Volume 105, Issue 3 pp. 764-767

Establishment of a near-triploid human B-cell lymphoma cell line with t(14;18) and a p53 gene point mutation

Hiroki Yamaguchi

Hiroki Yamaguchi

Division of Haematology, Department of Internal Medicine, Nippon Medical School, Tokyo, Japan

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Koiti Inokuchi

Koiti Inokuchi

Division of Haematology, Department of Internal Medicine, Nippon Medical School, Tokyo, Japan

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Hideki Hanawa

Hideki Hanawa

Division of Haematology, Department of Internal Medicine, Nippon Medical School, Tokyo, Japan

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Sakae Tanosaki

Sakae Tanosaki

Division of Haematology, Department of Internal Medicine, Nippon Medical School, Tokyo, Japan

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Isao Shinozawa

Isao Shinozawa

Division of Haematology, Department of Internal Medicine, Nippon Medical School, Tokyo, Japan

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Hiroki Matuoka

Hiroki Matuoka

Division of Haematology, Department of Internal Medicine, Nippon Medical School, Tokyo, Japan

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Kazuo Dan

Kazuo Dan

Division of Haematology, Department of Internal Medicine, Nippon Medical School, Tokyo, Japan

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First published: 25 December 2001
Citations: 5
Dr Koiti Inokuchi, Division of Haematology, Department of Internal Medicine, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, Tokyo 113-8603, Japan.

Abstract

We report a rare large B-cell non-Hodgkin's lymphoma having a characteristic near-triploid cell population with add(17)(p22) and t(14;18)(q32;q21) translocation. We also established and characterized a new cell line (TK cell) derived from the present lymphoma. A codon 180 mutation (GAG → GAT) in the p53 gene was detected. t(14;18)(q32;q21) was revealed juxtaposition of the bcl-2 and JH genes. Immunoprecipitation analyses of p53 and bcl-2 revealed that abnormality of the p53 protein and aberrant bcl-2 expression, which may protect cells from apoptosis, may be critical to the development of leukaemogenesis exhibiting near-triploid chromosomes.

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