Journal of Breast Cancer · 2018 · 18 citations · 25 references
Life SciencesGeneticsOncologyCancer GeneticsHuman GeneticsMedical GeneticsGenome-wide Association StudiesGenotype-phenotype Association AnalysisHer2-positive Breast CancerAxillary Lymph Node Involvement AssessmentBreast Cancer GenomicsBreast Cancer HistologyBreast Cancer HistopathologyBreast Cancer Molecular SubtypesCommon Genetic VariantsEstrogen Receptor StatusGenetic Risk Variants
PURPOSE: Several single nucleotide polymorphisms (SNPs) have been reported to be associated with clinicopathological profiles in sporadic breast cancer based on studies conducted on major population groups. The knowledge of the effects of these common genetic variants in South Asian populations remains limited. The present study aimed to investigate the association between a selected set of SNPs and the clinicopathological profiles in sporadic breast cancer in Sri Lankan women. METHODS: A total of 350 postmenopausal women with histologically confirmed invasive breast cancer were genotyped for 58 SNPs located in 36 breast cancer related genes. The clinicopathological factors that were investigated included age of onset, tumor histologic grade, and lymph node involvement, as well as estrogen receptor (ER), progesterone receptor, and human epidermal growth factor receptor 2 (HER2) status. Association testing was performed using logistic regression models adjusted for confounding factors. RESULTS: =0.041) were associated with high tumor histologic grade. CONCLUSION: genes could serve as potential clinical and prognostic biomarkers in sporadic breast cancer patients. Further studies are required to validate our current findings in other populations.
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Pieter J.A. Eichhorn, Magüi Gili, Maurizio Scaltriti et al. · Cancer Research · 2008 · 494 citations · Full text
Medicine, Oncology, Pharmacology +17