V-ets erythroblastosis virus E26 oncogene homolog (avian)/Trefoil factor 3/high-molecular-weight cytokeratin triple immunostain: a novel tissue-based biomarker in prostate cancer with potential clinical application.

TitleV-ets erythroblastosis virus E26 oncogene homolog (avian)/Trefoil factor 3/high-molecular-weight cytokeratin triple immunostain: a novel tissue-based biomarker in prostate cancer with potential clinical application.
Publication TypeJournal Article
Year of Publication2013
AuthorsPark K, Chiu Y-L, Rubin MA, Demichelis F, Mosquera JMiguel
JournalHum Pathol
Volume44
Issue10
Pagination2282-92
Date Published2013 Oct
ISSN1532-8392
KeywordsAdenocarcinoma, Adult, Aged, Biomarkers, Tumor, Humans, Keratins, Male, Middle Aged, Molecular Weight, Peptides, Prostatic Neoplasms, Tissue Array Analysis, Trans-Activators, Transcriptional Regulator ERG, Trefoil Factor-3
Abstract

Trefoil factor 3 (TFF3) is associated with various cancers and overexpressed in a subset of prostate cancers. Functional studies suggest that v-ets erythroblastosis virus E26 oncogene homolog (avian) (ERG) down-regulates TFF3 expression in hormone-naïve prostate cancer. To characterize this inverse relationship, we developed a triple immunostain encompassing ERG, TFF3, and high-molecular-weight cytokeratin. Triple stain was performed on 96 tumors and 52 benign cases represented in tissue microarrays. Distinct ERG and TFF3 protein was expressed in 45% (43/96) and 36% (35/96) of prostate cancers, respectively. Coexpression was observed in 5% (5/96) of tumor cases, and 24% (23/96) did not express ERG or TFF3. The inverse expression of ERG and TFF3 was significant (P < .0001), with 57% (30/53) of ERG-negative tumors demonstrating TFF3 expression. Sensitivity and specificity of combined ERG and TFF3 expression in detecting prostate cancer were 76% and 96%, respectively. The feasibility of triple immunostain protocol was validated in a set of 76 needle biopsies. The application of this multiplex in situ biomarker for molecular characterization of prostate cancer and as a supplemental diagnostic and prognostic tool in prostate needle biopsies should be further explored.

DOI10.1016/j.humpath.2013.05.010
Alternate JournalHum Pathol
PubMed ID23856515
Grant List5U01 CA11275-07 / CA / NCI NIH HHS / United States
Related Faculty: 
Juan Miguel Mosquera, M.D.

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