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Updated: May 24, 2026

Methyl-binding DNA capture Sequencing for Patient Tissues
Published on: October 31, 2016
DNA methylation in promoter region as biomarkers in prostate cancer
1Division of Cancer Prevention and Controls, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Abstract:
The prostate gland is the most common site of cancer and the second leading cause of cancer death in American men. Recent emerging molecular biological technologies help us to know that epigenetic alterations such as DNA methylation within the regulatory (promoter) regions of genes are associated with transcriptional silencing in cancer. Promoter hypermethylation of critical pathway genes could be potential biomarkers and therapeutic targets for prostate cancer. In this chapter, we updated current information on methylated genes associated with the development and progression of prostate cancer. Over 40 genes have been investigated for methylation in promoter region in prostate cancer. These methylated genes are involved in critical pathways, such as DNA repair, metabolism, and invasion/metastasis. The role of hypermethylated genes in regulation of critical pathways in prostate cancer is discussed. These findings may provide new information of the pathogenesis, the exciting potential to be predictive and to provide personalized treatment of prostate cancer. Indeed, some epigenetic alterations in prostate tumors are being translated into clinical practice for therapeutic use.
Insights
Epigenetic alterations, specifically DNA methylation in gene promoter regions, are linked to prostate cancer development and progression. These changes offer potential biomarkers and therapeutic targets for personalized prostate cancer treatment.
Area of Science:
- Oncology
- Molecular Biology
- Epigenetics
Background:
- Prostate cancer is a leading cause of cancer death in American men.
- Epigenetic alterations, including DNA methylation, are implicated in cancer development.
- Gene promoter hypermethylation can lead to transcriptional silencing in cancer cells.
Purpose of the Study:
- To review current knowledge on methylated genes in prostate cancer.
- To explore the role of these methylated genes in critical cellular pathways.
- To highlight the potential of epigenetic alterations as biomarkers and therapeutic targets.
Main Methods:
- Review of scientific literature on gene promoter methylation in prostate cancer.
- Analysis of over 40 investigated methylated genes.
- Discussion of the involvement of these genes in DNA repair, metabolism, and invasion/metastasis pathways.
Main Results:
- Over 40 genes have been identified with promoter hypermethylation in prostate cancer.
- These methylated genes are involved in key pathways crucial for cancer progression.
- Hypermethylation plays a significant role in regulating these critical pathways.
Conclusions:
- Methylated genes in prostate cancer offer insights into pathogenesis.
- Epigenetic alterations show potential as predictive biomarkers for personalized treatment.
- Some epigenetic modifications are already being integrated into clinical practice for prostate cancer therapy.
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