Title | Identification of recurrent NAB2-STAT6 gene fusions in solitary fibrous tumor by integrative sequencing. |
Publication Type | Journal Article |
Year of Publication | 2013 |
Authors | Robinson DR, Wu Y-M, Kalyana-Sundaram S, Cao X, Lonigro RJ, Sung Y-S, Chen C-L, Zhang L, Wang R, Su F, Iyer MK, Roychowdhury S, Siddiqui J, Pienta KJ, Kunju LP, Talpaz M, Mosquera JMiguel, Singer S, Schuetze SM, Antonescu CR, Chinnaiyan AM |
Journal | Nat Genet |
Volume | 45 |
Issue | 2 |
Pagination | 180-5 |
Date Published | 2013 Feb |
ISSN | 1546-1718 |
Keywords | Adult, Base Sequence, Cell Proliferation, Cells, Cultured, Chromatin Immunoprecipitation, DNA Mutational Analysis, Exome, Female, Fluorescent Antibody Technique, Gene Expression Regulation, Neoplastic, Gene Fusion, High-Throughput Nucleotide Sequencing, Humans, Immunoblotting, Luciferases, Models, Genetic, Molecular Sequence Data, Real-Time Polymerase Chain Reaction, Regulatory Elements, Transcriptional, Repressor Proteins, Reverse Transcriptase Polymerase Chain Reaction, Solitary Fibrous Tumors, STAT6 Transcription Factor, Transcriptome |
Abstract | A 44-year old woman with recurrent solitary fibrous tumor (SFT)/hemangiopericytoma was enrolled in a clinical sequencing program including whole-exome and transcriptome sequencing. A gene fusion of the transcriptional repressor NAB2 with the transcriptional activator STAT6 was detected. Transcriptome sequencing of 27 additional SFTs identified the presence of a NAB2-STAT6 gene fusion in all tumors. Using RT-PCR and sequencing, we detected this fusion in all 51 SFTs, indicating high levels of recurrence. Expression of NAB2-STAT6 fusion proteins was confirmed in SFT, and the predicted fusion products harbor the early growth response (EGR)-binding domain of NAB2 fused to the activation domain of STAT6. Overexpression of the NAB2-STAT6 gene fusion induced proliferation in cultured cells and activated the expression of EGR-responsive genes. These studies establish NAB2-STAT6 as the defining driver mutation of SFT and provide an example of how neoplasia can be initiated by converting a transcriptional repressor of mitogenic pathways into a transcriptional activator. |
DOI | 10.1038/ng.2509 |
Alternate Journal | Nat Genet |
PubMed ID | 23313952 |
Grant List | 5 P30 CA46592 / CA / NCI NIH HHS / United States P01 CA047179-15A2 / CA / NCI NIH HHS / United States P50 CA 140146-01 / CA / NCI NIH HHS / United States |
Related Faculty:
Juan Miguel Mosquera, M.D.