<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Larsen V</submitter><funding>Breast Cancer Research Foundation</funding><funding>Susan G. Komen Foundation</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIH</funding><pagination>225-235.e2</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6667288</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>19(4)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>GATA3 is a critical transcription factor in maintaining the differentiated state of luminal mammary epithelial cells. We sought to determine the prognostic and predictive roles of GATA3 genotypes for breast cancer.&lt;h4>Patients and methods&lt;/h4>Twelve single nucleotide polymorphisms (SNPs) were genotyped in 2 breast cancer cohorts, including the SWOG S8897 trial where patients were treated with adjuvant chemotherapy (CAF [cyclophosphamide, doxorubicin, 5-fluorouracil] vs. CMF [cyclophosphamide, methotrexate, 5-fluorouracil]) or untreated, and the observational Pathways Study.&lt;h4>Results&lt;/h4>In the S8897 trial, rs3802604 and rs568727 were associated with disease-free survival and overall survival in the treated group, regardless of chemotherapy regimen. The GG genotype of</pubmed_abstract><journal>Clinical breast cancer</journal><pubmed_title>Germline Genetic Variants in GATA3 and Breast Cancer Treatment Outcomes in SWOG S8897 Trial and the Pathways Study.</pubmed_title><pmcid>PMC6667288</pmcid><funding_grant_id>UG1 CA189821</funding_grant_id><funding_grant_id>U10 CA180819</funding_grant_id><funding_grant_id>P30 CA016056</funding_grant_id><funding_grant_id>UG1 CA189830</funding_grant_id><funding_grant_id>R01 CA105274</funding_grant_id><funding_grant_id>U01 CA195565</funding_grant_id><funding_grant_id>U10 CA180801</funding_grant_id><funding_grant_id>UG1 CA233160</funding_grant_id><funding_grant_id>U10 CA180888</funding_grant_id><funding_grant_id>U24 CA171524</funding_grant_id><pubmed_authors>Ravdin PM</pubmed_authors><pubmed_authors>Roh JM</pubmed_authors><pubmed_authors>Hortobagyi GN</pubmed_authors><pubmed_authors>Osborne CK</pubmed_authors><pubmed_authors>Hutchins LF</pubmed_authors><pubmed_authors>Yao S</pubmed_authors><pubmed_authors>Kushi LH</pubmed_authors><pubmed_authors>Liu S</pubmed_authors><pubmed_authors>Kwan ML</pubmed_authors><pubmed_authors>Yang JJ</pubmed_authors><pubmed_authors>Yeh IT</pubmed_authors><pubmed_authors>Ergas IJ</pubmed_authors><pubmed_authors>Barlow WE</pubmed_authors><pubmed_authors>Larsen V</pubmed_authors><pubmed_authors>Albain KS</pubmed_authors><pubmed_authors>Hayes DF</pubmed_authors><pubmed_authors>Martino S</pubmed_authors><pubmed_authors>Zhu Q</pubmed_authors><pubmed_authors>Ambrosone CB</pubmed_authors><pubmed_authors>Kadlubar SA</pubmed_authors><pubmed_authors>Rae JM</pubmed_authors><pubmed_authors>Lyss AP</pubmed_authors></additional><is_claimable>false</is_claimable><name>Germline Genetic Variants in GATA3 and Breast Cancer Treatment Outcomes in SWOG S8897 Trial and the Pathways Study.</name><description>&lt;h4>Introduction&lt;/h4>GATA3 is a critical transcription factor in maintaining the differentiated state of luminal mammary epithelial cells. We sought to determine the prognostic and predictive roles of GATA3 genotypes for breast cancer.&lt;h4>Patients and methods&lt;/h4>Twelve single nucleotide polymorphisms (SNPs) were genotyped in 2 breast cancer cohorts, including the SWOG S8897 trial where patients were treated with adjuvant chemotherapy (CAF [cyclophosphamide, doxorubicin, 5-fluorouracil] vs. CMF [cyclophosphamide, methotrexate, 5-fluorouracil]) or untreated, and the observational Pathways Study.&lt;h4>Results&lt;/h4>In the S8897 trial, rs3802604 and rs568727 were associated with disease-free survival and overall survival in the treated group, regardless of chemotherapy regimen. The GG genotype of</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Aug</publication><modification>2026-04-29T17:45:51.417Z</modification><creation>2020-09-11T07:22:16Z</creation></dates><accession>S-EPMC6667288</accession><cross_references><pubmed>30928413</pubmed><doi>10.1016/j.clbc.2019.02.010</doi></cross_references></HashMap>