Epstein-barr virus in gastric carcinoma

The Epstein-Barr virus (EBV) is detected in about 10% of gastric carcinoma cases throughout the world. In EBV-associated gastric carcinoma, all tumor cells harbor the clonal EBV genome. Gastric carcinoma associated with EBV has distinct clinicopathological features, occurs predominately in men and i...

Full description

Saved in:
Bibliographic Details
Published inCancers Vol. 6; no. 4; pp. 2259 - 2274
Main Authors Nishikawa, Jun, Yoshiyama, Hironori, Iizasa, Hisashi, Kanehiro, Yuichi, Nakamura, Munetaka, Nishimura, Junichi, Saito, Mari, Okamoto, Takeshi, Sakai, Kouhei, Suehiro, Yutaka, Yamasaki, Takahiro, Oga, Atsunori, Yanai, Hideo, Sakaida, Isao
Format Journal Article Book Review
LanguageEnglish
Published Switzerland MDPI AG 07.11.2014
MDPI
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The Epstein-Barr virus (EBV) is detected in about 10% of gastric carcinoma cases throughout the world. In EBV-associated gastric carcinoma, all tumor cells harbor the clonal EBV genome. Gastric carcinoma associated with EBV has distinct clinicopathological features, occurs predominately in men and in younger-aged individuals, and presents a generally diffuse histological type. Most cases of EBV-associated gastric carcinoma exhibit a histology rich in lymphocyte infiltration. The immunological reactiveness in the host may represent a relatively preferable prognosis in EBV-positive cases. This fact highlights the important role of EBV in the development of EBV-associated gastric carcinoma. We have clearly proved direct infection of human gastric epithelialcells by EBV. The infection was achieved by using a recombinant EBV. Promotion of growth by EBV infection was observed in the cells. Considerable data suggest that EBV may directly contribute to the development of EBV-associated GC. This tumor-promoting effect seems to involve multiple mechanisms, because EBV affects several host proteins and pathways that normally promote apoptosis and regulate cell proliferation.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-3
content type line 23
ObjectType-Review-1
ObjectType-Article-1
ObjectType-Feature-2
ISSN:2072-6694
2072-6694
DOI:10.3390/cancers6042259