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Sequencing Small Non-coding RNA from Formalin-fixed Tissues and Serum-derived Exosomes from Castration-resistant Prostate Cancer Patients
Published on: November 19, 2019
Oncogenic role of engrailed-2 (en-2) in prostate cancer cell growth and survival
Sudeep K Bose1, Rebecca S Bullard, Carlton D Donald
1Department of Pathology and Laboratory Medicine, Medical University of South Carolina (MUSC), 165 Ashley Avenue, PO Box 250620, Charleston, SC-29425, U.S.A.
Abstract:
Prostate cancer is the second leading cause of cancer death among men in the United States of America. However, the molecular mechanisms underlying the disease remain largely unknown. Therefore, the identification of tumor specific molecules that serve as targets for the development of new cancer drugs is considered to be a major goal in cancer research. The mouse Engrailed-2 (En-2) gene, which is a homeobox-containing transcription factor was recently identified as a candidate oncogene in breast cancer. Here, we demonstrate that En-2 is over-expressed in human prostate cancer cells as compared to normal prostate epithelial cells. In addition, our data suggests that EN2 expression may be positively modulated by PAX2 transcription factor. Furthermore, down-regulation of EN2 expression by siRNA resulted in a decrease in PAX2 expression. We also provide evidence that down-regulation of EN2 expression causes a dramatic decrease in prostate cancer cell proliferation. Therefore, from our studies we conclude that En-2 is a candidate oncogene in prostate cancer and its PAX2-regulated expression contributes to prostate cancer cell growth.
Insights
Engrailed-2 (En-2) is over-expressed in prostate cancer, acting as an oncogene. Its regulation by PAX2 contributes to prostate cancer cell growth, offering a potential drug target.
Area of Science:
- Oncology
- Molecular Biology
- Gene Regulation
Background:
- Prostate cancer is a leading cause of male cancer deaths in the US.
- Molecular mechanisms of prostate cancer are not fully understood.
- Identifying tumor-specific molecules is crucial for developing targeted cancer therapies.
Purpose of the Study:
- To investigate the role of Engrailed-2 (En-2) as a candidate oncogene in human prostate cancer.
- To explore the relationship between En-2 and PAX2 transcription factor in prostate cancer cells.
Main Methods:
- Quantitative analysis of En-2 expression in human prostate cancer versus normal cells.
- Investigation of PAX2 modulation of EN2 expression.
- RNA interference (siRNA) to down-regulate EN2 expression and assess its impact on PAX2 levels and cell proliferation.
Main Results:
- En-2 is significantly over-expressed in human prostate cancer cells compared to normal prostate epithelial cells.
- PAX2 transcription factor positively modulates EN2 expression.
- Down-regulation of EN2 via siRNA leads to decreased PAX2 expression.
- Reducing EN2 expression dramatically inhibits prostate cancer cell proliferation.
Conclusions:
- En-2 functions as a candidate oncogene in prostate cancer.
- PAX2-regulated expression of En-2 contributes to prostate cancer cell growth.
- En-2 represents a potential therapeutic target for prostate cancer treatment.
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