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Updated: Jul 29, 2025

Continuous Fluorescence-Based Endonuclease-Coupled DNA Methylation Assay to Screen for DNA Methyltransferase Inhibitors
Published on: August 5, 2022
Crosstalk between miRNAs and DNA Methylation in Cancer
Michela Saviana1, Patricia Le1, Lavender Micalo1
1Department of Internal Medicine, Division of Pulmonary Diseases and Critical Care Medicine, Virginia Commonwealth University, 1250 E. Marshall Street, Richmond, VA 23298, USA.
Abstract:
miRNAs are some of the most well-characterized regulators of gene expression. Integral to several physiological processes, their aberrant expression often drives the pathogenesis of both benign and malignant diseases. Similarly, DNA methylation represents an epigenetic modification influencing transcription and playing a critical role in silencing numerous genes. The silencing of tumor suppressor genes through DNA methylation has been reported in many types of cancer and is associated with tumor development and progression. A growing body of literature has described the crosstalk between DNA methylation and miRNAs as an additional layer in the regulation of gene expression. Methylation in miRNA promoter regions inhibits its transcription, while miRNAs can target transcripts and subsequently regulate the proteins responsible for DNA methylation. Such relationships between miRNA and DNA methylation serve an important regulatory role in several tumor types and highlight a novel avenue for potential therapeutic targets. In this review, we discuss the crosstalk between DNA methylation and miRNA expression in the pathogenesis of cancer and describe how miRNAs influence DNA methylation and, conversely, how methylation impacts the expression of miRNAs. Finally, we address how these epigenetic modifications may be leveraged as biomarkers in cancer.
Insights
DNA methylation and microRNAs (miRNAs) are key epigenetic regulators. Their interplay influences gene expression and cancer development, offering potential therapeutic and biomarker strategies.
Area of Science:
- Epigenetics
- Molecular Biology
- Cancer Research
Background:
- MicroRNAs (miRNAs) are crucial gene expression regulators involved in physiological processes and disease pathogenesis.
- DNA methylation is an epigenetic modification critical for gene silencing, particularly tumor suppressor genes in cancer.
- Aberrant epigenetic modifications, including DNA methylation and miRNA dysregulation, are implicated in cancer development and progression.
Purpose of the Study:
- To review the intricate crosstalk between DNA methylation and miRNA expression in cancer pathogenesis.
- To elucidate the mechanisms by which miRNAs influence DNA methylation and vice versa.
- To explore the potential of these epigenetic modifications as cancer biomarkers and therapeutic targets.
Main Methods:
- Literature review of studies investigating the relationship between DNA methylation and miRNA expression in cancer.
- Analysis of molecular mechanisms underlying miRNA promoter methylation and miRNA-mediated regulation of DNA methylation machinery.
- Synthesis of evidence on the role of this epigenetic crosstalk in various tumor types.
Main Results:
- DNA methylation in miRNA promoter regions can inhibit miRNA transcription.
- miRNAs can target transcripts encoding proteins involved in DNA methylation, thus regulating the epigenome.
- This reciprocal regulation plays a significant role in the pathogenesis of multiple cancer types.
- The interplay between DNA methylation and miRNAs represents a complex regulatory network in cancer.
Conclusions:
- The crosstalk between DNA methylation and miRNAs is a critical layer of gene regulation in cancer.
- Understanding this epigenetic interplay is essential for developing novel cancer diagnostics and therapeutics.
- Targeting these epigenetic modifications holds promise for future cancer treatment strategies.
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