Title of article :
Association of rs712 polymorphism in a let-7 microRNA-binding site of KRAS gene with colorectal cancer in a Mexican population
Author/Authors :
Gallegos-Arreola, Martha Patricia Centro de Investigación Biomédica de Occidente - Instituto Mexicano del Seguro Social - Guadalajara - Jalisco, México , Zúñiga-González, Guillermo Moisés Centro de Investigación Biomédica de Occidente - Instituto Mexicano del Seguro Social - Guadalajara - Jalisco, México , Gómez-Mariscal, Karen Centro de Investigación Biomédica de Occidente - Instituto Mexicano del Seguro Social - Guadalajara - Jalisco, México , Rosales-Reynoso, Mónica Alejandra Centro de Investigación Biomédica de Occidente - Instituto Mexicano del Seguro Social - Guadalajara - Jalisco, México , Figuera, Luis E Centro de Investigación Biomédica de Occidente - Instituto Mexicano del Seguro Social - Guadalajara - Jalisco, México , Puebla-Pérez, Ana María Laboratorio de Inmunofarmacología - Centro Universitario de Ciencias Exactas e Ingenierías - Universidad de Guadalajara - Guadalajara - Jalisco, Mexico , Pineda-Razo, Tomas Servicio de Oncología - Unidad Médica de Alta Especialidad - Hospital de Especialidades - Centro Médico Nacional de Occidente - Instituto Mexicano del Seguro Social - Guadalajara - Jalisco, Mexico
Abstract :
The rs712 polymorphism in a let-7 microRNA-binding site at KRAS gene has been
associated with cancer. To examine its association with rs712 polymorphism, we analyzed Mexican
individuals with colorectal cancer (CRC) and healthy subjects.
Materials and Methods: Genotyping of the rs712 polymorphism was performed by polymerase chain
reaction in 281 controls and 336 CRC patients.
Results: The observed frequencies of rs712 polymorphism indicated an associated protective factor
for CRC (P=0.032). An association between genotype and the disease was evident in: colon localization
(allele T, odds ratio (OR) 3.82, 95% confidence Intervals (CI) 2.77-5.28, P=0.0001), node metastasis
(genotype TT, or 2.49, 95% CI 1.45-4.28, P=0.0009), poor differentiation (genotype GT, or 2.35, 95%
CI 1.35-4.1, P=0.0033), and poor chemotherapy response (genotype GT, or 2.6, 95% CI 1.7-4.24,
P=0.0001).
Conclusion: Comparison of the data from patients with control group showed that polymorphism of
rs712 in KRAS gene was protective factor, which was associated with susceptibility for CRC. However,
the genotypes TT and GT of rs712 polymorphism in KRAS could contribute significantly to colon
localization, node metastasis, poor differentiation and poor chemotherapy response in CRC patients
in this sample population.
Keywords :
Colorectal cancer , KRAS , let-7 , Mexican population Polymorphism
Journal title :
Astroparticle Physics