{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["7(47)"],"submitter":["Cox DG"],"pubmed_abstract":["Genetic polymorphisms are associated with breast cancer risk. Clinical and epidemiological observations suggest that clinical characteristics of breast cancer, such as estrogen receptor or HER2 status, are also influenced by hereditary factors. To identify genetic variants associated with pathological characteristics of breast cancer patients, a Genome Wide Association Study was performed in a cohort of 9365 women from the French nationwide SIGNAL/PHARE studies (NCT00381901/RECF1098). Strong association between the FGFR2 locus and ER status of breast cancer patients was observed (ER-positive n=6211, ER-negative n=2516; rs3135718 OR=1.34 p=5.46×10-12). This association was limited to patients with HER2-negative tumors (ER-positive n=4267, ER-negative n=1185; rs3135724 OR=1.85 p=1.16×10-11)."],"journal":["Oncotarget"],"pagination":["77358-77364"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC5363591"],"repository":["biostudies-literature"],"pubmed_title":["GWAS in the SIGNAL/PHARE clinical cohort restricts the association between the FGFR2 locus and estrogen receptor status to HER2-negative breast cancer patients."],"pmcid":["PMC5363591"],"pubmed_authors":["Soulie P","Rios M","Pauporte I","Levy C","Pivot X","Thomas G","Cojocarasu O","Boland A","Cox DG","Tarpin C","Trillet-Lenoir V","Faure-Mercier C","Ferrero JM","Bacq D","Tennevet I","Sahbatou M","Besse C","Meunier J","Curtit E","Mathieu MC","Bonnefoi H","Delecroix V","Blanche H","Jacquin JP","Assouline D","Deleuze JF","Lavau-Denes S","Fumoleau P","Bourgeois H","Romieu G","Darut-Jouve A","Pierga JY","Bachelot T","Jouannaud C","Petit T"],"additional_accession":[]},"is_claimable":false,"name":"GWAS in the SIGNAL/PHARE clinical cohort restricts the association between the FGFR2 locus and estrogen receptor status to HER2-negative breast cancer patients.","description":"Genetic polymorphisms are associated with breast cancer risk. Clinical and epidemiological observations suggest that clinical characteristics of breast cancer, such as estrogen receptor or HER2 status, are also influenced by hereditary factors. To identify genetic variants associated with pathological characteristics of breast cancer patients, a Genome Wide Association Study was performed in a cohort of 9365 women from the French nationwide SIGNAL/PHARE studies (NCT00381901/RECF1098). Strong association between the FGFR2 locus and ER status of breast cancer patients was observed (ER-positive n=6211, ER-negative n=2516; rs3135718 OR=1.34 p=5.46×10-12). This association was limited to patients with HER2-negative tumors (ER-positive n=4267, ER-negative n=1185; rs3135724 OR=1.85 p=1.16×10-11).","dates":{"release":"2016-01-01T00:00:00Z","publication":"2016 Nov","modification":"2026-05-05T10:18:32.762Z","creation":"2019-03-27T02:39:24Z"},"accession":"S-EPMC5363591","cross_references":{"pubmed":["27764800"],"doi":["10.18632/oncotarget.12669"]}}