Related Experiment Video
Updated: Jun 20, 2026

MicroRNA Detection in Prostate Tumors by Quantitative Real-time PCR (qPCR)
Published on: May 16, 2012
TMPRSS2-ERG gene fusion status in minute (minimal) prostatic adenocarcinoma
Roula Albadine1, Mathieu Latour, Antoun Toubaji
1Department of Pathology, The Johns Hopkins Medical Institutions, Baltimore, Maryland, USA.
Abstract:
Minute prostatic adenocarcinomas are considered to be of insufficient virulence. Given recent suggestions of TMPRSS2-ERG gene fusion association with aggressive prostatic adenocarcinoma, we evaluated the incidence of TMPRSS2-ERG fusion in minute prostatic adenocarcinomas. A total of 45 consecutive prostatectomies with minute adenocarcinoma were used for tissue microarray construction. A total of 63 consecutive non-minimal, Gleason Score 6 tumors, from a separate PSA Era prostatectomy tissue microarray, were used for comparison. FISH was carried out using ERG break-apart probes. Tumors were assessed for fusion by deletion (Edel) or split (Esplit), duplicated fusions and low-level copy number gain in normal ERG gene locus. Minute adenocarcinomas: Fusion was evaluable in 32/45 tumors (71%). Fifteen out of 32 (47%) tumors were positive for fusion. Six (19%) were of the Edel class and 7 (22%) were classified as combined Edel+Esplit. Non-minute adenocarcinomas (pT2): Fusion was identified in 20/30 tumors (67%). Four (13%) were of Edel class and 5 (17%) were combined Edel+Esplit. Duplicated fusions were encountered in 5 (16%) tumors. Non-minute adenocarcinomas (pT3): Fusion was identified in 19/33 (58%). Fusion was due to a deletion in 6 (18%) tumors. Seven tumors (21%) were classified as combined Edel+Esplit. One tumor showed Esplit alone. Duplicated fusions were encountered in 3 (9%) cases. The incidence of duplicated fusions was higher in non-minute adenocarcinomas (13 vs 0%; P=0.03). A trend for higher incidence of low-level copy number gain in normal ERG gene locus without fusion was noted in non-minute adenocarcinomas (10 vs 0%; P=0.07). We found a TMPRSS2-ERG fusion rate of 47% in minute adenocarcinomas. The latter is not significantly different from that of grade matched non-minute adenocarcinomas. The incidence of duplicated fusion was higher in non-minute adenocarcinomas. Our finding of comparable rate of TMPRSS2-ERG fusion in minute adenocarcinomas may argue against its value as a marker of aggressive prostate carcinoma phenotype.
Insights
Minute prostate adenocarcinomas show a 47% TMPRSS2-ERG gene fusion rate, similar to non-minute tumors. This finding suggests the TMPRSS2-ERG fusion may not reliably indicate aggressive prostate cancer.
Area of Science:
- Urology
- Oncology
- Molecular Biology
Background:
- Minute prostatic adenocarcinomas are typically considered low-virulence.
- The TMPRSS2-ERG gene fusion has been linked to aggressive prostate adenocarcinoma.
- Evaluating this fusion in minute adenocarcinomas is crucial for understanding prostate cancer behavior.
Purpose of the Study:
- To determine the incidence of TMPRSS2-ERG gene fusion in minute prostatic adenocarcinomas.
- To compare the fusion rates between minute and non-minute adenocarcinomas.
- To assess the potential of TMPRSS2-ERG fusion as a marker for aggressive prostate cancer phenotypes.
Main Methods:
- Tissue microarray construction from 45 minute adenocarcinomas and 63 non-minimal, Gleason Score 6 tumors.
- Fluorescence in situ hybridization (FISH) using ERG break-apart probes.
- Assessment for fusion by deletion (Edel), split (Esplit), duplicated fusions, and low-level copy number gain.
Main Results:
- TMPRSS2-ERG fusion was detected in 47% of minute adenocarcinomas (15/32).
- Fusion rates in minute adenocarcinomas were comparable to grade-matched non-minute adenocarcinomas (pT2 and pT3).
- Duplicated fusions were more frequent in non-minute adenocarcinomas (13% vs 0%, P=0.03).
Conclusions:
- The incidence of TMPRSS2-ERG fusion in minute adenocarcinomas is similar to that in non-minute adenocarcinomas.
- The presence of TMPRSS2-ERG fusion may not be a reliable indicator of aggressive prostate cancer phenotype in minute tumors.
- Further research is needed to understand the prognostic implications of TMPRSS2-ERG fusion in early-stage prostate cancer.
More Related Videos
09:49Oncogenic Gene Fusion Detection Using Anchored Multiplex Polymerase Chain Reaction Followed by Next Generation Sequencing
Published on: July 5, 2019
09:37Defining Gene Functions in Tumorigenesis by Ex vivo Ablation of Floxed Alleles in Malignant Peripheral Nerve Sheath Tumor Cells
Published on: August 25, 2021
Related Concept Videos
Abnormal Proliferation
The Ras Gene
Ras is a superfamily...