Biomedicines (Mar 2024)

Association of the rs1966265 and rs351855 <i>FGFR4</i> Variants with Colorectal Cancer in a Mexican Population and Their Analysis In Silico

  • Irving Alejandro Carrillo-Dávila,
  • Asbiel Felipe Garibaldi-Ríos,
  • Luis E. Figuera,
  • Belinda Claudia Gómez-Meda,
  • Guillermo M. Zúñiga-González,
  • Ana María Puebla-Pérez,
  • Patricia Montserrat García-Verdín,
  • Paola Beatriz Castro-García,
  • Itzae Adonai Gutiérrez-Hurtado,
  • Blanca Miriam Torres-Mendoza,
  • Martha Patricia Gallegos-Arreola

DOI
https://doi.org/10.3390/biomedicines12030602
Journal volume & issue
Vol. 12, no. 3
p. 602

Abstract

Read online

The aim of this study was to associate FGFR4 rs1966265 and rs351855 variants with colorectal cancer (CRC) in a Mexican population and to perform in silico analysis. Genomic DNA from 412 healthy individuals and 475 CRC patients was analyzed. In silico analysis was performed using the PolyPhen-V2, GEPIA, GTEx, and Cytoscape platforms. The GA genotype dominant model (GAAA) of rs1966265 and the AA genotype dominant and recessive models of rs351855 were identified as CRC risk factors (p p p p EFNA4, SLC3A2, and HNF1A share signaling pathways with FGFR4. Therefore, rs1966265 and rs351855 may be potential CRC risk factors.

Keywords