Lack of Association between Epidermal Growth Factor or Its Receptor and Reflux Esophagitis, Barrett’s Esophagus, and Esophageal Adenocarcinoma: A Case-Control Study

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

doi:https://doi.org/10.1155/2022/8790748

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Research Article | Open Access

Volume 2022 | Article ID 8790748 | https://doi.org/10.1155/2022/8790748

Lack of Association between Epidermal Growth Factor or Its Receptor and Reflux Esophagitis, Barrett’s Esophagus, and Esophageal Adenocarcinoma: A Case-Control Study

Tereza Deissova,^1,2Michaela Cvanova,^1,3Zdenek Kala,⁴Zuzana Jiraskova Zakostelska,⁵Jiri Dolina,⁶Lumir Kunovsky,^4,7,8Radek Kroupa,⁶Zdenek Pavlovsky,⁹Bretislav Lipovy,¹⁰Zdenek Danek,^1,11Lydie Izakovicova Holla,^2,12and Ondrej Urban⁷ et al.

Academic Editor: Michele Malaguarnera

Received25 May 2022

Accepted03 Aug 2022

Published31 Aug 2022

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 (). Moreover, mRNA expression of neither EGF nor EGFR differed between samples of the esophageal tissue with and without endoscopically visible pathology () nor between samples from patients with different diagnoses, i.e., RE, BE, or EAC (). Nevertheless, the lower EGF mRNA expression in carriers of combined genotypes AA +61 EGF (rs4444903) and GG +142285 EGFR (rs2227983; ) 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.

1. Introduction

Gastroesophageal reflux disease (GERD) is a common gastrointestinal illness developing when the reflux of gastric contents into the esophagus causes symptoms and/or complications—reflux esophagitis (RE), Barrett’s esophagus (BE), and esophageal adenocarcinoma (EAC) [1, 2]. Patients with typical symptoms but no endoscopically visible esophageal mucosal injury are diagnosed with nonerosive reflux disease (NERD). Macroscopic mucosal lesions are visible in the RE, BE, and EAC. The progression from NERD to more severe forms of the disease or to GERD is uncommon [3, 4].

The epidermal growth factor (EGF) and its receptor (EGFR) signaling pathway plays an essential role not only during physiological maintenance of the epithelium (oral, nasal, esophageal, gastric, and intestinal mucosa) but also in numerous pathological processes (mucosal ulcers, inflammatory bowel diseases, etc.) [5–9]. A number of EGFR ligands cause allosteric changes in the intracellular domain of this transmembrane receptor and activation of tyrosine kinase [10]; of this receptor’s ligands, the transforming growth factor α (TGFα) appears to play the most important role in the healing of acute mucosal defects, while EGF is predominantly involved in the healing of chronic ulcerations [6, 11, 12]. The biological function of the EGF/EGFR signaling pathway lies, in particular, in cell proliferation, migration, adhesion, and differentiation, as well as in the inhibition of gastric acid secretion (stimulation of the Na⁺/H⁺ exchanger) and in the protection of the mucosa from chemical, physical, and biological stresses [5, 13–15].

The effects of EGF on the healing of gastric or duodenal mucosa were demonstrated in vivo in rabbits and rats [16–19]. EGF is produced in many parts of the gastrointestinal tract (GIT), including salivary glands, pancreas, and Brunner’s glands of the proximal duodenum. In addition, the application of exogenous EGF was shown to significantly increase the rate of wound healing in an EGFR-dependent manner in an in vitro model of vocal folds wound healing [20]. In addition, the inactivation of EGFR by deoxycholic acid activated an intestine-specific cascade typical for Barrett’s metaplasia. Therefore, active EGFR signaling pathway may play a protective role in BE development [20, 21]. Conversely, the loss of this intestinal program and overactivation of EGFR lead to uncontrolled growth and progression from metaplasia to carcinoma [20, 22]. Moreover, in the process of premalignant progression of BE, the dysplastic BE cells and normal epithelial cells around them exhibit marked downregulation of the EGFR signaling pathway, which prevents neoplastic transformation [23].

