- Research Article
- Open Access
Prevalence and characteristics of Epstein–Barr virus-associated gastric carcinomas in Portugal
Infectious Agents and Cancer volume 12, Article number: 41 (2017)
Gastric cancer (GC) is one of the most common malignant tumors of the digestive tract and is the third leading cause of cancer death worldwide. Epstein–Barr virus (EBV) has been associated with approximately 10% of the total cases of gastric carcinomas. No previous study has analyzed the prevalence of EBV infection in gastric cancer of the Portuguese population.
In the present study, we have analyzed 82 gastric carcinoma cases and 33 healthy individuals (control group) from Coimbra region for the presence of EBV by polymerase chain reaction (PCR) and by in situ hybridization (ISH) for EBV-encoded small RNAs (EBERs). The status of H. pylori infection was assessed by serology and by PCR.
EBV was detected by PCR in 90.2% of stomach cancer cases, whereas EBERs were detected in 11%. In our series, EBV-associated gastric carcinoma (EBVaGC) were significantly associated with gender and the majority of them presented lymph node metastasis. These cases were generally graded in more advanced pTNM stages and, non-surprisingly, showed worse survival. H. pylori infection was detected in 62.2% of the gastric cancers and 64.7% of these patients were CagA+. On the other hand, the H. pylori prevalence was higher in the EBV-negative gastric carcinomas (64.4%) than in those carcinoma cases with EBV+ (44.4%).
The present study shows that prevalence of EBVaGC among Portuguese population is in accordance with the worldwide prevalence. EBV infection seems to be associated to poorer prognostic and no relation to H. pylori infection has been found. Conversely, the presence of H. pylori seems to have a favourable impact on patient’s survival. Our results emphasize that geographic variation can contribute with new epidemiological data on the association of EBV with gastric cancer.
Gastric cancer (GC) is one of the most frequent malignant tumors of the digestive tract and is the fifth most commonly diagnosed cancer and the third leading cause of cancer death worldwide (723,073 deaths, 8.8% of the total) . As so, associations to other comorbidities, such as the Epstein-Barr virus and the Helicobacter pylori infection, are extremely important as they may be used either clinically as prognosis factor or in basic research to get a deeper understanding of the underlying mechanisms.
The Epstein-Barr virus (EBV) belongs to the Herpesviridae family and approximately 95% of the world’s population is infected with it, being the oral route the principal way of infection . In 1997, the International Agency for Research on Cancer (IARC) has classified EBV as a Group I carcinogen for Burkitt’s lymphoma, nasopharyngeal carcinoma and for Hodgkin’s and non- Hodgkin’s lymphoma .
The presence of EBV in a patient with gastric cancer was first reported in a case of lymphoepithelioma type by Burke et al. in 1990 . Subsequently, Shibata and Weiss have identified the presence of EBV in 16% of gastric adenocarcinomas in USA .Unlike other EBV-associated malignancies, the EBV-associated gastric carcinoma (EBVaGC) is not endemic in any region yet is quite distributed worldwide. In fact, it is emerging as the most common among EBV-associated malignant neoplasms with more than 90,000 patients being estimated to develop GC in association with EBV annually (10% of total GC) [6,7,8].
H. pylori is the major causative agent of gastritis, peptic ulcer disease, mucosa-associated lymphoid tissue (MALT) lymphoma, and GC .The clinical outcome of H. pylori infection depends on bacterial virulence factors, host susceptibility, environmental and life-style factors . Several H. pylori virulence genes have also been identified and among those cagA (cytotoxin-associated gene) is one of the most important gene. Infection with CagA strains is associated to higher risk of developing atrophic gastritis and gastric cancer [11, 12].
Some studies have addressed the question if exists a cooperative effect between EBV and H. pylori in GC but, their results are inconsistent and conflicting. The present study aims at determining the frequency of EBV-related gastric carcinoma in the Portuguese population and drawing both epidemiological and clinicopathological features of EBV-associated GC in this geographic area relating to H. pylori infection.
Patients and samples
A total of 82 patients with gastric cancer who underwent surgical resection at Coimbra University Hospital (HUC) and Regional Oncology Center of Coimbra, IPOFG, SA and 33 patients with non-cancer diseases (control group) who underwent routine surveillance endoscopy at Gastroenterology department of HUC by nonspecific complaints were enrolled in our study. Serum, tumor tissue and their corresponding adjacent non-cancerous mucosa was collected from each gastric cancer patient. Gastric tissue samples and serum were obtained from each individual of the control group.
