ASSOCIATION OF CDH1 -160 C/A (rs16260) POLYMORPHISM WITH METASTASIS IN BREAST CANCER
Keywords:
Breast Cancer, Metastasis, CDH1, Polymorphism, rs16260Abstract
Metastasis constitutes the primary cause of mortality in breast cancer, driven by the loss of intercellular adhesion and the activation of the Epithelial-to-Mesenchymal Transition (EMT). The CDH1 gene encodes E-cadherin, a critical tumor suppressor. The -160 C/A (rs16260) single nucleotide polymorphism (SNP) in the CDH1 promoter suppresses transcriptional activity, potentially influencing metastatic progression. However, data regarding this polymorphism in the specific patient population at Prof. dr. I.G.N.G. Ngoerah General Hospital remains unexplored. This study aimed to investigate the association between the CDH1 -160 C/A polymorphism and distant metastasis in breast cancer patients at Prof. dr. I.G.N.G. Ngoerah General Hospital. An observational analytic cross-sectional study was conducted using genomic DNA from 22 breast cancer patients, with genotyping performed via PCR and Sanger sequencing. Metastasis status (M0 vs. M1) was correlated with genotypes (Wild Type [CC] vs. Mutant [CA/AA]) using Fisher’s Exact Test and Odds Ratios (OR). The results indicated that the mutant genotypes (CA/AA) in this study population was high (86.4%). Of the 22 subjects, 4 (18.2%) had metastasis (M1). Statistical analysis showed no significant association between the CDH1 -160 C/A polymorphism genotype and metastasis status (Fisher's Exact Test, p-value = 0.073). In conclusion, no significant association was found between the CDH1 -160 C/A (rs16260) polymorphism and metastasis in breast cancer patients at Prof. dr. I.G.N.G. Ngoerah General Hospital.
Keywords: Breast Cancer, Metastasis, CDH1, Polymorphism, rs16260.







