AI Article Synopsis

  • - Breast cancer is a common disease in women worldwide, and this study looked at the role of specific genetic variations (SNPs) in increasing susceptibility to the disease in a Chilean population.
  • - The research found no link between two of the SNPs (rs2910164 and rs3746444) and breast cancer risk, while a specific variant (rs2043556-C) was associated with a decreased risk, particularly for those with a family history of the disease.
  • - Additionally, the SNP rs4541843-T was linked to an increased risk of familial breast cancer, and a combination of risk alleles showed a cumulative effect, suggesting a higher likelihood of developing the disease as more risk alleles are present

Article Abstract

Breast cancer (BC) is one of the most frequent tumors affecting women worldwide. microRNAs (miRNAs) single-nucleotide polymorphisms (SNPs) likely contribute to BC susceptibility. We evaluated the association of five SNPs with BC risk in non-carriers of the -mutation from a South American population. The SNPs were genotyped in 440 Chilean -negative BC cases and 1048 controls. Our data do not support an association between rs2910164:G>C or rs3746444:A>G and BC risk. The rs12975333:G>T is monomorphic in the Chilean population. The pre-miR-605 rs2043556-C allele was associated with a decreased risk of BC, both in patients with a strong family history of BC and in early-onset non-familial BC (Odds ratio (OR) = 0.5 [95% confidence interval (CI) 0.4⁻0.9] = 0.006 and OR = 0.6 [95% CI 0.5⁻0.9] = 0.02, respectively). The rs4541843-T allele is associated with increased risk of familial BC. This is the first association study on rs4541843 and BC risk. Previously, we showed that the -rs3803662:C>T was significantly associated with increased risk of familial BC. Given that mRNA is a target of miR-182, and that both the rs3803662-T and pri-miR-182 rs4541843-T alleles are associated with increased BC risk, we evaluated their combined effect. Risk of familial BC increased in a dose-dependent manner with the number of risk alleles (-trend = 0.0005), indicating an additive effect.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6162394PMC
http://dx.doi.org/10.3390/genes9090427DOI Listing

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