生物
成人T细胞白血病/淋巴瘤
癌症研究
T细胞白血病
白血病
相互作用体
免疫监视
T细胞
转录组
Jurkat细胞
癌症
遗传学
基因
基因表达
免疫系统
作者
Keisuke Kataoka,Yasunobu Nagata,Akira Kitanaka,Yuichi Shiraishi,Teppei Shimamura,Jun‐ichirou Yasunaga,Yasushi Totoki,Kenichi Chiba,Aiko Sato‐Otsubo,Genta Nagae,Ryohei Ishii,Satsuki Muto,Shinichi Kotani,Yosaku Watatani,June Takeda,Masashi Sanada,Hiroko Tanaka,Hiromichi Suzuki,Yusuke Sato,Yusuke Shiozawa
出处
期刊:Nature Genetics
[Nature Portfolio]
日期:2015-10-05
卷期号:47 (11): 1304-1315
被引量:740
摘要
Adult T cell leukemia/lymphoma (ATL) is a peripheral T cell neoplasm of largely unknown genetic basis, associated with human T cell leukemia virus type-1 (HTLV-1) infection. Here we describe an integrated molecular study in which we performed whole-genome, exome, transcriptome and targeted resequencing, as well as array-based copy number and methylation analyses, in a total of 426 ATL cases. The identified alterations overlap significantly with the HTLV-1 Tax interactome and are highly enriched for T cell receptor-NF-κB signaling, T cell trafficking and other T cell-related pathways as well as immunosurveillance. Other notable features include a predominance of activating mutations (in PLCG1, PRKCB, CARD11, VAV1, IRF4, FYN, CCR4 and CCR7) and gene fusions (CTLA4-CD28 and ICOS-CD28). We also discovered frequent intragenic deletions involving IKZF2, CARD11 and TP73 and mutations in GATA3, HNRNPA2B1, GPR183, CSNK2A1, CSNK2B and CSNK1A1. Our findings not only provide unique insights into key molecules in T cell signaling but will also guide the development of new diagnostics and therapeutics in this intractable tumor.
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