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A genetic variant rs13293512 in the promoter of let-7 is associated with an increased risk of breast cancer in Chinese women. | LitMetric

AI Article Synopsis

  • Recent research indicates that SNPs in miRNA promoters can affect disease susceptibility, specifically breast cancer.
  • The study focused on two SNPs, rs10877887 and rs13293512, assessing their association with breast cancer risk using DNA samples from 301 patients and 310 controls.
  • Findings revealed that the rs13293512 CC genotype is linked to a higher breast cancer risk, particularly in patients with negative hormone receptors and early-stage cancer, suggesting it may serve as a potential biomarker for breast cancer in Chinese women.

Article Abstract

Growing evidence has demonstrated that single-nucleotide polymorphisms (SNPs) in the promoter of miRNA may influence individuals' susceptibility to human diseases. We examined two SNPs rs10877887 and rs13293512 in the promoters of let-7 family to determine if the two SNPs were related to the occurrence of breast cancer (BC). Genotyping of the two SNPs was performed by PCR and restriction fragment length polymorphism analysis or TaqMan assay in 301 BC patients and 310 age matched controls. We found a higher frequency of rs13293512 CC genotype and rs13293512 C allele amongst BC patients (CC vs TT: adjusted odds ratio (OR) = 1.78; 95% CI: 1.14-2.80; =0.012; C vs T: adjusted OR = 1.33; 95% CI: 1.06-1.67; 0.013). Stratification analysis showed that rs13293512 CC genotype was associated with an increased risk of BC in patients with negative estrogen receptor (adjusted OR = 2.39; 95% CI: 1.32-4.30; 0.004), patients with negative progesterone receptor (adjusted OR = 1.92; 95% CI: 1.11-3.33; 0.02), patients with T1-2 stage cancer (adjusted OR = 1.77; 95% CI: 1.07-2.93; 0.03), and patients with N1-3 stage cancer (adjusted OR = 1.89; 95% CI: 1.13-3.17; 0.015). These findings suggest that rs13293512 in the promoter of let-7a-1/let-7f-1/let-7d cluster may be a possible biomarker for the development of BC in Chinese women.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6533205PMC
http://dx.doi.org/10.1042/BSR20182079DOI Listing

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