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DNA Methylation as Drug Sensitivity Marker in RCC: A Systematic Review. | LitMetric

DNA Methylation as Drug Sensitivity Marker in RCC: A Systematic Review.

Epigenomes

First Department of Urology, School of Medicine, Faculty of Health Sciences, Aristotle University of Thessaloniki, 541 24 Thessaloniki, Greece.

Published: July 2024

AI Article Synopsis

  • - Patient responses to systemic treatments for renal cell cancer (RCC) are often poor and inconsistent, highlighting the need for better predictive tools for therapy sensitivity.
  • - This study systematically reviewed 31 articles examining how promoter methylation status relates to patient or cell line responses to systemic agents in RCC.
  • - While the majority of studies indicated a potential link between methylation patterns and treatment response, the evidence remains inconclusive, suggesting further research is necessary to establish robust correlations.

Article Abstract

Patient response after treatment of renal cell cancer (RCC) with systemic agents, which include various drug categories, is generally poor and unpredictable. In this context, the ideal drug administration includes tools to predict the sensitivity of the disease to therapy. The aim of this study was to systematically summarize the reports on the predictive value of the methylation status in the systemic therapy of RCC. Only original articles reporting on the association of promoter methylation with the response of patients or cell lines to systemic agents were included in this review. We applied PRISMA recommendations to the structure and methodology of this systematic review. Our literature search concluded with 31 articles conducted on RCC cell lines and patient tissues. The majority of the studies demonstrated a methylation-dependent response to systemic agents. This correlation suggests that the methylation pattern can be used as a predictive tool in the management of RCC with various classes of systemic agents. However, although methylation biomarkers show promise for predicting response, the evidence of such correlation is still weak. More studies on the gene methylation pattern in patients under systemic therapy and its correlation with different degrees of response are needed.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11270435PMC
http://dx.doi.org/10.3390/epigenomes8030028DOI Listing

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