4.7 Article

Activation of human telomerase reverse transcriptase through gene fusion in clear cell sarcoma of the kidney

期刊

CANCER LETTERS
卷 357, 期 2, 页码 498-501

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.canlet.2014.11.057

关键词

TERT; IRX2; RNA sequencing; Pediatric kidney tumors; Fusion transcript

类别

资金

  1. Swedish Childhood Cancer Foundation [PROJ 2013-0011]
  2. Swedish Cancer Society [CAN 2012/318]
  3. Swedish Research Council [2013-2543]
  4. Crafoord Foundation
  5. Gunnar Nilsson Cancer Foundation
  6. Royal Physiographic Society
  7. BioCare Sweden

向作者/读者索取更多资源

Clear cell sarcoma of the kidney (CCSK) is a rare tumor type affecting infants and young children. Most CCSKs display few genomic aberrations, and no general underlying mechanism for tumor initiation has yet been identified, although a YWHAE-NUTM2B/NUTM2E fusion gene has been observed in a minority of cases. We performed RNA-sequencing of 22 CCSKs to investigate the presence of additional fusion transcripts. The presence of the YWHAE-NUTM2B/NUTM2E fusion was confirmed in two cases. In addition, a novel IRX2-TERT fusion transcript was identified in one case. SNP-array analyses revealed the underlying event to be an interstitial deletion in the short arm of chromosome 5 (5p15.33). TERT was dramatically upregulated under the influence of the IRX2 promoter. In line with TERT expression being driven by active IRX2 regulatory elements, we found a high expression of IRX2 in CCSKs irrespective of fusion gene status. IRX2 was also expressed in human fetal kidney - the presumed tissue of origin for CCSK. We conclude that in addition to promoter mutations and epigenetic events, TERT can also be activated in tumors via formation of fusion transcripts. (C) 2014 Elsevier Ireland Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据