Establishment of CD5 and CD10 double-positive mature B-cell line, WILL1, showing complex 8q24 translocation involving 14q32 and 6q27

被引:1
|
作者
Uneda, Shima [1 ]
Gotoh, Minako [2 ]
Sonoki, Takashi [1 ]
Nishida, Kazuhiro [2 ]
Nakamura, Yasushi [3 ]
Kurimoto, Miwa [1 ]
Hanaoka, Nobuyoshi [1 ]
Matsuoka, Hiroshi [1 ]
Taniwaki, Masafumi [2 ]
Nakakuma, Hideki [1 ]
机构
[1] Wakayama Med Univ, Dept Hematol Oncol, Wakayama 6418510, Japan
[2] Kyoto Prefectural Univ Med, Dept Hematol & Oncol, Kyoto, Japan
[3] Wakayama Med Univ, Dept Clin Lab Med, Wakayama, Japan
关键词
Lymphoma; CD5; CD10; Translocation; 8q24; 6q27;
D O I
10.1007/s12185-008-0189-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We established a novel mature B-cell line from a CD5 and CD10 double-positive diffuse large B-cell lymphoma patient, designated as WILL1. WILL1 cells were positive for CD5, CD10, CD19, and CD20. Spectral karyotype (SKY) analysis revealed chromosome 8 signals on 6q27 as well as 14q32. Fluorescence in situ hybridization (FISH) analysis suggested that a translocation break occurred outside the immunoglobulin heavy chain (IGH) gene on 14q32. Moreover, fusion signals of IGH and C-MYC probes were detected on the derivative 6 and derivative 14 chromosomes. Southern blot analysis using a C-MYC exon II fragment failed to detect rearrangement, suggesting that the 8q24 breakpoints lay far up- or downstream of the C-MYC gene. WILL1 is a useful tool to analyze the pathogenesis of CD5 and CD10 double-positive diffuse large B-cell lymphoma, and for molecular cloning of the unique translocation breakpoints of 14q32 and 8q24 and a novel gene on 6q27.
引用
收藏
页码:536 / 542
页数:7
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