered by SARS-CoV-2 infection of cancer cells. Through transcriptomic- and proteomic-informed genome-scale metabolic modelling, we characterise the role of RNA and fatty acid biosynthesis in conjunction with a rewiring in energy production pathways and enhanced cytokine secretion. These findings link together complementary aspects of viral invasion of cancer cells, while providing mechanistic insights that can inform the development of treatment strategies.

摘要

癌症被认为是 COVID-19 导致重症的高风险疾病。严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)与人体代谢之间的相互作用是阐明 COVID-19 给癌症患者带来的风险以及确定有效治疗方法的关键,但在机制层面上,这在很大程度上还没有被描述。我们提出了一个基于基因组规模的图谱,展示了 SARS-CoV-2 感染癌细胞引发的短期代谢改变。通过基于转录组和蛋白质组学的基因组规模代谢建模,我们描述了 RNA 和脂肪酸生物合成的作用,以及能量产生途径的重新布线和细胞因子分泌的增强。这些发现将癌细胞中病毒入侵的互补方面联系在一起,同时提供了可以为治疗策略的发展提供信息的机制见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4535/8427129/ca603f2710ce/FEB2-595-2350-g002.jpg

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