Lack of Association between Epidermal Growth Factor or Its Receptor and Reflux Esophagitis, Barrett's Esophagus, and Esophageal Adenocarcinoma: A Case-Control Study. (31st August 2022)

• Record Type: Journal Article
• Authors: Deissova, Tereza; Cvanova, Michaela; Kala, Zdenek; Jiraskova Zakostelska, Zuzana; Dolina, Jiri; Kunovsky, Lumir; Kroupa, Radek; Pavlovsky, Zdenek; Lipovy, Bretislav; Danek, Zdenek; Izakovicova Holla, Lydie; Urban, Ondrej; Navratil, Vit; Lischke, Robert; Harustiak, Tomas; Grolich, Tomas; Prochazka, Vladimir; Slaby, Ondrej; Borilova Linhartova, Petra
• Other Names: Malaguarnera Michele Academic Editor.
• Is Part Of: Disease markers. Volume 2022(2022)
• Publication Date: 2022-08-31
• Subjects: Diagnosis -- Periodicals; Biochemical markers -- Periodicals; Pathology -- Periodicals; 616
• DOI: 10.1155/2022/8790748
• Languages: English
• ISSNs: 0278-0240

Abstract

Abstract : The epidermal growth factor ( EGF ) and its receptor ( EGFR ) gene-gene interactions were shown to increase the susceptibility to esophageal cancer. However, the role of the EGF/EGFR pathway in the development of gastroesophageal reflux disease (GERD) and its complications (reflux esophagitis (RE), Barrett's esophagus (BE), and esophageal adenocarcinoma (EAC)) remains unclear. This association study is aimed at investigating functional EGF and EGFR gene polymorphisms, their mRNA expression in esophageal tissues, and EGF plasma levels in relation to RE, BE, and EAC development in the Central European population. 301 patients with RE/BE/EAC (cases) as well as 98 patients with nonerosive reflux disease (NERD) and 8 healthy individuals (controls) were genotyped for +61 A>G EGF (rs4444903) and +142285 G>A EGFR (rs2227983) polymorphisms using the TaqMan quantitative polymerase chain reaction (qPCR). In random subgroups, the EGF and EGFR mRNA expressions were analyzed by reverse transcription qPCR in esophageal tissue with and without endoscopically visible pathological changes; and the EGF plasma levels were determined by enzyme-linked immunosorbent assay. None of the genotyped SNPs nor EGF-EGFR genotype interactions were associated with RE, BE, or EAC development (p > 0.05 ). Moreover, mRNA expression of neither EGF nor EGFR differed between samples of the esophageal tissue with and without endoscopically visible pathology (p > 0.05 ) nor between samples from patients with different diagnoses, i.e., RE, BE, or EAC (p > 0.05 ). Nevertheless, the lower EGF mRNA expression in carriers of combined genotypes AA +61 EGF (rs4444903) and GG +142285 EGFR (rs2227983; p < 0.05 ) suggests a possible direct/indirect effect of EGF - EGFR gene interactions on EGF gene expression. In conclusion, EGF and EGFR gene variants and their mRNA/protein expression were not associated with RE, BE or EAC development in the Central European population.