POU2AF3‐rearranged sarcomas: A novel tumor defined by fusions of EWSR1 or FUS to a gene formerly designated COLCA2

Author:

Hiemenz Matthew C.1,Kaur Jaspreet1,Kuang Zheng1ORCID,Huang Richard S. P.1,Harries Lukas1,Metzger Dana1,Schiavone Kelsie1,Millis Sherri Z.1,Lin Douglas I.1,Lechpammer Mirna1,Decker Brennan1,Mata Douglas A.1ORCID,Reddy Abhinav1,Parke Matthew2,Lee Eun Y.3,Cui Xiaoyan4,Iwenofu O. Hans4ORCID,Buehler Darya5,Henderson Les6,Baldwin Erin M.6,Boikos Sosipatros A.7,Ramkissoon Shakti H.18,Smith Steven C.9ORCID

Affiliation:

1. Foundation Medicine Cambridge Massachusetts USA

2. Department of Pathology University of Arkansas for Medical Sciences Little Rock Arkansas USA

3. Department of Pathology and Laboratory Medicine University of Kentucky Lexington Kentucky USA

4. Department of Pathology and Laboratory Medicine The Ohio State University Wexner Medical Center Columbus Ohio USA

5. Department of Pathology and Laboratory Medicine University of Wisconsin School of Medicine and Public Health Madison Wisconsin USA

6. Wisconsin State Laboratory of Hygiene University of Wisconsin‐Madison Madison Wisconsin USA

7. Department of Hematology and Oncology Georgetown Lombardi Comprehensive Cancer Center Washington DC USA

8. Department of Pathology Wake Forest School of Medicine and Wake Forest Comprehensive Cancer Center Winston‐Salem North Carolina USA

9. Departments of Pathology and Surgery and Massey Cancer Center Virginia Commonwealth University School of Medicine Richmond Virginia USA

Abstract

AbstractGene fusions involving EWSR1 or FUS as the 5′ partner have been reported in a diverse array of sarcomas. Here, we characterize the histopathology and genomics of six tumors harboring a gene fusion between EWSR1 or FUS and POU2AF3, an understudied, putative colorectal cancer predisposition gene. Striking morphologic features reminiscent of synovial sarcoma were observed including a biphasic appearance with variable fusiform to epithelioid cytomorphology and staghorn‐type vasculature. RNA sequencing demonstrated variable breakpoints in EWSR1/FUS along with similar breakpoints in POU2AF3 that encompassed a 3′ portion of this gene. For cases in which additional information was available, the behavior of these neoplasms was aggressive with local spread and/or distant metastases. Although further studies are needed to confirm the functional significance of our findings, POU2AF3 fusions to EWSR1 or FUS may define a novel type of POU2AF3‐rearranged sarcomas with aggressive, malignant behavior.

Publisher

Wiley

Subject

Cancer Research,Genetics

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