A functional polymorphism has been found in the EGFR gene; the variant +142285 G>A EGFR (rs2227983) is characterized by the amino acid substitution of arginine for lysine in the extracellular domain of the receptor and affects the affinity of EGFR ligands (EGF, TGFα), increases its tyrosine kinase activity, attenuates growth stimulation, and decreases the induction of protooncogenes Fos, Jun, and Myc [24]. Also, the expression of EGF could be affected by the +61 EGF A>G (rs4444903) functional polymorphism located in the 5 untranslated (promoter) region of the EGF gene (see Figure 1) [25]. The G allele of +61 EGF A>G (rs4444903) polymorphism was associated with higher EGF serum levels in patients with GERD [26]. Moreover, the EGF-EGFR gene-gene interaction was shown to increase the susceptibility to esophageal cancer [27].

Based on previous findings in different populations [25–29], we aimed to find out if the variability in EGF and EGFR genes, their interaction, and expression constitute risk factors or disease markers of RE/BE/EAC development and progression in the Central European population. To this date, there is no study focused on EGF/EGFR gene variability in the European Caucasian population, and the findings from others cannot be reliably applied to this population due to interpopulational genetic differences. The presented study aimed to (1) analyze the two functional single-nucleotide polymorphisms (SNPs) in the EGF and EGFR genes and their gene-gene interactions in relation to the development of BE and EAC, (2) analyze EGF and EGFR mRNA expressions in the esophageal tissue samples with and without endoscopically visible pathological changes in GERD patients, and (3) compare EGF plasma levels in patients with GERD to those found in healthy controls from the Central European population.

2. Materials and Methods

2.1. Study Design, Inclusion and Exclusion Criteria, and Clinical and Histopathological Examination

The study was approved by the Ethics Committees of the Faculty of Medicine, Masaryk University (No. 09/2020, March 11^th, 2020), University Hospital Brno (No. 01-290605/EK, June 29^th, 2005, No. 05-101019/EK, May 15^th, 2019), University Hospital Motol, Prague (without number, June 19^th, 2019), and University Hospital Olomouc (No. 104/19, June 25^th, 2019).

Written informed consent was obtained from all participants, in line with the Helsinki declaration, before inclusion in the study. In this study, a total of 407 individuals from the Czech and Slovak populations were enrolled. Subjects were examined at the Department of Gastroenterology, University Hospital Brno, Czech Republic, 3rd Department of Surgery, University Hospital Motol, Prague, Czech Republic, and Department of Gastroenterology and Geriatrics, University Hospital Olomouc, Czech Republic, between 2005 and 2021. Inclusion criteria were as follows: , willingness to participate in the study and to sign the informed consent, and willingness to undergo endoscopic examination. Exclusion criteria were as follows: close family relationship to another participant in the study, other than Caucasian race, hepatic/renal failure, other types of tumors, and pregnancy.

All participants underwent esophagogastroduodenoscopy (EGD) with standard indications (patients with dyspepsia, dysphagia, epigastric pain, heartburn, regurgitation, anemia, etc.) and/or for this study purposes (individuals without digestive disease). During EGD, the duodenum, stomach, and esophagus were examined and biopsy samples taken. Patients were diagnosed endoscopically according to the Savary-Miller (SM) classification or Los Angeles classification; also, Barrett’s C/M Prague criteria were used. BE was defined according to the European Society of Gastrointestinal Endoscopy guidelines [30]; EAC was confirmed by histological examination.

In this case-control association study, participants were divided into two groups according to their clinical diagnosis. Group 1 consisted of patients with endoscopically confirmed esophageal injury and/or complications related to GERD (RE, BE, and EAC). Patients with GERD-related symptoms but without visible pathology on endoscopy (NERD) and healthy individuals with respect to inclusion and exclusion criteria were included in Group 2. The flowchart of performed analyses is in the Supplementary Material (Figure S1).