This study was approved by Ethics Committee of the respective institutions and informed consent was obtained from all individuals. None of the patients received chemotherapy or radiation therapy before surgery. Patient overall survival times were calculated from the date of diagnosis to either the date of death or the last follow up, resulting in a follow-up period ranging from 1 to 55 months (mean, 36 months). Those cases lost to follow-up and those ending in death from any other cause than gastric cancer (2 cases) were considered censored data during the analysis of survival rates.
Clinicopathologic data comprise patient age and gender as well as the anatomical site, histological classification according to the Lauren classification system , and pathological tumor stage (TNM stage; T: depth of tumor invasion, N: lymph node metastasis, M: distant metastasis) according to the American Joint Committee on Cancer (AJCC) system .
DNA from tumor tissue and from non-cancerous mucosa was extracted and purified in MagNA Pure Compact equipment (Roche, Germany) using MagNA Pure Compact Nucleic Acid Isolation Kit I (Roche, Germany), according to manufacturer’s instructions. Prior to extraction on the MagNA Pure Compact, tissues were disrupted in Magna Lyser (Roche, Germany) and treated with ATL buffer (QIAGEN, Spain) and proteinase K (QIAGEN, Spain) for 10 min at 65 °C. DNA concentration (A260) and purity (A260/A280) were determined spectrophotometrically (NanoDrop, Thermo Fisher Scientific). DNA was stored at −80 °C for further use.
EBV real-time PCR
EBV detection was performed using specific primers described by Drouet et al. (1999)  that amplify a segment of the BamH1W region.
Real-time PCR reactions were carried out on the SmartCycler instrument (Cepheid, USA) in a final volume of 20 μl, containing 2 μl of extracted DNA, 2 μl of FastStart SYBR Green Master kit (Roche, Germany) and 0.4 mM of each primer. Thermocycling conditions were a preheating step of 10 min at 95 °C followed by 45 cycles of 95 °C for 10 s, 59 °C for 5 s and 72 °C for 8 s. Fluorescence was measured at the end of each extension step. Melting analysis was achieved with continuous monitoring of fluorescence from 65 °C to 95 °C at a temperature transition rate of 0.2 °C. A specimen was considered positive if a single melting peak was measured between 88 °C and 89 °C. To validate the amplification process and exclude carryover contamination, positive and negative controls were included in each PCR run.
EBER1 in situ hybridization
The presence of EBV in gastric cells was identified by the expression of EBV-encode small RNA-1 (EBER1), the most abundant viral product in latently infected cells. In situ hybridization reactions were carried out in an automated system, the BOND -MAX ™ (Leica Microsystems, Wetzlar, Germany) using the staining protocol “ISH protocol A” with an enzymatic pre-treatment with the Bond Enzyme Pre-treatment Kit, according to manufacturer’s instructions. From paraffin-embedded tissues were cut 3 histological sections with 3 μm thick that were mounted on glass slides coated with 3-(aminopropyl) triethoxysilane (Sigma Diagnostics, St. Louis, USA) and used for hybridization with 3 different probes: the EBER Probe, the RNA Positive Control Probe and the RNA Negative Control Probe (Leica Microsystems, Wetzlar, Germany). A sample was considered EBER-1-positive when appeared a dark brown staining in the nuclei of tumor cells, under light microscopy. In each hybridization a positive control, Hodgkin’s lymphoma EBV positive and a negative control, Hodgkin’s lymphoma EBV negative were included. The cases with EBER1 positive signals were classified as EBVaGC group.
PCR amplification of H. pylori and cagA gene
Detection of H. pylori in gastric samples was accomplished by amplification of H. pylori flagella gene. For the H. pylori-positive samples, the presence of the cagA gene was assessed. Single type PCRs were performed with specific primers described elsewhere .
H. pylori serology
IgG antibodies against H. pylori were determined with an enzyme-linked immunosorbent assay (ELISA), using a commercial assay (HELICOBACTER PYLORI ELISA IgG, Vircell, Spain), with a sensitivity of 97% and specificity of 100%; according to the manufacturer’s instructions.
