4.3 Article

Antibody-Based Detection of ERG Rearrangement-Positive Prostate Cancer

Journal

NEOPLASIA
Volume 12, Issue 7, Pages 590-U95

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1593/neo.10726

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Funding

  1. National Cancer Institute (NCI) [CA125612]
  2. Early Detection Research Network [U01CA111275-06]
  3. Prostate Cancer Foundation [P50CA69568, R01CA132874]
  4. Doris Duke Charitable Foundation
  5. Burroughs Welcome Foundation
  6. Dana-Farber Harvard Cancer Center

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TMPRSS2-ERG gene fusions occur in 50% of prostate cancers and result in the overexpression of a chimeric fusion transcript that encodes a truncated ERG product. Previous attempts to detect truncated ERG products have been hindered by a lack of specific antibodies. Here, we characterize a rabbit anti-ERG monoclonal antibody (clone EPR 3864; Epitomics, Burlingame, CA) using immunoblot analysis on prostate cancer cell lines, synthetic TMPRSS2-ERG constructs, chromatin immunoprecipitation, and immunofluorescence. We correlated ERG protein expression with the presence of ERG gene rearrangements in prostate cancer tissues using a combined immunohistochemistry (IHC) and fluorescence in situ hybridization (FISH) analysis. We independently evaluated two patient cohorts and observed

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