2.2. Samples Collection, DNA, and RNA Isolation

From each subject, 9 mL of peripheral blood was collected into a tube containing 0.5 M EDTA (S-Monovette® 9 mL K3E, Sarstedt, Germany). Plasma was separated from these samples by centrifugation (2000 g, 4°C, 10 min) within 60 minutes of collection, aliquoted (), and stored at −70°C until ELISA analysis. The remaining plasma was used for DNA isolation from leukocytes based on the modified salting-out method with proteinase K digestion of cells [31].

The biopsies from 23 patients with RE, BE, or EAC were collected only at the Department of Gastroenterology, University Hospital Brno, Czech Republic. Four biopsies were taken from each patient’s esophagus during the endoscopic examination of the upper GIT. Two samples were collected from the part with endoscopically visible pathological changes and two from the part without such apparent changes. In this way, we acquired two pairs of samples, each pair containing one sample from the seemingly pathological and one from the seemingly healthy tissue. One pair was placed into 1.8 mL cryovials (SPL Life Sciences, Korea) with 1 mL of RNAlater™ Stabilization Solution (Thermo Fisher Scientific, Waltham, MA, USA) and stored at −70°C until RNA extraction. The other pair was sent to the Department of Pathology, Faculty Hospital Brno, Czech Republic, for histopathological confirmation of the diagnosis.

2.3. Genotyping of Polymorphisms in EGF and EGFR

This genetic association study comprised the entire study population () and was designed as a case-control study. Genotyping of two functional SNPs +61 A>G EGF (rs4444903) and +142285 G>A EGFR (rs2227983) was performed by qPCR using nuclease TaqMan™ SNP Genotyping Assays (C__27031637_30 and C__16170352_20, respectively). The reaction mixture was prepared and conditions set in accordance with the manufacturer’s instructions (Thermo Fisher Scientific, Waltham, MA, USA); fluorescence was measured using the Roche LightCycler® 96 System (Roche, Mannheim, Germany) at the Department of Pathophysiology, Faculty of Medicine, Masaryk University, Brno, Czech Republic. The LightCycler® 96 Application Software was used to analyze real-time and endpoint fluorescence data. Genotyping was verified by using positive control subjects in each 96-well plate and % of the samples, which were 100% concordant. The gene-gene interaction analysis was based on the method used by Upadhyay et al. [27] who modeled the combination of the genotypes bearing risk for GERD development, namely, +61 AA EGF (rs4444903) and+142285 GG EGFR (rs2227983).

2.4. Analysis of EGF and EGFR Gene Expressions

The relative quantifications of EGF and EGFR mRNA were performed in esophageal tissues with/without endoscopically visible pathological changes in 23 patients with GERD; namely, these comprised 10 patients with RE, 6 with BE, and 7 with EAC. Total RNA was isolated from fresh biopsies using AllPrep DNA/RNA/miRNA Universal Kit (Qiagen, Hilden, Germany). Firstly, the RNAlater™ Stabilization Solution (Thermo Fisher Scientific, Waltham, MA, USA) was removed. Subsequently, the tissues were homogenized s at 6500 RPM in 600 μL lysis buffer with 2 g of Ceramic Beads, 1.4 mm (Qiagen, Hilden, Germany) using Precellys® Evolution homogenizer (Bertin Technologies SAS, France). Isolated total RNA was quantified using the NanoDrop 2000c spectrophotometer (Thermo Fisher Scientific, Waltham, MA, USA) and stored at −70°C until use. The cDNA was transcripted using the Transcriptor first strand cDNA synthesis kit with a mix of random hexamer primers and an anchored-oligo(dT)18 primer. The reaction mixture and conditions were designed according to the manufacturer’s instructions (Roche, Mannheim, Germany). Expression of target EGF or EGFR genes and housekeeping gene glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was analyzed using the TaqMan™ Gene Expression Assays (Hs01099990_m1, Hs01076090_m1, and Hs02758991_g1). The manufacturer’s procedure was followed (Thermo Fisher Scientific, Waltham, MA, USA), and fluorescence was measured using Roche LightCycler® 480 System (Roche, Mannheim, Germany) at the Department of Biochemistry, Faculty of Science, Masaryk University, Brno, Czech Republic. All reactions were performed in triplicates. The LightCycler® 480 Application Software was used to analyze the cycle threshold (Ct) values for relative gene quantification.

