{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Zhang M"],"funding":["NIEHS NIH HHS","NCI NIH HHS"],"pagination":["594-609"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC4800000"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["183(6)"],"pubmed_abstract":["Hypoxia is a major cause of radiation resistance, which may predispose to local recurrence after radiation therapy. While hypoxia increases tumor cell survival after radiation exposure because there is less oxygen to oxidize damaged DNA, it remains unclear whether signaling pathways triggered by hypoxia contribute to radiation resistance. For example, intratumoral hypoxia can increase hypoxia inducible factor 1 alpha (HIF-1α), which may regulate pathways that contribute to radiation sensitization or radiation resistance. To clarify the role of HIF-1α in regulating tumor response to radiation, we generated a novel genetically engineered mouse model of soft tissue sarcoma with an intact or deleted HIF-1α. Deletion of HIF-1α sensitized primary sarcomas to radiation exposure in vivo. Moreover,"],"journal":["Radiation research"],"pubmed_title":["HIF-1 Alpha Regulates the Response of Primary Sarcomas to Radiation Therapy through a Cell Autonomous Mechanism."],"pmcid":["PMC4800000"],"funding_grant_id":["F30 CA180680","P30CA014236","R01 CA123350","R01CA169220","R01 ES005777","R01 CA169220","P30 CA014236"],"pubmed_authors":["Ilkayeva OR","Qiu Q","Sachdeva M","Ma Y","Zhang M","Rathmell JC","Han T","Dewhirst MW","Lui K","Nichols AG","Kirsch DG","Li Z","Min H","DeLaney TF","Cardona DM","Luo L","Kastan MB","Newgard CB"],"additional_accession":[]},"is_claimable":false,"name":"HIF-1 Alpha Regulates the Response of Primary Sarcomas to Radiation Therapy through a Cell Autonomous Mechanism.","description":"Hypoxia is a major cause of radiation resistance, which may predispose to local recurrence after radiation therapy. While hypoxia increases tumor cell survival after radiation exposure because there is less oxygen to oxidize damaged DNA, it remains unclear whether signaling pathways triggered by hypoxia contribute to radiation resistance. For example, intratumoral hypoxia can increase hypoxia inducible factor 1 alpha (HIF-1α), which may regulate pathways that contribute to radiation sensitization or radiation resistance. To clarify the role of HIF-1α in regulating tumor response to radiation, we generated a novel genetically engineered mouse model of soft tissue sarcoma with an intact or deleted HIF-1α. Deletion of HIF-1α sensitized primary sarcomas to radiation exposure in vivo. Moreover,","dates":{"release":"2015-01-01T00:00:00Z","publication":"2015 Jun","modification":"2025-04-22T12:00:44.396Z","creation":"2019-03-27T03:09:52Z"},"accession":"S-EPMC4800000","cross_references":{"pubmed":["25973951"],"doi":["10.1667/RR14016.1","10.1667/rr14016.1"]}}