The χ2 test and Fisher’s exact test were used to test associations between categorical variables. Cases within the follow-up period were censored either at the time of death or at the last update of the subject. Survival curves were estimated using the Kaplan-Meier product-limit method, and the differences between the survival curves was tested using the log-rank test. All statistical analyses were performed using the Statistical Package for the Social Sciences, version 19 (SPSS Inc., Chicago, IL, USA), and a p value <0.05 was considered as statistically significant.
Prevalence of EBV positive cases
We evaluated 82 patients (45 males and 37 females; mean age, 66.6; range, 39 to 88 years) with gastric carcinoma and 33 patients (13 males and 20 females; mean age 57.8; range, 30 to 82 years) with non-cancer diseases. Using PCR analysis, EBV DNA was detected in 90.2% of the patients with gastric carcinoma and in 27.3% of the individuals from the control group. However, in situ hybridization showed EBER expression in malignant cells in only 9 patients with gastric cancer (corresponding to 11%) and in one case of the control group (3%). In one of the nine cases EBVaGC, the EBER expression was also detected in non-malignant gastric mucosa. The EBER expression in malignant cells was either uniformly positive or uniformly negative, suggesting that EBV infection may have occurred before malignant transformation and was transmitted to all daughter cells in the neoplastic clone.
Association between EBV status and clinicopathological characteristics
The clinicopathological characteristics of EBVaGC and EBV-negative gastric carcinomas (EBVnGC) patients are summarized in Table 1. Gender ratio (male/female) was 8:1 in EBVaGC and 1.03:1 in EBVnGC, revealing a significant (p = 0.037) association where male shows predominance in EBV positive GC. Although there were no statistically significant differences, EBVaGC were more frequently associated with older age group, notably up to 100% of cases were older than 60 years old versus 75% of EBVnGC.
Regarding tumor localization, a tendency for the antrum was denoted in both groups, 55.6% in EBVaGC and 74% in EBVnGC; nonetheless, the percentage of tumors at proximal locations was higher in EBVaGC (44.4% vs. 26%). Tumor histology was not related to EBV status since in both groups intestinal type was predominant. Furthermore, the positivity of EBV was not significantly associated with either stage or survival, whilst a slight tendency of EBVaGC having a worse prognosis was noticed. This perception is based on the fact of EBVaGC patients present higher probability of having lymph node metastasis, were typically stratified in more advanced stages and showed poorer survival rates (Fig. 1). Although this trend could be biased by age, gender and the TNM status a deeper analysis reveals that EBV+ subjects tend to present worse survival rate even correcting for that factors. Nonetheless, the attempted statistical models did not present statistical significance for the EBV groups.
Detection and genotyping of H. pylori
The presence of H. pylori DNA was identified in 62.2% (n = 51) of GC patients and in 54.5% (n = 18) of the control group. Comparing the clinicopathological characteristics between the GC H.pylori + against the GC H. pylori– significant differences due to gender, age, tumor location, histological classification, TMN stage and survival rate were not observed (Table 2). The gene cagA was detected in 64.7% (33/51) of the GC cases with H. pylori infection and in 38.9% (7/18) at the control group with H. pylori infection, which highlights a significant association between the H. pylori strains present in tumors to express gene cagA (p = 0.043). In fact, H. pylori strains found in tumors have about 3 times more probability of being CagA+ (OR: IC95% [1.01, 6.66]) than the H. pylori strains detected in gastric tissue of healthy individuals.
Seroprevalence of H. pylori infection reveals higher rates in GC patients when compared to the control group (85.4% vs 57.6%, p = 0.001). The odds ratio of an individual H. pylori seropositive to have gastric cancer is about 4 times higher than an individual seronegative (95% CI: [1.71, 10.82]).
Concerning seroprevalence another relationship was observed, namely the association with clinical stage; the majority of H. pylori seropositive cases were graded in the less advanced tumors stages (I and II) (p = 0.002). The overall survival also follows this trend but with no statistical significance (Log Rank p = 0.201, Breslow p = 0.141), which is not altered if age, gender and stage status is taken into account.
No significant association was observed between the occurrence of H. pylori infection and EBVaGC, since of the nine EBVaGC cases four had H. pylori co-infection (p = 0.288); moreover the positivity of H. pylori in EBVnGC is higher (64.4%) than that found in EBVaGC (44.4%).