2.5. Analysis of EGF Plasma Levels

Plasma EGF levels were measured in 8 healthy individuals from Group 2 (healthy controls, HC) and 29 patients with GERD from Group 1 using the commercially available Human EGF, DuoSet® ELISA kit (Bio-Techne R&D Systems s.r.o., UK); namely, the 29 patients with GERD included 10 patients with RE, 9 with BE, and 10 with EAC, respectively. All tests were performed according to the manufacturers’ recommendations.

2.6. Statistical Analysis

All statistical analyses were performed using the program IBM SPSS Statistics for Windows, version 26. The age distribution of the patients among groups was compared by Kruskal-Wallis or Mann–Whitney test. The genotype and allele frequencies, Hardy–Weinberg equilibrium (HWE), and differences in sex representation were tested using the Pearson test. As the patients differed in age and sex in the genetic association study, the results were adjusted for these parameters to be able to compare our results with those of the study by Upadhyay et al. [27] who also presented adjusted results. The results are supplemented with odds ratios (OR) and 95% confidence intervals (CI) from logistic regression analysis, where OR are related to all other genotypes. In the case of gene-gene interaction analysis, the ORs are related to the reference group. The reference genotype was established according to Upadhyay et al. [27] and compared with the rest of the genotypes in the group of GERD patients by logistic regression.

The variation in mRNA expressions in tissues with and without endoscopically visible pathological changes was evaluated using Wilcoxon signed ranked test. Kruskal-Wallis or Mann–Whitney tests were used to test the expression differences in tissues with and without endoscopically visible pathological changes in the groups of patients according to their diagnosis or studied polymorphism. The Kruskal-Wallis or Mann–Whitney tests were also performed to compare plasma concentrations among the groups. Graphs were created in the software OriginPro, Version 2021b (OriginLab Corporation, Northampton, MA, USA).

3. Results

3.1. Demographic Data of the Studied Population

The investigated population included 161 patients with RE, 92 with BE, and 48 with EAC, constituting Group 1 (). The 8 healthy individuals and 98 patients with NERD were included in Group 2. The demographic data are given for each analysis separately (see Table 1). Significant differences were found in the age distribution across groups in the populations used for the genetic association study () and for the analysis of plasmatic EGF protein levels (, see Table 1). A post hoc analysis revealed that all pairs of groups in the genetic association study also differed significantly in age, except for the NERD vs RE (; data not shown); in the study of EGF plasma levels, none of the age differences in the individual groups were significant, with the exception of Group 2 (that consisted only of healthy individuals; median age 35.0) and patients with EAC (median age 68.0; ; data not shown). The representation of men in the population used for the genetic association study was higher in Group 1 and its subgroups (RE, BE, EAC) than in Group 2 (; see Table 1). Where EGF/EGFR mRNA expression and EGF plasma levels analyses were concerned, the presence of men was similar among subgroups (; see Table 1).

3.2. Genetic Association Case-Control Study

A total of 407 individuals, including 301 patients with GERD and 106 persons in Group 2 (98 patients with NERD and 8 healthy control), were genotyped for +61 A>G EGF (rs4444903) and +142285 G>A EGFR (rs2227983) polymorphisms. The allele and genotype frequencies of neither of the two polymorphisms, adjusted for age and sex, differed between Group 1 and Group 2, even when comparing Group 2 to subgroups according to the specific diagnoses of RE, BE, or EAC, respectively (; see Table 2). Unadjusted data are shown in the Supplementary Material (Table S1).

