Fusion of the genes ataxin 2 like, ATXN2L, and Janus kinase 2, JAK2, in cutaneous CD4 positive T-cell lymphoma

被引:16
作者
Panagopoulos, Ioannis [1 ]
Gorunova, Ludmila [1 ]
Spetalen, Signe [2 ]
Bassarova, Assia [2 ]
Beiske, Klaus [2 ]
Micci, Francesca [1 ]
Heim, Sverre [1 ,3 ]
机构
[1] Oslo Univ Hosp, Inst Canc Genet & Informat, Norwegian Radium Hosp, Sect Canc Cytogenet, Oslo, Norway
[2] Oslo Univ Hosp, Norwegian Radium Hosp, Dept Pathol, Oslo, Norway
[3] Univ Oslo, Fac Med, Oslo, Norway
关键词
primary cutaneous CD4 positive T-cell lymphoma; cytogenetics; RNA-sequencing; ATXN2L-JAK2 fusion gene; PCM1-JAK2; FUSION; IN-VITRO; RUXOLITINIB; MUTATIONS; PROTEIN; CLASSIFICATION; EFFICACY; DOMAIN;
D O I
10.18632/oncotarget.21790
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Acquired mutations were recently described in cutaneous T-cell lymphomas for the JAK1, JAK3, STAT3, and STAT5B genes of the JAK-STAT pathway. In the present study, RNA-sequencing of a primary cutaneous CD4 positive T-cell lymphoma carrying a three-way t(9; 13; 16)(p24; q34; p11) chromosome translocation showed that JAK2 from chromosome band 9p24 was rearranged and fused to a novel partner gene, ATXN2L, from 16p11. RT-PCR together with Sanger sequencing verified the presence of the ATXN2L-JAK2 fusion transcript. The ATXN2L-JAK2 fusion gene would code for a chimeric protein containing all domains of ATXN2L and the catalytic domain of the JAK2 tyrosine kinase. The ATXN2L-JAK2 chimeric protein could lead to constitutive activation of the downstream JAK-STAT signaling pathway in a manner similar to that seen for other JAK2 fusion proteins.
引用
收藏
页码:103775 / 103784
页数:10
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