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ADIPOQ single nucleotide polymorphisms and breast cancer in northeastern Mexican women

BACKGROUND: Adiponectin gene (ADIPOQ) polymorphisms have been shown to affect adiponectin serum concentration and some have been associated with breast cancer (BC) risk. The aims of this study were to describe the frequency of single nucleotide polymorphisms (SNPs) of ADIPOQ in Mexican women with BC...

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Detalles Bibliográficos
Autores principales: Cerda-Flores, Ricardo M., Camarillo-Cárdenas, Karen Paola, Gutiérrez-Orozco, Gabriela, Villarreal-Vela, Mónica Patricia, Garza-Guajardo, Raquel, Ponce-Camacho, Marco Antonio, Castruita-Ávila, Ana Lilia, González-Guerrero, Juan Francisco, Rodríguez-Sánchez, Iram Pablo, Calderón-Garcidueñas, Ana Laura, Rodríguez-Gutierrez, Hazyadee Frecia, Arellano-Barrientos, Juan Carlos, Gutierrez, Oscar Vidal, Saldaña, Hugo Alberto Barrera, Garza-Rodríguez, María Lourdes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519484/
https://www.ncbi.nlm.nih.gov/pubmed/32977760
http://dx.doi.org/10.1186/s12881-020-01125-8
Descripción
Sumario:BACKGROUND: Adiponectin gene (ADIPOQ) polymorphisms have been shown to affect adiponectin serum concentration and some have been associated with breast cancer (BC) risk. The aims of this study were to describe the frequency of single nucleotide polymorphisms (SNPs) of ADIPOQ in Mexican women with BC and to determine if they show an association with it. METHODS: DNA samples from 397 patients and 355 controls were tested for the ADIPOQ gene SNPs: rs2241766 (GT) and rs1501299 (GT) by TaqMan allelic discrimination assay. Hardy–Weinberg equilibrium (HWE) was tested. Multiple SNP inheritance models adjusted by age and body mass index (BMI) were examined for the SNP rs1501299. RESULTS: We found that in the frequency analysis of rs1501299 without adjusting the BMI and age, the genotype distribution had a statistically significant difference (P = 0.003). The T allele was associated with a BC risk (OR, 1.99; 95% CI 1.13–3.51, TT vs. GG; OR, 1.53; 95% CI 1.12–2.09, GT vs. GG). The SNP rs2241766 was in HW disequilibrium in controls. In conclusion, the rs1501299 polymorphism is associated with a BC risk. CONCLUSIONS: Identification of the genotype of these polymorphisms in patients with BC can contribute to integrate the risk profile in both patients and their relatives as part of a comprehensive approach and increasingly more personalized medicine.