In addition, none of the EGF-EGFR genotypes interactions showed effects on the risk of developing GERD or its complications in comparison with reference genotypes EGF-EGFR AG-AA, AG-AG, GG-AA, and GG-AG (; see Tables 3–4), adjusted for age and sex. Unadjusted data are shown in the Supplementary Material (Tables S2–S3).

3.3. Expression of EGF and EGFR Genes in the Esophageal Tissue

The expressions of EGF/EGFR mRNA were, according to delta-Ct values, similar in the esophageal tissues with/without endoscopically visible pathological changes in patients with GERD (; ; data not shown). No differences in EGF/EGFR mRNA expressions were revealed among the RE, BE, and EAC tissue biopsies using the delta-delta Ct method, either (; Figure 2).

3.4. EGF Protein Levels in Plasma

Plasma levels of EGF did not significantly differ between patients with complications of GERD (RE, BE, or EAC) and healthy controls (HC; p >0.05; see Figure 3).

3.5. Relations between +61 A>G EGF (rs4444903) and +142285 EGFR G>A (rs2227983) Polymorphisms, EGF Plasma Levels, and EGF and EGFR mRNA Expressions in Esophageal Tissue

Our results showed that the polymorphism +61 A>G EGF (rs4444903) did not affect EGF plasma levels either in patients with GERD () or in healthy controls (; ; data not shown).

Relationships between genotypes and mRNA expressions were analyzed using the delta-delta Ct method. The EGF or EGFR mRNA expressions in esophageal tissue of GERD patients () were independent on +61 A>G EGF (rs4444903) or +142285 G>A EGFR (rs2227983) polymorphisms (; data not shown).

However, the EGF mRNA expression was significantly lower in GERD patients with the genotype combination AA-GG (EGF-EGFR; , of which ) than in carriers of any other combination (; logistic regression: , OR: 3.15, see Figure 4).

4. Discussion

In our case-control study, we focused on a complex EGF/EGFR analysis in groups of patients with (Group 1) and without (Group 2) esophageal mucosal damage.

4.1. Genetic Association Case-Control Study

At first, we examined the functional +61 EGF A>G (rs4444903) and +142285 G>A EGFR (rs2227983) polymorphisms in GERD patients. These SNPs were analyzed by previous studies with controversial results. Lurje et al. associated the genotype AA of +61 EGF A>G (rs4444903) polymorphism with a higher likelihood of developing EAC recurrence [28]. Conversely, Lanuti et al. and Cheung et al. associated the presence of genotypes AG or GG of +61 EGF A>G (rs4444903) with an increased risk of EAC development in patients with GERD [26, 29]. In the case of the +142285 G>A EGFR (rs2227983) polymorphism, Yang et al. associated the allele A (phenotype with low activity of EGFR) with the risk of death and squamous cell carcinoma (ESCC) recurrence [32]. In addition, the EGF-EGFR interaction, especially the genotypes AA +61 EGF A>G (rs4444903; phenotype with low expression of EGF) and GG +142285 G>A EGFR (rs2227983), were shown to increase (2.5-fold) the susceptibility to esophageal cancer in a group of 159 patients with ESCC and 15 patients with EAC in comparison with a group of 196 endoscopically unexamined controls from the Indian population [27].

