Genetic polymorphisms in inflammatory genes and pancreatic cancer risk: a two-phase study on more than 14 000 individuals.
Adenocarcinoma
/ genetics
Aged
Alleles
Biomarkers, Tumor
/ genetics
Carcinoma, Pancreatic Ductal
/ genetics
Case-Control Studies
Female
Genetic Predisposition to Disease
/ genetics
Genome-Wide Association Study
Genotype
Humans
Inflammation
/ genetics
Male
Odds Ratio
Pancreatic Neoplasms
/ genetics
Polymorphism, Single Nucleotide
/ genetics
Pancreatic Neoplasms
Journal
Mutagenesis
ISSN: 1464-3804
Titre abrégé: Mutagenesis
Pays: England
ID NLM: 8707812
Informations de publication
Date de publication:
19 12 2019
19 12 2019
Historique:
received:
28
08
2019
accepted:
18
10
2019
pubmed:
22
11
2019
medline:
24
6
2020
entrez:
22
11
2019
Statut:
ppublish
Résumé
There is overwhelming evidence that inflammation plays a key role in the pathogenesis of cancer and its progression. Inflammation is regulated through a complex network of genes and polymorphic variants in these genes have been found to be associated to risk of various human cancers, alone or in combination with environmental variables. Despite this, not much is known on the genetic variability of genes that regulate inflammation and risk of pancreatic ductal adenocarcinoma (PDAC). We performed a two-phase association study considering the genetic variability of 76 genes that are key players in inflammatory response. We analysed tagging single nucleotide polymorphisms (SNPs) and regulatory SNPs on 7207 PDAC cases and 7063 controls and observed several associations with PDAC risk. The most significant association was between the carriers of the A allele of the CCL4-rs1719217 polymorphism, which was reported to be also associated with the expression level of the CCL4 gene, and increased risk of developing PDAC (odds ratio = 1.12, 95% confidence interval = 1.06-1.18, P = 3.34 × 10-5). This association was significant also after correction for multiple testing, highlighting the importance of using potentially functional SNPs in order to discover more genetic variants associated with PDAC risk.
Identifiants
pubmed: 31748817
pii: 5636806
doi: 10.1093/mutage/gez040
doi:
Substances chimiques
Biomarkers, Tumor
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
395-401Informations de copyright
© The Author(s) 2019. Published by Oxford University Press on behalf of the UK Environmental Mutagen Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.