Over the past 50 years there has been a decline in gastric cancer (GC) incidence and mortality, however, it still accounts for 6.8% of all malignant tumors .
In Portugal, the WHO data for 2012 indicate that the GC is the fifth most frequent malignancy, with 3018 new cases (1834 men and 1184 women), and the third most lethal cancer, as it was responsible for the death of 2285 Portuguese .
In the present study, we assessed the status of EBV by PCR and ISH and H. pylori infection by PCR and serology in 82 cases of primary gastric carcinomas and in 33 healthy individuals. To the best of our knowledge this is the first report presenting Portuguese casuistry regarding the association of EBV with stomach cancer and, simultaneously correlating the involvement of these two pathogens in gastric carcinogenesis. Using PCR we found that 90.2% of GC were EBV-positive; extremely high positivities of >80% were as well reported in three studies from India [17,18,19], where EBV detection was also accomplished by PCR; this may be due to the high sensitivity of PCR that amplified indiscriminately EBV DNA present in tumor cells and in tumor-infiltrating lymphocytes. To overcome this issue, it was used EBER in situ hybridization, which is the recommended technique for the detection of EBV in human tissue and tumors because of its high sensitivity and specificity to accurate localize the EBV-infected cells . Hence, by ISH the EBV was detected in 11% of our cases, which is consistent with the prevalence of EBVaGC worldwide, since several studies in the literature report that approximately 10% of gastric carcinomas are associated with EBV [6, 8, 21, 22]. EBER expression was mainly restricted to the tumor tissue, as pointed out by others [23,24,25], however we found one EBVaGC case with EBER positivity in the non-neoplastic mucosa and one patient of the control group, with chronic pangastritis, was also EBV+ in epithelial cells. This is in line with the observations of others who detected EBV in precancerous lesions [5, 7, 22, 26]. Despite being quite rare, the EBV infection in non-neoplastic gastric mucosa indicates that EBV enters the gastric epithelium at an early stage of gastric carcinogenesis preceding the clonal growth of EBV-infected cells and subsequently the development to carcinoma.
In our study, we found that patients with EBV-positive tumors are predominantly male (8: 1), as corroborated by the majority of published reports [5, 6, 20, 23, 24, 27, 28]. This highest incidence in men can be attributed to both genetic status and lifestyle factors. Earlier studies indicate that eating salty or spicy foods, frequently drinking coffee and high-temperature drinks, exposure to wood dust and/or iron filings and smoking are risk factors for developing EBVaGC [6, 29].
Concerning histological classification and topographic distribution we found a prevalence of intestinal type and tumors located in the antrum, which is consistent with others studies [5, 26, 30] but in disagreement in what regards the characteristic of EBVaGC [20, 24].
Although it has been proposed that the presence of EBV in gastric cancers is associated with a better prognosis , former reports are inconsistent. Our results point in the direction that the presence of EBV is a marker of poor prognosis since the majority of our cases have lymph node involvement, are grouped in more advanced stages and, as so, have worse survival.
Taken together, these variations between data might be explained by the contribution of local risk factors, such as geographical and environmental aspects, along with the size and features of the cohort.
It is estimated that H. pylori infects half the world population [11, 32, 33] and is responsible for more than 60% of gastric cancer cases [34, 35]. In this series the prevalence of H. pylori for both groups, patients with carcinoma and controls, fall within the described in the literature. In the control group H. pylori detection rates (DNA - 54.6%, seroprevalence - 57.6%), are close to the average of H. pylori infection rate reported worldwide (50%). In GC patients the H. pylori DNA was found in 62.2% of the cases, which is also in agreement with its involvement in more than 60% of the total gastric tumors. On the other hand, the serologic positivity was 85.4% which is in line with the value found in another Portuguese study (85.5%) in patients with stomach cancer . These differences in detection rates may be explained by the spontaneous disappearance of the Helicobacter pylori during malignant transformation of gastric epithelium, perhaps due to lack of nutrients needed by this bacterium; however, the tumor still occurs after the effective eradication of H. pylori; this occurrence has also been described in other studies .
