Journal article
Anchored multiplex PCR for targeted next-generation sequencing reveals recurrent and novel USP6 fusions and upregulation of USP6 expression in aneurysmal bone cyst
Genes chromosomes & cancer, Vol.56(4), pp.266-277
04/2017
DOI: 10.1002/gcc.22432
PMID: 27910166
Abstract
Primary aneurysmal bone cyst (ABC) is a neoplastic process due to recurrent translocations involving the USP6 gene. By fluorescence in situ hybridization, up to 69% of primary ABCs harbored USP6 translocations; no USP6 translocation was found in secondary ABC or giant cell tumor of bone (GCT). GCT can recur locally, metastasize to the lungs in some cases, and rarely undergo malignant transformation. Differentiating primary ABC from its mimics is important for treatment and prognosis. We evaluated USP6 fusion and expression in 13 cases of primary and 1 case of secondary ABC, and 9 cases of GCT using nucleic acid extracted from formalin-fixed, paraffin-embedded tissue and a next generation sequencing (NGS)-based assay. USP6 fusions including 7 novel fusions and USP6 transcripts were identified in all 13 primary ABCs. Nine cases with strong evidence of fusions showed high levels of USP6 transcripts by reverse transcription-PCR (RT-PCR). The remaining four had no detectable USP6 expression by a first-round of RT-PCR but the presence of USP6 transcripts was identified by a second-round, nested PCR. The major fusions were confirmed by RT-PCR followed by Sanger sequencing. No USP6 fusion or transcript was detected in any of the GCTs or the case of secondary ABC by NGS or by two rounds of PCR. All USP6 translocations resulted in fusion of the entire USP6 coding sequence with promoters of the fusion gene leading to upregulation of USP6 transcription, which is likely the underlying mechanism for ABC oncogenesis. © 2016 Wiley Periodicals, Inc.
Details
- Title: Subtitle
- Anchored multiplex PCR for targeted next-generation sequencing reveals recurrent and novel USP6 fusions and upregulation of USP6 expression in aneurysmal bone cyst
- Creators
- Natalya V Guseva - Department of Pathology, University of Iowa Hospitals and Clinics, Iowa City, IA, 52242Omar Jaber - Department of Pathology, University of Iowa Hospitals and Clinics, Iowa City, IA, 52242Munir R Tanas - Department of Pathology, University of Iowa Hospitals and Clinics, Iowa City, IA, 52242Aaron A Stence - Department of Pathology, University of Iowa Hospitals and Clinics, Iowa City, IA, 52242Ramakrishna Sompallae - Iowa Institute of Human Genetics, University of Iowa, Iowa City, IA, 52242Jenna Schade - Department of Pathology, University of Iowa Hospitals and Clinics, Iowa City, IA, 52242Allison N Fillman - Department of Pathology, University of Iowa Hospitals and Clinics, Iowa City, IA, 52242Benjamin J Miller - Department of Orthopaedics and Rehabilitation, University of Iowa Hospitals and Clinics, Iowa City, IA, 52242Aaron D Bossler - Department of Pathology, University of Iowa Hospitals and Clinics, Iowa City, IA, 52242Deqin Ma - Department of Pathology, University of Iowa Hospitals and Clinics, Iowa City, IA, 52242
- Resource Type
- Journal article
- Publication Details
- Genes chromosomes & cancer, Vol.56(4), pp.266-277
- Publisher
- United States
- DOI
- 10.1002/gcc.22432
- PMID
- 27910166
- ISSN
- 1045-2257
- eISSN
- 1098-2264
- Grant note
- P30 CA086862 / NCI NIH HHS
- Language
- English
- Date published
- 04/2017
- Academic Unit
- Pathology; Orthopedics and Rehabilitation
- Record Identifier
- 9984040399802771
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