Identification by FFPE RNA‐Seq of a new recurrent inversion leading to RBM10‐TFE3 fusion in renal cell carcinoma with subtle TFE3 break‐apart FISH pattern. Issue 6 (7th April 2016)
- Record Type:
- Journal Article
- Title:
- Identification by FFPE RNA‐Seq of a new recurrent inversion leading to RBM10‐TFE3 fusion in renal cell carcinoma with subtle TFE3 break‐apart FISH pattern. Issue 6 (7th April 2016)
- Main Title:
- Identification by FFPE RNA‐Seq of a new recurrent inversion leading to RBM10‐TFE3 fusion in renal cell carcinoma with subtle TFE3 break‐apart FISH pattern
- Authors:
- Just, Pierre‐Alexandre
Letourneur, Franck
Pouliquen, Christelle
Dome, Florence
Audebourg, Anne
Biquet, Philippe
Vidaud, Michel
Terris, Benoit
Sibony, Mathilde
Pasmant, Eric - Abstract:
- Abstract : Gene fusions involving TFE3 defines the "Xp11.2 translocations" subclass of renal cell carcinomas (RCCs) belonging to the MiT family translocation RCC. Four recurrent TFE3 fusion partners were identified to date: PRCC, ASPSCR1, SFPQ, and NONO . Break‐apart TFE3 fluorescence in situ hybridization (FISH) on formalin‐fixed and paraffin‐embedded (FFPE) tissue sections is currently the gold standard for identification of TFE3 rearrangements. Herein, we report a case of RCC with a morphological appearance of Xp11.2 translocation, and positive TFE3 immunostaining. By FISH, the spots constituting the split signal were barely spaced, suggestive of a chromosome X inversion rather than a translocation. We performed RNA‐seq from FFPE material to test this hypothesis. RNA‐seq suggested a fusion of RBM10 gene exon 17 (Xp11.23) with TFE3 gene exon 5 (Xp11.2). RBM10‐TFE3 fusion transcript was confirmed using specific RT‐PCR. Our work showed that RNA‐Seq is a robust technique to detect fusion transcripts from FFPE material. A RBM10‐TFE3 fusion was previously described in single case of Xp11.2 RCC. Although rare, RBM10‐TFE3 fusion variant (from chromosome X paracentric inversion), therefore, appears to be a recurrent molecular event in Xp11.2 RCCs. RBM10‐TFE3 fusion should be added in the list of screened fusion transcripts in targeted molecular diagnostic multiplex RT‐PCR. © 2016 Wiley Periodicals, Inc.
- Is Part Of:
- Genes, chromosomes & cancer. Volume 55:Issue 6(2016:Jun.)
- Journal:
- Genes, chromosomes & cancer
- Issue:
- Volume 55:Issue 6(2016:Jun.)
- Issue Display:
- Volume 55, Issue 6 (2016)
- Year:
- 2016
- Volume:
- 55
- Issue:
- 6
- Issue Sort Value:
- 2016-0055-0006-0000
- Page Start:
- 541
- Page End:
- 548
- Publication Date:
- 2016-04-07
- Subjects:
- Cancer -- Genetic aspects -- Periodicals
616.994042 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1098-2264 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/gcc.22356 ↗
- Languages:
- English
- ISSNs:
- 1045-2257
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4111.763000
British Library DSC - BLDSS-3PM
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- 1307.xml