4.7 Article

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

Journal

CANCER LETTERS
Volume 357, Issue 2, Pages 498-501

Publisher

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

Keywords

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

Categories

Funding

  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

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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.

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