Amplification and Overexpression of c-met Gene in Epstein-Barr Virus-Associated Gastric Carcinomas (original) (raw)

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Research Articles| January 24 2002

Yuko Kijima;

aFirst Department of Surgery,

bDivision of Persistent and Oncogenic viruses, Center for Chronic Viral Diseases, and

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Shuichi Hokita;

aFirst Department of Surgery,

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Heiji Yoshinaka;

aFirst Department of Surgery,

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Tetsuhiko Itoh;

dDepartment of Pathology, Kagoshima Medical Laboratory Center, Kagoshima, Japan

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Chihaya Koriyama;

cDepartment of Public Health, Faculty of Medicine, Kagoshima University, Kagoshima,

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Yoshito Eizuru;

bDivision of Persistent and Oncogenic viruses, Center for Chronic Viral Diseases, and

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Suminori Akiba;

cDepartment of Public Health, Faculty of Medicine, Kagoshima University, Kagoshima,

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Takashi Aikou

aFirst Department of Surgery,

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Oncology (2002) 62 (1): 60–65.

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Abstract

To reveal the role of oncogenes in Epstein-Barr virus (EBV)-positive gastric carcinomas, the amplification and overexpression of the c-met gene were examined by a competitive polymerase chain reaction and immunohistochemistry, respectively. The proportion of c-met amplification and overexpression in EBV-positive and -negative carcinomas did not differ significantly. The amplification and overexpression of the c-met gene in EBV-negative gastric carcinomas were significantly associated with upper location, deeper invasion and lymphatic invasion, while in EBV-positive gastric carcinomas a significant correlation with c-met activation was observed only in deeper invasion. However, none of the observed associations of c-met amplification or overexpression with clinicopathological features in the EBV-positive and -negative carcinomas differed significantly in their strength or direction. These results suggest that the amplification and overexpression of c-met gene do not play a different role in the progression and metastasis of EBV-positive and EBV-negative gastric carcinomas.

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© 2002 S. Karger AG, Basel

2002

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