Recurrent Fusion of TMPRSS2 and ETS Transcription Factor Genes in Prostate Cancer

Author:

Tomlins Scott A.12345,Rhodes Daniel R.12345,Perner Sven12345,Dhanasekaran Saravana M.12345,Mehra Rohit12345,Sun Xiao-Wei12345,Varambally Sooryanarayana12345,Cao Xuhong12345,Tchinda Joelle12345,Kuefer Rainer12345,Lee Charles12345,Montie James E.12345,Shah Rajal B.12345,Pienta Kenneth J.12345,Rubin Mark A.12345,Chinnaiyan Arul M.12345

Affiliation:

1. Department of Pathology, University of Michigan Medical School, 1301 Catherine Street, Ann Arbor, MI 48109–0602, USA.

2. Bioinformatics Program, University of Michigan Medical School, 1301 Catherine Street, Ann Arbor, MI 48109–0602, USA.

3. Department of Urology, University of Michigan Medical School, 1301 Catherine Street, Ann Arbor, MI 48109–0602, USA.

4. Department of Internal Medicine, University of Michigan Medical School, 1301 Catherine Street, Ann Arbor, MI 48109–0602, USA.

5. Michigan Urology Center, University of Michigan Medical School, 1301 Catherine Street, Ann Arbor, MI 48109–0602, USA.

Abstract

Recurrent chromosomal rearrangements have not been well characterized in common carcinomas. We used a bioinformatics approach to discover candidate oncogenic chromosomal aberrations on the basis of outlier gene expression. Two ETS transcription factors, ERG and ETV1 , were identified as outliers in prostate cancer. We identified recurrent gene fusions of the 5′ untranslated region of TMPRSS2 to ERG or ETV1 in prostate cancer tissues with outlier expression. By using fluorescence in situ hybridization, we demonstrated that 23 of 29 prostate cancer samples harbor rearrangements in ERG or ETV1 . Cell line experiments suggest that the androgen-responsive promoter elements of TMPRSS2 mediate the overexpression of ETS family members in prostate cancer. These results have implications in the development of carcinomas and the molecular diagnosis and treatment of prostate cancer.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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