{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Li MX"],"funding":["Chinese Ministry of Science and Technology | Department of S and T for Social Development","National Natural Science Foundation of China"],"pagination":["492"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10397262"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["14(8)"],"pubmed_abstract":["Metabolic heterogeneity of tumor microenvironment (TME) is a hallmark of cancer and a big barrier to cancer treatment. Cancer cells display diverse capacities to utilize alternative carbon sources, including nucleotides, under poor nutrient circumstances. However, whether and how purine, especially inosine, regulates mitochondrial metabolism to buffer nutrient starvation has not been well-defined yet. Here, we identify the induction of 5'-nucleotidase, cytosolic II (NT5C2) gene expression promotes inosine accumulation and maintains cancer cell survival in the nutrient-poor region. Inosine elevation further induces Rag GTPases abundance and mTORC1 signaling pathway by enhancing transcription factor SP1 level in the starved tumor. Besides, inosine supplementary stimulates the synthesis of na"],"journal":["Cell death & disease"],"pubmed_title":["Inosine enhances tumor mitochondrial respiration by inducing Rag GTPases and nascent protein synthesis under nutrient starvation."],"pmcid":["PMC10397262"],"funding_grant_id":["32270827, 82203590","2021YFA0804803"],"pubmed_authors":["Li MX","Wu XT","Hu S","Jing WQ","Hou WK","Yan W"],"additional_accession":[]},"is_claimable":false,"name":"Inosine enhances tumor mitochondrial respiration by inducing Rag GTPases and nascent protein synthesis under nutrient starvation.","description":"Metabolic heterogeneity of tumor microenvironment (TME) is a hallmark of cancer and a big barrier to cancer treatment. Cancer cells display diverse capacities to utilize alternative carbon sources, including nucleotides, under poor nutrient circumstances. However, whether and how purine, especially inosine, regulates mitochondrial metabolism to buffer nutrient starvation has not been well-defined yet. Here, we identify the induction of 5'-nucleotidase, cytosolic II (NT5C2) gene expression promotes inosine accumulation and maintains cancer cell survival in the nutrient-poor region. Inosine elevation further induces Rag GTPases abundance and mTORC1 signaling pathway by enhancing transcription factor SP1 level in the starved tumor. Besides, inosine supplementary stimulates the synthesis of na","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023 Aug","modification":"2025-07-02T03:04:37.302Z","creation":"2025-07-02T03:04:37.302Z"},"accession":"S-EPMC10397262","cross_references":{"pubmed":["37532694"],"doi":["10.1038/s41419-023-06017-2"]}}