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Monoclonal Epstein‐Barr virus genomes but lack of EBV‐related protein expression in different types of gastric carcinoma
Author(s) -
OTT G.,
KIRCHNER TH.,
MÜLLERHERMELINK H.K.
Publication year - 1994
Publication title -
histopathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.626
H-Index - 124
eISSN - 1365-2559
pISSN - 0309-0167
DOI - 10.1111/j.1365-2559.1994.tb01350.x
Subject(s) - nasopharyngeal carcinoma , biology , in situ hybridization , epstein–barr virus , pathology , virus , carcinoma , immunohistochemistry , blot , infiltration (hvac) , monoclonal , monoclonal antibody , microbiology and biotechnology , gene , antibody , messenger rna , virology , immunology , medicine , biochemistry , physics , thermodynamics , radiation therapy
Thirty‐nine resection specimens of gastric carcinomas have been investigated for the presence of EBV RNA sequences using a highly sensitive non‐radioactive in situ hybridization technique. Transcribed EBER sequences were found in seven (18%), including four cases of undifferentiated carcinoma with prominent lymphoid infiltration and three gastric adenocarcinomas. In the positive tumours all, or nearly all, tumour nuclei were distinctly labelled. No positive signals could be detected in the non‐dysplastic epithelial cells or the reactive inflammatory infiltrate. Clonality analysis using specific probes to the variable tandem repeat region of the EBV yielded single episomal bands in all four cases tested, two of which were undifferentiated carcinomas and two adenocarcinomas. By means of immunohistology, no expression of the EBV‐related proteins LMP or EBNA‐2 was present in tumour cells of positive cases in in situ or blotting attempts. Our results suggest that infection of gastric carcinomas by the EB virus occurs early in tumourigenesis but, in contrast to nasopharyngeal carcinomas, does not result in the expression of EBV‐specific proteins.