Volume 48, Issue 2 pp. 134-137

Transforming growth factor J3 type II receptor (TGFpRII) mutation in gastric lymphoma without mutator phenotype

Kazuhiko Yasuml

Kazuhiko Yasuml

The First Department of Pathology, Hamamatsu University School of Medicine, Hamamatsu, Japan

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Rong-Jun Guo

Rong-Jun Guo

The First Department of Pathology, Hamamatsu University School of Medicine, Hamamatsu, Japan

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Hiroyuki Hanai

Hiroyuki Hanai

The First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan

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Hajime Arai

Hajime Arai

The First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan

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Eizo Kaneko

Eizo Kaneko

The First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan

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Hiroyuki Konno

Hiroyuki Konno

The Second Department of Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan

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Selichi Takenoshita

Selichi Takenoshita

Laboratory of Human Carcinogenesis, National Cancer Institute, Bethesda, Maryland, United States of America

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Koichi Hagiwara

Koichi Hagiwara

Laboratory of Human Carcinogenesis, National Cancer Institute, Bethesda, Maryland, United States of America

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Haruhiko Sugimura

Corresponding Author

Haruhiko Sugimura

The First Department of Pathology, Hamamatsu University School of Medicine, Hamamatsu, Japan

The First Department of Pathology, Hamamatsu University School of Medicine, 3600 Handa cho, Hamamatsu 431–31, Japan. Email: <[email protected]>Search for more papers by this author
First published: 12 December 2008
Citations: 9

Abstract

A new mutation in the serine-threonine klnase domain of the transforming growth factor β type II receptor (TGFpRII) was found in a case of diffuse, B cell non-Hodgkin's lymphoma of the stomach. A mfssense mutation (ACA to GCA, Thr to Ala) was detected In exon 5, and a wild type allele was also present. This Is the first naturally occurring mutation in the klnase domain of this gene identified in human primary lymphoma. The replication error at three loci was negative, and the poly A tract of exon 3, which is frequently a target of mismatch repair genes, was intact. Malignant lymphoma of B cell origin in the stomach Is an addition to an expanding catalogue of tumors with TGFβRII alterations, and the biological sequelae of the change in the functional domain and the clinical characteristics of the patient in this study are intriguing.

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