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Genetic alterations of JAK/STAT cascade and histone modification in extranodal NK/T-cell lymphoma nasal type

Authors
Lee S.[Lee S.]Park H.Y.[Park H.Y.]Kang S.Y.[Kang S.Y.]Kim S.J.[Kim S.J.]Hwang J.[Hwang J.]Lee S.[Lee S.]Kwak S.H.[Kwak S.H.]Park K.S.[Park K.S.]Yoo H.Y.[Yoo H.Y.]Kim W.S.[Kim W.S.]Kim J.-I.[Kim J.-I.]Ko Y.H.[Ko Y.H.]
Issue Date
2015
Keywords
Chromatin modification; Extranodal NK/T-cell lymphoma nasal type; JAK-STAT pathway; Next-generation sequencing; Somatic mutation
Citation
Oncotarget, v.6, no.19, pp.17764 - 17776
Journal Title
Oncotarget
Volume
6
Number
19
Start Page
17764
End Page
17776
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/50240
Abstract
Extranodal NK/T-cell lymphoma nasal type (ENKL) is a rare type of non-Hodgkin lymphoma that more frequently occurs in East Asia and Latin America. Even though its molecular background has been discussed in the last few years, the current knowledge does not explain the disease pathogenesis in most cases of ENKL. Here, we performed multiple types of next-generation sequencing on 34 ENKL samples, including whole-exome sequencing (9 cancer tissues and 4 cancer cell lines), targeted sequencing (21 cancer tissues), and RNA sequencing (3 cancer tissues and 4 cancer cell lines). Mutations were found most frequently in 3 genes, STAT3, BCOR, and MLL2 (which were present in 9, 7, and 6 cancer samples, respectively), whereas there were only 2 cases of JAK3 mutation. In total, JAK/STAT pathway- and histone modification-related genes accounted for 55.9% and 38.2% of cancer samples, respectively, and their involvement in ENKL pathogenesis was also supported by gene expression analysis. In addition, we provided 177 genes upregulated only in cancer tissues, which appear to be linked with angiocentric and angiodestructive growth of ENKL. In this study, we propose several novel driver genes of ENKL, and show that these genes and their functional groups may be future therapeutic targets of this disease.
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