DNA Methylation in Prostate Cancer: Clinical Implications and Potential Applications
ABSTRACT Background Prostate cancer is a common cancer with a variable prognosis. Its management is currently guided by histological and biological markers such as the Gleason score and PSA. Developments in molecular biology are now making it possible to identify new targets for better classificatio...
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Published in | Cancer medicine (Malden, MA) Vol. 14; no. 1; pp. e70528 - n/a |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
United States
John Wiley & Sons, Inc
01.01.2025
John Wiley and Sons Inc Wiley |
Subjects | |
Online Access | Get full text |
ISSN | 2045-7634 2045-7634 |
DOI | 10.1002/cam4.70528 |
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Summary: | ABSTRACT
Background
Prostate cancer is a common cancer with a variable prognosis. Its management is currently guided by histological and biological markers such as the Gleason score and PSA. Developments in molecular biology are now making it possible to identify new targets for better classification of prostate cancer. Among emerging biomarker, DNA methylation, an epigenetic process, is increasingly being studied in carcinogenesis. Techniques for analyzing DNA methylation are constantly improving, and digital PCR now allows absolute methylation quantification with high sensitivity. These techniques can be performed on circulating tumor DNA.
Materials & Methods
We conducted a literature review of scientific articles addressing the topic of DNA methylation in prostate cancer.
Results & discussion
This review summarizes the different genes whose methylation is involved in carcinogenesis and their clinical implications, both diagnostic and prognostic. Methylation monitoring could also be useful for the prediction of treatment response. However, most studies are retrospective, and prospective studies are needed to validate these data. |
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Bibliography: | The authors received no specific funding for this work. Funding ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Review-3 content type line 23 Funding: The authors received no specific funding for this work. |
ISSN: | 2045-7634 2045-7634 |
DOI: | 10.1002/cam4.70528 |