MUTATIONAL ANALYSIS OF THE CDKN2 (MTS1/P16(INK4A)) GENE IN PRIMARY B-CELL LYMPHOMAS

被引:60
|
作者
UCHIDA, T [1 ]
WATANABE, T [1 ]
KINOSHITA, T [1 ]
MURATE, T [1 ]
SAITO, H [1 ]
HOTTA, T [1 ]
机构
[1] NAGOYA UNIV,SCH MED,DEPT INTERNAL MED 1,SHOWA KU,NAGOYA,AICHI 466,JAPAN
关键词
D O I
10.1182/blood.V86.7.2724.bloodjournal8672724
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The CDKN2 gene located on chromosome 9p21 encodes the cyclin-dependent kinase-4 inhibitor pig. This gene is a putative tumor-suppressor gene because of its frequent alterations in many kinds of tumor cell lines. We analyzed the CDKN2 gene to evaluate its alterations in 52 primary specimens of non-Hodgkin's lymphoma (NHL) or chronic lymphocytic leukemia (CLL) of B-cell origin by Southern blot analysis, polymerase chain reaction-mediated single-strand conformation polymorphism (PCR-SSCP) analysis, and direct sequencing. By Southern blot analysis, we showed homozygous deletion of the CDKN2 gene in 3 of 42 patients with B-NHL (7.1%). After screening by PCR-SSCP analysis, direct sequencing identified one missense mutation at codon 72 (nucleotide 233) and two frameshifts due to a 35-bp deletion arising at codon 3 (nucleotides 27 to 61) and a 13-bp deletion arising at codon 49 (nucleotides 163 to 175) in patients with B-NHL (3 of 42, 7.1%). In the patient carrying the missense mutation, hemizygous deletion of the CDKN2 gene was also suspected. In this study, we detected alterations in CDKN2 in 6 of 42 patients (14.3%) with B-NHL and in none of 10 patients with B-CLL. Our results suggest that the CDKN2 alterations contribute in tumorigenesis in some patients with B-NHL. (C) 1995 by The American Society of Hematology.
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页码:2724 / 2731
页数:8
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