Association of rs712 polymorphism in a let-7 microRNA-binding site of KRAS gene with colorectal cancer in a Mexican population

被引:11
|
作者
Patricia Gallegos-Arreola, Martha [1 ]
Moises Zuniga-Gonzalez, Guillermo [2 ]
Gomez-Mariscal, Karen [2 ]
Alejandra Rosales-Reynoso, Monica [2 ]
Figuera, Luis E. [1 ]
Maria Puebla-Perez, Ana [3 ]
Pineda-Razo, Tomas [4 ]
机构
[1] Inst Mexicano Seguro Social, Div Genet, Ctr Invest Biomed Occidente, Sierra Mojada 800, Guadalajara 44340, Jalisco, Mexico
[2] Inst Mexicano Seguro Social, Ctr Invest Biomed Occidente, Med Mol, Guadalajara, Jalisco, Mexico
[3] Univ Guadalajara, Ctr Univ Ciencias Exactas & Ingn, Lab Inmunofarmacol, Guadalajara, Jalisco, Mexico
[4] Inst Mexicano Seguro Social, Hosp Especialidades, Ctr Med Nacl Occidente, Serv Oncol,Unidad Med Alta Especialidad, Guadalajara, Jalisco, Mexico
关键词
Colorectal cancer; KRAS; let-7; Mexican population; Polymorphism; MUTATION;
D O I
10.22038/ijbms.2019.26564.6507
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objective(s): 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.
引用
收藏
页码:324 / 327
页数:4
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