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SNP 1772 C > T of HIF-1α gene associates with breast cancer risk in a Taiwanese population

BACKGROUND: 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 reportedl...

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Detalles Bibliográficos
Autores principales: Huang, Chih-Jen, Lian, Shi-Long, Hou, Ming-Feng, Chai, Chee-Yin, Yang, Yi-Hsing, Lin, Sheng-Fung, Chang, Hsueh-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190286/
https://www.ncbi.nlm.nih.gov/pubmed/25302049
http://dx.doi.org/10.1186/s12935-014-0087-7
Descripción
Sumario:BACKGROUND: 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. RESULTS: 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 associated with clinicopathologic features of angiogenesis such as VEGF activity and the micro-vessel density and survival of breast cancer patients. CONCLUSION: Taken together, the 1772 C > T of HIF-1α gene is a potential biomarker for breast cancer susceptibility.