In the current study, statistical comparison between the 2 groups revealed that seropositive H. pylori status is associated to increasing risk of developing gastric cancer [38, 39] and that H. pylori cagA+ strains are more aggressive than H. pylori cagA- strains, being also linked to stomach adenocarcinoma progression [11, 12]. Regarding the prognostic value of H. pylori status we found a significant association between positive H. pylori status and better outcome, since the tumors H. pylori + are stratified in early pTNM stages, as observed by others [40,41,42]. A plausible explanation for this fact is that H. pylori may contribute to a more efficient immune response against the tumor by triggering a type-1 T-helper-cell response , or it was also suggested that Helicobacter pylori antigens mimic the surface molecules of gastric epithelial cells and that would activate a cross-reactivity of autoantibodies against the tumor cells . The involvement of the microsatellite instability is also highlighted, because it has been related with a higher rate of H. pylori infection and a better postoperative survival .
It has been suggested that EBV and H. pylori can be influenced by each other or cooperated together, in a direct or indirect way, in gastric carcinogenesis. In the present study no statistical association was found between EBV infection and H. pylori infection once there is no evidence of an H. pylori co-participation in the 11% of the GCs that are EBV positive by EBER-ISH. In fact, several studies that address the effect and interaction between them do not detected any association [20, 23, 46,47,48,49]. However, there are others publications showing synergism between EBV and H. pylori in the pathogenesis of gastric diseases [30, 50,51,52,53]. In point of fact, it is suggested two possible mechanisms, first an additional inflammatory response in co-infection and increased tissue damaging by both H. pylori and EBV. The studies by Cárdenas-Mondragón et co-workers give evidence of this mechanism; in pediatrics patients they demonstrated that co-infection with EBV and H. pylori CagA+ is more associated with severe gastritis than cases with single H. pylori CagA+ infection , as well as the study with Latin American patients confirm that EBV co-participates with H. pylori to induce severe inflammation and increase the risk of progression to intestinal-type GC . The second mechanism pointed out is based on gene products interaction. An in vitro study found that EBV reactivation occurs by the PLCγ signalling pathway and H. pylori toxin CagA strongly activates PLCγ . On the other hand, Saju et al. suggested that host protein SHP1 dephosphorylates CagA, thus preventing its oncogenic activity; however EBV co-infection causes SHP1 methylation and prevents its dephosphorylation activity of CagA and thereby increasing the oncogenic potential of CagA .
We identified 9 cases of EBVaGC (11%) corresponding to the average prevalence of EBVaGC worldwide. EBVaGC was associated with male predominance and seems to emerge as a factor of poor prognosis, while H. pylori infection appears to have a protective role in the outcome of GC patients. This results highlight that geographic variation can contribute with new epidemiological data on the association of EBV with GC.
American Joint Committee on Cancer
- cagA :
EBV-encoded small RNAs
EBV-associated gastric carcinoma
EBV-negative gastric carcinomas
enzyme-linked immunosorbent assay
Coimbra University Hospital
International Agency for Research on Cancer
In situ hybridization
mucosa-associated lymphoid tissue
polymerase chain reaction
World Health Organization
Ferlay J, Soerjomataram I, Ervik M, Dikshit R, Eser S, Mathers C, et al. GLOBOCAN 2012 v1.0, cancer incidence and mortality worldwide: IARC CancerBase no. 11 [internet]. Lyon, France: International Agency for Research on Cancer; 2013. Available from: http://globocan.iarc.fr. accessed on 20 July 2016
Rickinson AB, Kieff E. Epstein–Barr virus. In: Knipe DM, Howley PM, editors. Fields Virology. Vol. 2, 4th ed.; Lippincott–Williams & Wilkins; 2001. p.2579.
International Agency for Research on Cancer, World Health Organization. Epstein-Barr virus and Kaposi sarcoma herpes virus/human herpes virus 8. In: IARC monographs on the evaluation of carcinogenic risks to humans. Vol. 70. Lyon: IARC Press; 1997.
Burke AP, Yen TS, Shekitka KM, Sobin LH. Lymphoepithelial carcinoma of the stomach with Epstein-Barr virus demonstrated by polymerase chain reaction. Modern Pathol. 1990;3:377–80.
Shibata D, Weiss LM. Epstein Barr-virus-associated gastric adenocarcinoma. Am J Pathol. 1992;140:769–74.
Camargo MC, Koriyama C, Matsuo K, Kim WH, Herrera-Goepfert R, Liao LM, et al. Case–case comparison of smoking and alcohol risk associations with Epstein–Barr virus-positive gastric cancer. Int J Cancer. 2014;134:948–53.
