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MicroRNA Detection in Prostate Tumors by Quantitative Real-time PCR qPCR
Published on: May 16, 2012
The Germ Cell Gene TDRD1 as an ERG Target Gene and a Novel Prostate Cancer Biomarker
Lijuan Xiao1, Rainer B Lanz2, Anna Frolov3
1Departments of Medicine-Hematology and Oncology, Baylor College of Medicine, Houston, Texas.
Background:
TMPRSS2-ERG fusion occurs in about half of prostate cancers and results in over-expression of the oncogenic ERG protein in the prostate. The mechanism by which ERG contributes to prostate cancer initiation and progression remains largely unknown. Because ERG is a transcriptional activator, we reasoned that the target genes regulated by ERG could contribute to prostate cancer development.
Methods:
In a search for ERG target genes, we took advantage of published datasets from the MSKCC Prostate Oncogene Project, in which a comprehensive analysis was applied to define transcriptomes in 150 prostate tumors. We retrieved the mRNA expression dataset, split them based on ERG expression, and identified genes whose expression levels are associated with ERG mRNA levels.
Results:
mRNA expression levels of 21 genes were found to be significantly increased, while for one gene it was decreased in ERG-positive prostate tumors. Among them, the expression of TDRD1 was the most significantly increased in ERG-positive tumors. Among 131 primary prostate tumors which were primarily from European American patients, TDRD1 is over-expressed in 68% of samples, while ERG is overexpressed in 48% of samples, suggesting an additional ERG-independent mechanism of TDRD1 overexpression. In African American prostate tumors, TDRD1 mRNA is expressed in 44%, while ERG is expressed in 24% of samples. In normal tissues, TDRD1 mRNA is exclusively expressed in germ cells and its protein is also known as cancer/testis antigen 41.1 (CT41.1). We generated a mouse monoclonal antibody that recognizes human TDRD1 protein with high specificity and sensitivity. By Western blot analysis and immunohistochemistry (IHC) staining, we demonstrate that TDRD1 protein is expressed in the majority of human prostate tumors, but not in normal prostate tissue. Finally, TDRD1 is not induced in the prostate of ERG overexpression transgenic mice, suggesting that such model does not fully recapitulate the TMPRSS2/ERG fusion-dependent human prostate cancer development.
Conclusions:
Our results suggest TDRD1 as a novel prostate cancer biomarker. As an ERG target gene, TDRD1 might play an important role in human prostate cancer development, and as a cancer/testis antigen, TDRD1 might have long-term potential to be a therapeutic target for prostate cancer immunotherapy. Prostate 76:1271-1284, 2016. © 2016 Wiley Periodicals, Inc.
Insights
This study identifies TDRD1 as a novel prostate cancer biomarker and potential therapeutic target. TDRD1 is overexpressed in prostate tumors and may play a role in cancer development.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Prostate cancer is often driven by TMPRSS2-ERG fusion, leading to ERG oncogene overexpression.
- The precise mechanisms by which ERG drives prostate cancer initiation and progression are not fully understood.
- ERG is a transcriptional activator, suggesting its target genes are key to prostate cancer development.
Purpose of the Study:
- To identify ERG target genes involved in prostate cancer development.
- To investigate the role of TDRD1 in prostate cancer.
Main Methods:
- Analysis of publicly available transcriptomic datasets from 150 prostate tumors (MSKCC Prostate Oncogene Project).
- Comparison of gene expression profiles between ERG-positive and ERG-negative prostate tumors.
- Validation of TDRD1 expression in prostate tumors using Western blot and immunohistochemistry (IHC).
Main Results:
- TDRD1 expression was significantly increased in ERG-positive prostate tumors.
- TDRD1 is overexpressed in 68% of European American and 44% of African American prostate tumors, indicating ERG-independent mechanisms.
- TDRD1 protein is detected in most prostate tumors but not in normal prostate tissue; it is also identified as a cancer/testis antigen (CT41.1).
Conclusions:
- TDRD1 is a promising novel biomarker for prostate cancer.
- TDRD1's role as an ERG target gene suggests its involvement in prostate cancer pathogenesis.
- TDRD1's cancer/testis antigen status presents potential for prostate cancer immunotherapy.