In our study, the +61 EGF A>G (rs4444903) and +142285 G>A EGFR (rs2227983) polymorphisms or their EGF-EGFR genotype interaction was not associated with the increased risk of GERD or its complications. In contrast to the study by Upadhyay et al. [27], our analysis was performed in 48 patients with EAC only vs. 106 endoscopically examined patients without inflammation or tissue changes in esophageal mucosa. The difference in results may be also affected by the interpopulational variability. According to NCBI, the minor allele frequencies (MAF) of +61 EGF A>G (rs4444903) and +142285 G>A EGFR (rs2227983) polymorphisms were 39.1% (allele G; rs4444903) and 27.6% (allele A; rs2227983), respectively, in the European (EUR) population compared with 54.1% (allele G; rs4444903) and 35.1% (allele A; rs2227983), respectively, in the South Asian (SAS) population. The MAFs in our “control” group corresponded to the EUR population (NCBI, ); specifically, the allele G of EGF rs4444903 was present in 41% (; ) of participants and the allele A of EGFR rs2227983 was carried by 24.5% (; ) of participants in our study. In addition, we analyzed not only distributions of studied polymorphisms, but also EGF/EGFR mRNA expression and EGF plasma level that were considered together with EGF-EGFR gene-gene interaction.

The main advantage of our study, compared with all others [25–29], lies in the fact that ours is the only one in which the control group consists of individuals with endoscopically and histopathologically examined esophagus. Limitations of our genetic association case-control study include the statistically significant differences in age and sex distributions across studied groups. These differences in our cohort were, nevertheless, expected because GERD progression is age-related [32, 33], and men are known to suffer from RE, BE, and EAC more frequently than women [34]. To eliminate this possible bias, the data were adjusted for both these parameters.

4.2. EGF/EGFR mRNA Expression Analysis

Even though it was reported that 90% of esophageal cancer show EGFR upregulation [35] and a recent meta-analysis found EGFR overexpression to be a predictive biomarker in clinical practice (because of its correlation with the clinicopathological features and overall survival prognostic value [36]), our study revealed no differences in EGF and EGFR mRNA expressions in esophageal tissues with or without endoscopically visible pathological changes in GERD patients. Moreover, we did not observe any changes in the EGF or EGFR mRNA expressions with the severity of the disease (RE, BE, or EAC).

Our results are consistent with the findings of a prospective study by Vallböhmer et al. who found no difference between EGFR mRNA expression in 59 patients with BE, dysplasia, or EAC (case group) and 16 patients with normal esophageal pH and no histological evidence of mucosal injury (control group). No correlation between EGFR mRNA expression and disease progression was detected in that study, either [37]. In addition, our results are in agreement with those recently reported by Wasielica-Berger et al. who found no significant changes in EGF or EGFR expression (examined by immunohistochemistry) in patients with erosive esophagitis compared to NERD patients. However, they revealed a positive correlation between EGFR expression and the presence of basal cell hyperplasia [38]. On the other hand, EGFR levels do not correlate with the EGFR signaling pathway activity that is mediated by an activation mutation or ligand binding. Baal et al. detected lower expression of phosphorylated (active) EGFR in BE tissues compared to the squamous esophageal tissue in the same patients (age range 44–86 years) [39]. However, it must be taken into account that the increased activation of EGFR could be associated with aging (as found in rats) [40]. In our EGF/EGFR expression analysis, the age and sex distributions were similar among subgroups (RE, BE, and EAC). The greatest strength of the presented study lies in the investigation of the EGF/EGFR expression in both types of tissues in the same GERD patients, which eliminates the effect of biological variability. Nevertheless, due to the relatively small number of patients, which remains a limitation of this part of the study, the results are rather indicative and should be verified in a larger cohort.

4.3. EGF Plasma Level Analysis

Finally, we analyzed the EGF plasma levels in patients with GERD. Benamouzig et al. did not find any association between the presence of RE with either EGFR expression or serum (or salivary) EGF levels [41]. In line with these findings, the EGF plasma levels were not associated with RE, BE, or with EAC in our patients. It seems more appropriate to study EGF levels in plasma than in the serum because, unlike EGF serum levels, EGF plasma levels are not correlated with the platelet count [42]. Also, in this case, it must be considered that the EGF blood levels change even naturally with age and sex. For example, the levels of EGF in platelet-rich plasma were shown to be higher in women than in men and in individuals younger than 26 years than in older ones, respectively [43]. EGF levels inversely correlate with age in healthy individuals [44]. In this part of our study, the sex distribution was similar among studied subgroups; however, the fact that the age was significantly different between Group 2 (consisting only of healthy individuals) and patients with EAC can be considered a limitation of this study.

