Ontology highlight
ABSTRACT: Background
Esophageal squamous cell carcinoma (ESCC) is very common in China and is also one of the most common cancers worldwide. The purpose of this study was to examine the associations between genetic variants of various cancer-related genes and the risk of ESCC.Methods
In this study, we first examined the association between 18 potentially disruptive genetic variants of 17 genes, including alcohol dehydrogenase 4 (ADH4) and checkpoint kinase 2 (CHEK2), and ESCC risk in a Hangzhou population of 617 patients matched with 534 controls. Among the 18 single nucleotide polymorphisms (SNPs), two were validated in a Jinan population of 540 patients matched with 550 controls.Results
Sixteen SNPs in 15 genes, including CHEK2, did not have significantly different allele f
SUBMITTER: Xu X
PROVIDER: S-EPMC4454665 | biostudies-literature | 2015
REPOSITORIES: biostudies-literature