Shinozaki-Ushiku A, Kunita A, Fukayama M. Update on Epstein-Barr virus and gastric cancer (review). Int J Oncol. 2015;46:1421–34.
Liu Y, Yang W, Pan Y, Ji J, Lu Z, Ke Y. Genome-wide analysis of Epstein-Barr virus (EBV) isolated from EBV-associated gastric carcinoma (EBVaGC). Oncotarget. 2016;7:4903–14.
Blaser MJ. Hypothesis: the changing relationships of Helicobacter pylori and humans: implications for health and disease. J Infect Dis. 1999;79:1523–30.
Palli D, Masala G, Del Giudice G, Plebani M, Basso D, Berti D, et al. CagA+ Helicobacter pylori infection and gastric cancer risk in the EPIC-EURGAST study. Int J Cancer. 2007;120:859–67.
Abadi ATB, Kusters JG. Management of Helicobacter pylori infections. BMC Gastroenterol. 2016;16:94.
Blaser MJ, Perez-Perez GI, Kleanthous H, Cover TL, Peek RM, Chyou PH, et al. Infection with Helicobacter pylori strains possessing cagA is associated with an increased risk of developing adenocarcinoma of the stomach. Cancer Res. 1995;55:2111–5.
Lauren P. The two histological main types of gastric carcinoma: diffuse and so-called intestinal-type carcinoma. An attempt at a histo-clinical classification. Acta Pathol Microbiol Scand. 1965;64:31–49.
AJCC Cancer Staging Manual. In: American Joint Committee on Cancer. Stomach. 6th ed. New York: NY: Springer; 2002. p. 99–106.
Drouet E, Brousset P, Fares F, Icart J, Verniol C, Meggetto F, et al. High Epstein-Barr virus serum load and elevated titers of anti-ZEBRA antibodies in patients with EBV-harboring tumor cells of Hodgkin's disease. J Med Virol. 1999;57:383–9.
Podzorski RP, Podzorski DS, Wuerth A, Tolia V. Analysis of the vacA, cagA, cagE, iceA, and babA2 genes in Helicobacter pylori from sixty-one pediatric patients from the Midwestern United States. Diagn Micr Infec Dis. 2003;46:83–8.
Saxena A, Nath Prasad K, Chand Ghoshal U, Krishnani N, Roshan Bhagat M, Husain N. Association of Helicobacter pylori and Epstein-Barr virus with gastric cancer and peptic ulcer disease. Scand J Gastroentero. 2008;43:669–74.
Shukla SK, Prasad KN, Tripathi A, Singh A, Saxena A, Ghoshal UC, et al. Epstein-Barr virus DNA load and its association with Helicobacter pylori infection in gastroduodenal diseases. Braz J Infect Dis. 2011;15:583–90.
Shukla SK, Prasad KN, Tripathi A, Ghoshal UC, Krishnani N, Husain N. Expression profile of latent and lytic transcripts of epstein–barr virus in patients with gastroduodenal diseases: a study from northern India. J Med Virol. 2012;84:1289–97.
Lee JH, Kim SH, Han SH, An JS, Lee ES, Kim YS. Clinicopathological and molecular characteristics of Epstein-Barr virus-associated gastric carcinoma: a meta-analysis. J Gastroen Hepatol. 2009;24:354–65.
zur Hausen A, Brink AA, Craanen ME, Middeldorp JM, Meijer CJ, van den Brule AJ. Unique transcription pattern of Epstein-Barr virus (EBV) in EBV-carrying gastric adenocarcinomas: expression of the transforming BARF1 gene. Cancer Res. 2000;60:2745–8.
Herrera-Goepfert R, Akiba S, Koriyama C, Ding S, Reyes E, Itoh T, et al. Epstein-Barr virus-associated gastric carcinoma: evidence of age-dependence among a Mexican population. World J Gastroentero. 2005;11:6096–103.
Murphy G, Pfeiffer R, Camargo MC, Rabkin CS. Meta-analysis shows that prevalence of Epstein-Barr virus-positive gastric cancer differs based on sex and anatomic location. Gastroenterology. 2009;137:824–33.