4.4. Relations between +61 A>G EGF (rs4444903) and +142285 EGFR G>A (rs2227983) Polymorphisms and EGF/EGFR mRNA Expressions or EGF Plasma Levels

EGF/EGFR gene expression can be, besides transcription factors [45], miRNAs [46], hormones [47], and epigenetic modifications [48], also regulated by gene mutations. We assumed that the studied functional polymorphisms could influence EGF/EGFR production and, thus, contribute to disease progression. Lanuti et al. found out that the genotype GG of +61 EGF A>G (rs4444903) was significantly more common among the 312 patients with EAC than among 447 controls without a history of GERD (self-reported), in a mostly Caucasian population (98%). In addition, this GG genotype was associated with higher EGF serum levels in 82 patients with BE but not in those with GERD without endoscopically visible mucosal esophageal damages () [26]. Unfortunately, it is not clear whether the higher EGF serum levels are associated with the presence of the GG genotype or with the presence of BE. Menke et al. reported a significantly increased frequency of the GG genotype of this SNP in patients with RE (), BE (), and EAC () in comparison with endoscopically unexamined controls () in a mostly Caucasian population. Moreover, the lower local EGF, investigated by immunohistochemical methods, was associated with carriage allele G of +61 EGF A>G (rs4444903) in 37 BE biopsies. Menke et al. suggested that the decreased EGF protein level in BE biopsies may support esophageal tumor development by reducing mucosal protection [49]. However, it is necessary to bear in mind that they examined the +61 EGF A>G (rs4444903) germinal variant in the genomic DNA from the samples of whole blood, not from BE biopsies, and the genotype in the affected tissue may differ from that observed in the whole blood.

In our study, the EGF mRNA expression in esophageal tissues or EGF plasma level was independent of the +61 EGF A>G (rs4444903) polymorphism. Similarly, the polymorphism +142285 G>A EGFR (rs2227983) was not associated with mRNA EGFR expression in the esophageal tissue of GERD patients. In contrast to a previous study using formalin-fixed, paraffin-embedded esophageal tissues, and immunohistochemistry for analysis of the EGF protein levels, we examined EGF mRNA expression in fresh esophageal tissues by RT-qPCR in our study. Moreover, we investigated EGF mRNA expression in both pathological and endoscopically normal esophageal tissues from the same patients to eliminate the biological variability. This could be one of the possible explanations for the observed differences in results. However, we found a significantly lower EGF mRNA expression in GERD patients with the combined AA-GG genotype (EGF-EGFR) that Upadhyay et al. [27] associated with the increasing risk of esophageal cancer. Our finding is in line with the study by Shahbazi et al. [25], where mononuclear cells from the peripheral blood of individuals with the AA genotype of +61 EGF A>G (rs4444903) produced significantly less EGF mRNA than the cells from the GG genotype carriers or heterozygous individuals. Also, Suenaga et al. associated the genotype AA of this SNP with lower tumoral EGF mRNA expression in Japanese patients with hepatocellular carcinoma [50]. It is possible that EGF expression can be directly or indirectly influenced by EGF-EGFR gene interaction. This relationship has not been described; hence, further analyses are needed for verification and explanation of these results on a larger sample.

