Identification of a novel fusion, SQSTM1-ALK, in ALK-positive large B-cell lymphoma

被引:75
|
作者
Takeuchi, Kengo [1 ]
Soda, Manabu [2 ]
Togashi, Yuki
Ota, Yasunori [3 ]
Sekiguchi, Yasunobu [4 ]
Hatano, Satoko
Asaka, Reimi
Noguchi, Masaaki [4 ]
Mano, Hiroyuki [2 ,5 ]
机构
[1] Japanese Fdn Canc Res, Inst Canc, Pathol Project Mol Targets, Koto Ku, Tokyo 1358550, Japan
[2] Jichi Med Univ, Div Funct Genom, Utsunomiya, Tochigi, Japan
[3] Toranomon Gen Hosp, Dept Pathol, Tokyo, Japan
[4] Juntendo Univ, Urayasu Hosp, Dept Hematol, Chiba, Japan
[5] Japan Sci & Technol Agcy, CREST, Saitama, Japan
来源
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL | 2011年 / 96卷 / 03期
关键词
ALK-positive; large B-cell lymphoma; fusion; LUNG-CANCER; SELECTIVE AUTOPHAGY; GENE; TRANSLOCATION; KINASE; P62/SQSTM1; EXPRESSION; RARE; CLTC;
D O I
10.3324/haematol.2010.033514
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
ALK-positive large B-cell lymphoma is a rare subtype of lymphoma, and most cases follow an aggressive clinical course with a poor prognosis. We examined an ALK-positive large B-cell lymphoma case showing an anti-ALK immunohistochemistry pattern distinct from those of 2 known ALK fusions, CLTC-ALK and NPM-ALK, for the presence of a novel ALK fusion; this led to the identification of SQSTM1-ALK. SQSTM1 is an ubiquitin binding protein that is associated with oxidative stress, cell signaling, and autophagy. We showed transforming activities of SQSTM1-ALK with a focus formation assay and an in vivo tumorigenicity assay using 3T3 fibroblasts infected with a recombinant retrovirus encoding SQSTM1-ALK. ALK-inhibitor therapies are promising for treating ALK-positive large B-cell lymphoma, especially for refractory cases. SQSTM1-ALK may be a rare fusion, but our data provide novel biological insights and serve as a key for the accurate diagnosis of this rare lymphoma.
引用
收藏
页码:464 / 467
页数:4
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