Abstract

Background : Epstein–Barr virus (EBV)-associated gastric carcinomas (GC) constitute a distinct clinicopathological entity of gastric cancer. In order to determine underlying distinct aberrant promoter methylation we tested cardiac and non-cardiac GC with regard to the presence of EBV. Methods : One hundred GC were tested by RNA-in situ hybridization for the presence of EBV by EBV-encoded small RNA (EBER). Aberrant promoter methylation was investigated by methylation-specific real-time PCR for p16, p14, APC and hMLH1. P16 protein expression was assessed by immunohistochemistry. Results : In our selected study cohort, EBER-transcripts were detected in 19.6% (18/92) of GC. EBV-positive GC revealed significantly more often gene hypermethylation of p16, p14 and APC (p < 0.0001, p < 0.0001 and p = 0.02, respectively) than EBV-negative GC. The majority of GC with p16 hypermethylation showed a p16 protein loss (22/28). In contrast, no correlation between the presence of EBV and hMLH1 hypermethylation was found (p = 0.7). EBV-positive GC showed a trend towards non-cardiac location (p = 0.06) and lower stages (I/II) according to the WHO (p = 0.05). Conclusion : Hypermethylation of tumor suppressor genes is significantly more frequent in EBV-associated GC compared to EBV-negative GC. Our data add new insights to the role of EBV in gastric carcinogenesis and underline that EBV-associated GC comprise a distinct molecular-pathologic as well as a distinct clinicopathological entity of GC.

Keywords

MethylationDNA methylationCarcinogenesisBiologyImmunohistochemistryCancerPromoterCancer researchEpstein–Barr virusMolecular biologyGeneVirusGene expressionVirologyImmunologyGenetics

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Year
2010
Type
article
Volume
33
Issue
3-4
Pages
143-149
Citations
24
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Helene Geddert, Axel zur Hausen, Helmut E. Gabbert et al. (2010). EBV-Infection in Cardiac and Non-Cardiac Gastric Adenocarcinomas is Associated with Promoter Methylation of<i>p16</i>,<i>p14</i>and<i>APC</i>, but not<i>hMLH1</i>. Analytical Cellular Pathology , 33 (3-4) , 143-149. https://doi.org/10.1155/2010/453764

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DOI
10.1155/2010/453764