5. Conclusions

The literature suggests that the EGF/EGFR signaling pathway plays a pleiotropic role in GERD development. While the active EGF/EGFR signaling pathway prevents the transformation of the normal esophageal squamous cell epithelium to BE, it also contributes to the malignant progression of BE. In our complex case-control study analysis, we have shown that neither (i) the +61 EGF A>G (rs4444903) and +142285 G>A EGFR (rs2227983) polymorphisms nor (ii) mRNA EGF or EGFR expressions and (iii) EGF plasma levels can be used as markers for the RE, BE, and EAC in the Central European population. In conclusion, our results show that the role of EGF/EGFR, especially functional gene variants, in BE and EAC development is not as important as we hypothesized.

However, the combination of genotypes AA-GG (EGF-EGFR) was associated with lower EGF mRNA expression; hence, the EGF mRNA expression may be directly or indirectly affected by the interaction of these genes.

Data Availability

The analyzed data used in this study are available from the corresponding author and the first author (raw data) upon request.

Disclosure

The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results. This publication reflects only the author’s view, and the European Commission is not responsible for any use that may be made of the information it contains.

Conflicts of Interest

The authors declare no conflict of interest.

Authors’ Contributions

TD contributed to the design of the study, data interpretation, carried out the genotyping and analysis of mRNA, created the figure, and drafted the paper. MC performed the statistical analysis and created the presentation of results. ZK supervised the clinical part of the study and critically reviewed the manuscript. ZJZ designed and carried out the analysis of EGF plasma levels and critically reviewed the manuscript. JD participated in the clinical part of the study and was responsible for the clinical examination and sample collection. LK participated in the clinical part of the study and was responsible for the clinical examination and sample collection. RK participated in the clinical part of the study and was responsible for the clinical examination and sample collection. TH cosupervised the clinical part of the study, provided the clinical part of the study, and was responsible for the clinical examination and sample collection. OU cosupervised the clinical part of the study, provided the clinical part of the study, and was responsible for the clinical examination and sample collection. ZP carried out the histopathological examination. BL drafted the paper. ZD contributed to the data interpretation and critically reviewed the manuscript. LIH performed the statistical analysis in the pilot study and critically reviewed the manuscript. OU supervised the clinical part of the study and critically reviewed the manuscript. VN participated in the clinical part of the study and was responsible for the clinical examination and sample collection. RL supervised the clinical part of the study and critically reviewed the manuscript. TH participated in the clinical part of the study and was responsible for the clinical examination and sample collection. TG participated in the clinical part of the study and was responsible for the clinical examination and sample collection. VP participated in the clinical part of the study and was responsible for the clinical examination and sample collection. OS critically reviewed the manuscript. PBL designed the study, interpreted data, suggested presentation of results, and drafted the paper. All authors revised the final version of the manuscript.

Acknowledgments

This study was supported by the Ministry of Health of the Czech Republic (grant no. NU20-03-00126) and by the Ministry of Health of the Czech Republic-conceptual development of research organization (FNBr, 65269705, Sup 3/21). This publication has received funding from the European Union’s Horizon 2020 Research and Innovation Programme under grant agreement No. 857560. The authors also thank Research Infrastructure RECETOX RI (No. LM2018121) and project CETOCOEN EXCELLENCE (No. CZ.02.1.01/0.0/0.0/17_043/0009632) financed by the Ministry of Education, Youth and Sports for supportive background. This study was supported by the Ministry of Health of the Czech Republic, grant no. NPV II 2B06060. We would like to thank Dr. Jaroslav Janošek for his valuable comments

Supplementary Materials

Supplementary 1. Figure S1: the flowchart of analyses performed in this study.

Supplementary 2. Table S1: allele and genotype frequencies of the +61 A>G EGF (rs4444903) and +142285 G>A EGFR (rs2227983) polymorphisms in study groups ().

Supplementary 3. Table S2: gene-gene interaction: +61 A>G EGF (rs4444903) and +142285 G>A EGFR (rs2227983) between study groups ().

Supplementary 4. Table S3: gene-gene interaction: +61 A>G EGF (rs4444903) and +142285 G>A EGFR (rs2227983) between the NERD patients and individual subgroups with RE/BE/EAC ().

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