{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Sun Z"],"funding":["Medical Research Council","ShanghaiTech University and the National Science Foundation of China"],"pagination":["1013-1024"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9359733"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["82(6)"],"pubmed_abstract":["The \"undruggable\" oncogene MYC supports cancer cell proliferation and survival through parallel induction of multiple anabolic processes. Here we find that inhibiting CTP synthase (CTPS) selectively decreases cell viability and induces DNA replication stress in MYC-overexpressing cells. MYC-driven rRNA synthesis caused the selective DNA replication stress upon CTPS inhibition. Combined inhibition of CTPS and ataxia telangiectasia and Rad3-related protein (ATR) is synthetically lethal in MYC-overexpressing cells, promoting cell death in vitro and decreasing tumor growth in vivo. Unexpectedly, interfering with CTPS1 but not CTPS2 is required to induce replication stress in MYC-deregulated cancer cells and consequent cell death in the presence of an ATR inhibitor. These results highlight a sp"],"journal":["Cancer research"],"pubmed_title":["Combined Inactivation of CTPS1 and ATR Is Synthetically Lethal to MYC-Overexpressing Cancer Cells."],"pmcid":["PMC9359733"],"funding_grant_id":["MC_UU_12021/3","MC_U137788471","81972632"],"pubmed_authors":["Zhang Z","Liu JL","Wang QQ","Sun Z"],"additional_accession":[]},"is_claimable":false,"name":"Combined Inactivation of CTPS1 and ATR Is Synthetically Lethal to MYC-Overexpressing Cancer Cells.","description":"The \"undruggable\" oncogene MYC supports cancer cell proliferation and survival through parallel induction of multiple anabolic processes. Here we find that inhibiting CTP synthase (CTPS) selectively decreases cell viability and induces DNA replication stress in MYC-overexpressing cells. MYC-driven rRNA synthesis caused the selective DNA replication stress upon CTPS inhibition. Combined inhibition of CTPS and ataxia telangiectasia and Rad3-related protein (ATR) is synthetically lethal in MYC-overexpressing cells, promoting cell death in vitro and decreasing tumor growth in vivo. Unexpectedly, interfering with CTPS1 but not CTPS2 is required to induce replication stress in MYC-deregulated cancer cells and consequent cell death in the presence of an ATR inhibitor. These results highlight a sp","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Mar","modification":"2025-04-22T04:22:24.373Z","creation":"2025-04-05T21:01:58.217Z"},"accession":"S-EPMC9359733","cross_references":{"pubmed":["35022212"],"doi":["10.1158/0008-5472.CAN-21-1707"]}}