Allelotype Analysis of Adult T-Cell Leukemia

Author:

Hatta Yoshihiro1,Yamada Yasuaki1,Tomonaga Masao1,Said Jonathan W.1,Miyosi Isao1,Koeffler H. Phillip1

Affiliation:

1. From the Division of Hematology/Oncology, Cedars-Sinai Research Institute, UCLA School of Medicine, Los Angeles, CA; the Deparment of Laboratoy Medicine and the Department of Hematology, Nagasaki University School of Medicine, Nagasaki, Japan; the Department of Pathology, Center for the Health Science, UCLA School of Medicine, Los Angeles, CA; and the Department of Medicine, Kochi Medical School, Kochi, Japan.

Abstract

Abstract Allelotype analysis of adult T-cell leukemia (ATL) was undertaken for the first time to identify chromosomal loci relevant to the development of acute/lymphomatous ATL. Loss of heterozygosity (LOH) was screened using 94 highly polymorphic microsatellite markers, distributed among all nonacrocentric, autosomal chromosomes. In each of the 22 cases, DNA obtained from their leukemic cells in acute/lymphomatous phase was compared with their constitutional DNA from mononuclear cells in chronic or remission phase. Allelic losses of at least on one chromosome arm occurred in 91% of the cases (20 individuals). Among 39 chromosome arms, allelic losses were observed on 31 arms at least for one sample. A high frequency of allelic loss (>30%) was seen on chromosome arms 6q (41%) and 17p (48%). The mean fractional allelic loss (FAL) was 0.109. These findings suggest that a novel tumor suppressor gene on chromosome arm 6q, as well as the p53 gene on chromosome arm 17p, probably have an important role in the development of acute/lymphomatous ATL. © 1998 by The American Society of Hematology.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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