<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(1)</volume><submitter>Huang CJ</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Hypoxia inducible factor 1α (HIF-1α) is a stress-responsive transcription factor to hypoxia and its expression is correlated to tumor progression and angiogenesis. Several single nucleotide polymorphisms (SNPs) of HIF-1α gene in the oxygen-dependent degradation (ODD) domain was reportedly associated with increased HIF-1α activity.&lt;h4>Results&lt;/h4>In this study, we focused on the relationship between SNP 1772 C > T (rs11549465) of HIF-1α gene and its breast cancer risk, as well as its correlation with HIF-1α expression and tumor angiogenesis. Ninety six breast cancer patients and 120 age-matched controls were enrolled. We found that 1772 T allele of HIF-1α gene was associated with increased breast cancer risk (adjusted OR = 14.51; 95% CI: 6.74-31.24). This SNP was not asso</pubmed_abstract><journal>Cancer cell international</journal><pagination>87</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4190286</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>SNP 1772 C > T of HIF-1α gene associates with breast cancer risk in a Taiwanese population.</pubmed_title><pmcid>PMC4190286</pmcid><pubmed_authors>Lian SL</pubmed_authors><pubmed_authors>Yang YH</pubmed_authors><pubmed_authors>Chang HW</pubmed_authors><pubmed_authors>Hou MF</pubmed_authors><pubmed_authors>Lin SF</pubmed_authors><pubmed_authors>Chai CY</pubmed_authors><pubmed_authors>Huang CJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>SNP 1772 C > T of HIF-1α gene associates with breast cancer risk in a Taiwanese population.</name><description>&lt;h4>Background&lt;/h4>Hypoxia inducible factor 1α (HIF-1α) is a stress-responsive transcription factor to hypoxia and its expression is correlated to tumor progression and angiogenesis. Several single nucleotide polymorphisms (SNPs) of HIF-1α gene in the oxygen-dependent degradation (ODD) domain was reportedly associated with increased HIF-1α activity.&lt;h4>Results&lt;/h4>In this study, we focused on the relationship between SNP 1772 C > T (rs11549465) of HIF-1α gene and its breast cancer risk, as well as its correlation with HIF-1α expression and tumor angiogenesis. Ninety six breast cancer patients and 120 age-matched controls were enrolled. We found that 1772 T allele of HIF-1α gene was associated with increased breast cancer risk (adjusted OR = 14.51; 95% CI: 6.74-31.24). This SNP was not asso</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014</publication><modification>2025-04-18T16:59:01.649Z</modification><creation>2019-03-27T01:37:15Z</creation></dates><accession>S-EPMC4190286</accession><cross_references><pubmed>25302049</pubmed><doi>10.1186/s12935-014-0087-7</doi></cross_references></HashMap>