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Updated: Sep 21, 2025

Continuous Fluorescence-Based Endonuclease-Coupled DNA Methylation Assay to Screen for DNA Methyltransferase Inhibitors
Published on: August 5, 2022
DNMT3A and DNMT3B in Breast Tumorigenesis and Potential Therapy
Xiaxia Man1, Qi Li2, Baogang Wang3
1Department of Oncologic Gynecology, the First Hospital of Jilin University, Jilin, China.
Abstract:
Breast cancer has become a leading cause of cancer-related deaths in women worldwide. DNA methylation has been revealed to play an enormously important role in the development and progression of breast cancer. DNA methylation is regulated by DNA methyltransferases (DNMTs), including DNMT1, DNMT2, and DNMT3. DNMT3 family has three members: DNMT3A, DNMT3B, and DNMT3L. The roles and functions of DNMT1 in breast cancer have been well reviewed. In this article, the roles of DNMT3A and DNMT3B in breast tumorigenesis and development are reviewed. We also discuss the SNP and mutations of DNMT3A and DNMT3B in breast cancer. In addition, we summarize how DNMT3A and DNMT3B are regulated by non-coding RNAs and signaling pathways in breast cancer, and targeting the expression levels of DNMT3A and DNMT3B may be a promising therapeutic approach for breast cancer. This review will provide reference for further studies on the biological functions and molecular mechanisms of DNMT3A and DNMT3B in breast cancer.
Insights
DNA methyltransferases (DNMT3A and DNMT3B) are crucial in breast cancer development. Targeting these enzymes offers a promising therapeutic strategy for breast cancer treatment.
Area of Science:
- Oncology
- Epigenetics
- Molecular Biology
Background:
- Breast cancer is a major cause of cancer deaths in women globally.
- DNA methylation, regulated by DNA methyltransferases (DNMTs), is vital in breast cancer progression.
- While DNMT1's role is known, DNMT3A and DNMT3B roles require further review.
Purpose of the Study:
- To review the roles of DNMT3A and DNMT3B in breast tumorigenesis and development.
- To discuss single nucleotide polymorphisms (SNPs) and mutations of DNMT3A and DNMT3B in breast cancer.
- To summarize regulatory mechanisms of DNMT3A and DNMT3B by non-coding RNAs and signaling pathways.
Main Methods:
- Literature review of existing studies on DNMT3A and DNMT3B in breast cancer.
- Analysis of data regarding SNPs and mutations.
- Synthesis of information on regulatory pathways and therapeutic targeting.
Main Results:
- DNMT3A and DNMT3B are implicated in breast cancer initiation and progression.
- SNPs and mutations in DNMT3A and DNMT3B are associated with breast cancer.
- Non-coding RNAs and signaling pathways significantly regulate DNMT3A and DNMT3B expression.
Conclusions:
- DNMT3A and DNMT3B are critical players in breast cancer.
- Understanding their regulation provides insights into molecular mechanisms.
- Targeting DNMT3A and DNMT3B presents a potential therapeutic avenue for breast cancer.
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