Ontology highlight
ABSTRACT: Background
Colorectal cancer (CRC) is a major health concern worldwide. A series of sequential accumulation of genetic and epigenetic changes are responsible for the initiation and progression of diseases via the normal > adenoma > carcinoma sequence. Genetic variants in crucial cancer-causing genes are known to mediate the risk of cancer.Objective
In this case-control study, we examined single nucleotide polymorphism (SNP) in HER1 (rs763317 and rs3752651) and HER2 (rs1136201 and rs1058808) genes to assess their role in the susceptibility of CRC in a Saudi population.Methods
TaqMan allelic discrimination assay was utilized to identify the genotypes in 163 normal and 143 CRC patients.Results
In the overall analysis, the rs3752651 and rs1136201 were significan
SUBMITTER: Alanazi IO
PROVIDER: S-EPMC8553481 | biostudies-literature | 2021
REPOSITORIES: biostudies-literature