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Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
The Great Potential of DNA Methylation in Triple-Negative Breast Cancer: From Biological Basics to Clinical
Wanying Xie1, Ying Wen1, Siqi Gong1
1Department of General Surgery, The Second Xiangya Hospital, Central South University, Changsha 410000, China.
Abstract:
Triple-negative breast cancer (TNBC), which is characterized by a lack of the estrogen receptor, the progesterone receptor, and HER2 expression, is the most aggressive breast cancer subtype and has a poor prognosis and high recurrence rates because of frequent chemotherapy resistance. As a crucial epigenetic regulator, DNA methylation modulates gene expression through aberrant methylation patterns, contributing to tumor progression and therapeutic resistance. Early diagnosis and treatment of TNBC are vital for its prognosis. The development of DNA methylation testing technology and the application of liquid biopsy provide technological support for early diagnosis and treatment. Additionally, preclinical and early-phase clinical studies suggest that epigenetic therapies targeting DNA methylation may hold promise for TNBC treatment, pending larger clinical trials. Furthermore, research on DNA methylation-based prognostic models enables personalized precision treatment for patients, helping to reduce unnecessary therapies and improve overall survival. The emerging role of DNA methylation patterns in predicting the therapeutic response and overcoming drug resistance is highlighted. In this narrative review, we integrate current research findings and clinical perspectives. We propose that DNA methylation presents promising research prospects for the diagnosis, treatment and prognosis prediction of TNBC. Future efforts should focus on translating methylation-driven insights into clinically actionable strategies, ultimately advancing precision oncology for this challenging disease.
Insights
DNA methylation plays a key role in triple-negative breast cancer (TNBC) progression and treatment resistance. Methylation testing and epigenetic therapies offer promising avenues for early diagnosis, personalized treatment, and improved outcomes in TNBC.
Area of Science:
- Epigenetics
- Oncology
- Genomics
Background:
- Triple-negative breast cancer (TNBC) is an aggressive subtype with poor prognosis due to chemotherapy resistance.
- DNA methylation, an epigenetic regulator, significantly influences gene expression and contributes to TNBC tumor progression and therapeutic resistance.
Purpose of the Study:
- To review current research on DNA methylation in TNBC.
- To explore the potential of DNA methylation in diagnosis, treatment, and prognosis prediction for TNBC.
- To highlight the role of DNA methylation in overcoming drug resistance and predicting therapeutic response.
Main Methods:
- Narrative review integrating current research findings and clinical perspectives.
- Analysis of preclinical and early-phase clinical studies on epigenetic therapies targeting DNA methylation in TNBC.
- Examination of DNA methylation testing technologies and liquid biopsy applications for TNBC diagnosis.
Main Results:
- Aberrant DNA methylation patterns are implicated in TNBC progression and resistance to chemotherapy.
- DNA methylation testing and liquid biopsy offer potential for early TNBC diagnosis and treatment.
- Epigenetic therapies targeting DNA methylation show promise for TNBC treatment.
- DNA methylation-based prognostic models can guide personalized precision treatment for TNBC patients.
Conclusions:
- DNA methylation presents significant research prospects for TNBC diagnosis, treatment, and prognosis.
- Translating methylation-driven insights into clinical strategies is crucial for advancing precision oncology in TNBC.
- Further research and clinical trials are needed to fully realize the potential of DNA methylation in managing TNBC.
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