Corvalan A, Koriyama C, Akiba S, Eizuru Y, Backhouse C, Palma M, et al. Epstein-Barr virus in gastric carcinoma is associated with location in the cardia and with a diffuse histology: a study in one area of Chile. Int J Cancer. 2001;94:527–30.
Chen XZ, Chen H, Castro FA, Hu JK, Brenner H. Epstein–Barr virus infection and gastric cancer: a systematic review. Medicine. 2015;94:e792.
Zhao J, Jin H, Cheung KF, Tong JH, Zhang S, Go MY, et al. Zinc finger E-box binding factor 1 plays a central role in regulating Epstein-Barr virus (EBV) latent-lytic switch and acts as a therapeutic target in EBV-associated gastric cancer. Cancer. 2012;118:924–36.
van Beek J, zur Hausen A, Klein Kranenbarg E, van de Velde CJ, Middeldorp JM, van den Brule AJ, et al. EBV-positive gastric adenocarcinomas: a distinct clinico-pathologic entity with a low frequency of lymph node involvement. J Clin Oncol. 2004;22:664–70.
Genitsch V, Novotny A, Seiler CA, Kröll D, Walch A, Langer R. Epstein–Barr virus in gastro-esophageal adenocarcinomas–single center experiences in the context of current literature. Front Oncol. 2015;5:73.
Koriyama C, Akiba S, Minakami Y, Eizuru Y. Environmental fators related to Epstein-Barr virus-associated gastric cancer in Japan. J Exp Clin Canc Res. 2005;24:547–53.
Lima VP, de Lima MA, André AR, Ferreira MV, Barros MA, Rabenhorst SH. H pylori (CagA) and Epstein-Barr virus infection in gastric carcinomas: correlation with p53 mutation and c-Myc, Bcl-2 and Bax expression. World J Gastroentero. 2008;14:884–91.
Liu X, Liu J, Qiu H, Kong P, Chen S, Li W, et al. Prognostic significance of Epstein-Barr virus infection in gastric cancer: a meta-analysis. BMC Cancer. 2015;15:782.
Atherton JC, Blaser MJ. Coadaptation of Helicobacter pylori and humans: ancient history, modern implications. J Clin Invest. 2009;119:2475–87.
Backert S, Blaser MJ. The role of CagA in the gastric biology of Helicobacter pylori. Cancer Res. 2016;76:4028–31.
Bornschein J, Selgrad M, Warnecke M, Kuester D, Wex T, Malfertheiner P. H. Pylori infection is a key risk factor for proximal gastric cancer. Digest Dis Sci. 2010;55:3124–31.
Leja M, Axon A, Brenner H. (2016). Epidemiology of Helicobacter pylori infection. Helicobacter. 2016;21:3–7.
Peleteiro B, Lopes C, Figueiredo C, Lunet N. Salt intake and gastric cancer risk according to Helicobacter pylori infection, smoking, tumour site and histological type. Br J Cancer. 2011;104:198–207.
Kokkola A, Kosunen TU, Puolakkainen P, Sipponen P, Harkonen M, Laxen F, et al. Spontaneous disappearance of Helicobacter pylori antibodies in patients with advanced atrophic corpus gastritis. APMIS. 2003;111:619–24.
Nomura A, Stemmermann GN, Chyou PH, Kato I, Perez-Perez GI, Blaser MJ. Helicobacter pylori infection and gastric carcinoma among Japanese Americans in Hawaii. New Engl J Med. 1991;325:1132–6.
Crew KD, Neugut AI. Epidemiology of gastric cancer. World J Gastroentero. 2006;12:354–62.
Kang SY, Han JH, Ahn MS, Lee HW, Jeong SH, Park JS, et al. Helicobacter pylori infection as an independent prognostic factor for locally advanced gastric cancer patients treated with adjuvant chemotherapy after curative resection. Int J Cancer. 2012;130:948–58.
Marrelli D, Pedrazzani C, Berardi A, Corso G, Neri A, Garosi L, et al. Negative Helicobacter pylori status is associated with poor prognosis in patients with gastric cancer. Cancer. 2009;115:2071–80.
Wang F, Sun G, Zou Y, Zhong F, Ma T, Li X. Protective role of Helicobacter pylori infection in prognosis of gastric cancer: evidence from 2454 patients with gastric cancer. PLoS One. 2013;8:e62440.
