Identification of a Disease-Defining Gene Fusion in Epithelioid Hemangioendothelioma

Munir R. Tanas(Cleveland Clinic), Andrea Sboner(Yale University), André M. Oliveira(Mayo Clinic), Michele R. Erickson‐Johnson(Mayo Clinic), Jessica Hespelt(Cleveland Clinic), Philip J. Hanwright(Cleveland Clinic), John J. Flanagan(Advanced Cell Diagnostics (United States)), Yuling Luo(Advanced Cell Diagnostics (United States)), Kerry Fenwick(Institute of Cancer Research), Rachael Natrajan(Institute of Cancer Research), Costas Mitsopoulos(Institute of Cancer Research), Marketa Zvelebil(Institute of Cancer Research), Benjamin Hoch(University of Washington), Sharon W. Weiss(Emory University), Maria Dêbiec‐Rychter(KU Leuven), Raf Sciot(KU Leuven), Robert B. West(Stanford Medicine), Alexander J. Lazar(The University of Texas MD Anderson Cancer Center), Alan Ashworth(Institute of Cancer Research), Jorge S. Reis‐Filho(Institute of Cancer Research), Christopher J. Lord(Institute of Cancer Research), Mark Gerstein(Yale University), Mark A. Rubin(Cornell University), Brian P. Rubin(Cleveland Clinic)
Science Translational Medicine
August 31, 2011
Cited by 401

Abstract

Integrating transcriptomic sequencing with conventional cytogenetics, we identified WWTR1 (WW domain-containing transcription regulator 1) (3q25) and CAMTA1 (calmodulin-binding transcription activator 1) (1p36) as the two genes involved in the t(1;3)(p36;q25) chromosomal translocation that is characteristic of epithelioid hemangioendothelioma (EHE), a vascular sarcoma. This WWTR1/CAMTA1 gene fusion is under the transcriptional control of the WWTR1 promoter and encodes a putative chimeric transcription factor that joins the amino terminus of WWTR1, a protein that is highly expressed in endothelial cells, in-frame to the carboxyl terminus of CAMTA1, a protein that is normally expressed only in brain. Thus, CAMTA1 expression is activated inappropriately through a promoter-switch mechanism. The gene fusion is present in virtually all EHEs tested but is absent from all other vascular neoplasms, demonstrating it to be a disease-defining genetic alteration. A sensitive and specific break-apart fluorescence in situ hybridization assay was also developed to detect the translocation and will assist in the evaluation of this diagnostically challenging neoplasm. The chimeric WWTR1/CAMTA1 transcription factor may represent a therapeutic target for EHE and offers the opportunity to shed light on the functions of two poorly characterized proteins.


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