{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Markkula A"],"funding":["Gunnar Nilsson Foundation","Medical Faculty at Lund University","Swedish Breast Cancer Group (BRO)","Mrs. Berta Kamprad Foundation","Lund Hospital Fund","Swedish Cancer Society","Konung Gustaf V:s Jubileumsfond,","South Swedish Health Care Region (Region Sk�ne ALF)","Swedish Research Council Formas"],"pagination":["1898-910"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC4225481"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["135(8)"],"pubmed_abstract":["The COX2 rs5277 (306G>C) polymorphism has been associated with inflammation-associated cancers. In breast cancer, tumor COX-2 expression has been associated with increased estrogen levels in estrogen receptor (ER)-positive and activated Akt-pathway in ER-negative tumors. Our study investigated the impact of COX2 genotypes on early breast cancer events and treatment response in relation to tumor ER status and body constitution. In Sweden, between 2002 and 2008, 634 primary breast cancer patients, aged 25-99 years, were included. Disease-free survival was assessed for 570 rs5277-genotyped patients. Body measurements and questionnaires were obtained preoperatively. Clinical data, patient- and tumor-characteristics were obtained from questionnaires, patients' charts, population registries and "],"journal":["International journal of cancer"],"pubmed_title":["Impact of COX2 genotype, ER status and body constitution on risk of early events in different treatment groups of breast cancer patients."],"pmcid":["PMC4225481"],"funding_grant_id":["CAN 2011/497","K2012-54X-22027-01-3"],"pubmed_authors":["Markkula A","Gaber A","Rosendahl AH","Jernstrom H","Ingvar C","Simonsson M","Rose C"],"additional_accession":[]},"is_claimable":false,"name":"Impact of COX2 genotype, ER status and body constitution on risk of early events in different treatment groups of breast cancer patients.","description":"The COX2 rs5277 (306G>C) polymorphism has been associated with inflammation-associated cancers. In breast cancer, tumor COX-2 expression has been associated with increased estrogen levels in estrogen receptor (ER)-positive and activated Akt-pathway in ER-negative tumors. Our study investigated the impact of COX2 genotypes on early breast cancer events and treatment response in relation to tumor ER status and body constitution. In Sweden, between 2002 and 2008, 634 primary breast cancer patients, aged 25-99 years, were included. Disease-free survival was assessed for 570 rs5277-genotyped patients. Body measurements and questionnaires were obtained preoperatively. Clinical data, patient- and tumor-characteristics were obtained from questionnaires, patients' charts, population registries and ","dates":{"release":"2014-01-01T00:00:00Z","publication":"2014 Oct","modification":"2025-04-27T00:54:07.13Z","creation":"2020-11-19T13:24:29Z"},"accession":"S-EPMC4225481","cross_references":{"pubmed":["24599585"],"doi":["10.1002/ijc.28831"]}}