Bamford KB, Fan X, Crowe SE, Leary JF, Gourley WK, Luthra GK, et al. Lymphocytes in the human gastric mucosa during Helicobacter pylori have a T helper cell 1 phenotype. Gastroenterology. 1998;114:482–92.
Xue LJ, Su QS, Yang JH, Lin Y. Autoimmune responses induced by Helicobacter pylori improve the prognosis of gastric carcinoma. Med Hypotheses. 2008;70:273–6.
Wu MS, Lee CW, Sheu JC, Shun CT, Wang HP, Hong RL, et al. Alterations of BAT-26 identify a subset of gastric cancer with distinct clinicopathologic features and better postoperative prognosis. Hepato-gastroenterol. 2002;49:285–9.
Kim Y, Shin A, Gwack J, Ko KP, Kim CS, Park SK, et al. Epstein-Barr virus antibody level and gastric cancer risk in Korea: a nested case-control study. Br J Cancer. 2009;101:526–9.
Luo B, Wang Y, Wang XF, Gao Y, Huang BH, Zhao P. Correlation of Epstein-Barr virus and its encoded proteins with Helicobacter pylori and expression of c-met and c-myc in gastric carcinoma. World J Gastroenterol. 2006;12:1842–8.
de Souza CR, de Oliveira KS, Ferraz JJ, Leal MF, Calcagno DQ, Seabra AD, et al. Occurrence of Helicobacter pylori and Epstein-Barr virus infection in endoscopic and gastric cancer patients from northern Brazil. BMC Gastroenterol. 2014;14:179.
Camargo MC, Kim KM, Matsuo K, Torres J, Liao LM, Morgan DR, et al. Anti-Helicobacter pylori antibody profiles in Epstein-Barr virus (EBV)-positive and EBV-negative gastric cancer. Helicobacter. 2016;21:153–7.
Minoura-Etoh J, Gotoh K, Sato R, Ogata M, Kaku N, Fujioka T, et al. Helicobacter pylori associated oxidant monochloramine induces reactivation of Epstein-Barr virus (EBV) in gastric epithelial cells latently infected with EBV. J Med Microbiol. 2006;55:905–11.
Ferrasi AC, Pinheiro NA, Rabenhorst SH, Caballero OL, Rodrigues MA, de Carvalho F, et al. Helicobacter pylori and EBV in gastric carcinomas: methylation status and microsatellite instability. World J Gastroentero. 2010;16:312–9.
Cárdenas-Mondragón MG, Carreon-Talavera R, Camorlinga-Ponce M, Gomez-Delgado A, Torres J, Fuentes-Panana EM. Epstein Barr virus and Helicobacter pylori co-infection are positively associated with severe gastritis in pediatric patients. PLoS One. 2013;8:e62850.
Cárdenas-Mondragón MG, Torres J, Flores-Luna L, Camorlinga-Ponce M, Carreón-Talavera R, Gomez-Delgado A, et al. Case–control study of Epstein–Barr virus and Helicobacter pylori serology in Latin American patients with gastric disease. Br J Cancer. 2015;112:1866–73.
Churin Y, Al-Ghoul L, Kepp O, Meyer TF, Birchmeier W, Naumann M. Helicobacter pylori CagA protein targets the c-met receptor and enhances the motogenic response. J Cell Biol. 2003;161:249–55.
Saju P, Murata-Kamiya N, Hayashi T, Senda Y, Nagase L, Noda S. Host SHP1 phosphatase antagonizes Helicobacter pylori CagA and can be downregulated by Epstein-Barr virus. Nat Microbiol. 2016;1:16026.
The authors would like to thank the patients and the supporting staff in this study. We are indebted to Professor Lina Carvalho from Faculty of Medicine of the University of Coimbra for kindly allow us to use the Bond Max equipment.
This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
Written informed consent was obtained from each patient; ethics approval was obtained from the Ethics Committees ofCoimbra University Hospital and Regional Oncology Center of Coimbra, Portugal.
Consent for publication
The authors declare that they have no competing interests.
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Nogueira, C., Mota, M., Gradiz, R. et al. Prevalence and characteristics of Epstein–Barr virus-associated gastric carcinomas in Portugal. Infect Agents Cancer 12, 41 (2017). https://doi.org/10.1186/s13027-017-0151-8
- Gastric cancer
- Epstein-Barr virus
- Helicobacter pylori
- Clinicopathologic feature