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Published on: April 28, 2021
Targeting the DNA repair pathway for breast cancer therapy: Beyond the molecular subtypes
Yuting Qu1, Sisi Qin2, Zhihui Yang1
1Zunyi Medical University, No.6 Xuefu West Road, Zunyi, Guizhou Province, 563006, China; Department of Breast Surgery, Guizhou Provincial People's Hospital, NO.83 Zhongshan East Road, Guiyang, Guizhou Province 550002, China.
Abstract:
DNA repair is a vital mechanism in cells that protects against DNA damage caused by internal and external factors. It involves a network of signaling pathways that monitor and transmit damage signals, activating various cellular activities to repair DNA damage and maintain genomic integrity. Dysfunctions in this repair pathway are strongly associated with the development and progression of cancer. However, they also present an opportunity for targeted therapy in breast cancer. Extensive research has focused on developing inhibitors that play a crucial role in the signaling pathway of DNA repair, particularly due to the remarkable success of PARP1 inhibitors (PARPis) in treating breast cancer patients with BRCA1/2 mutations. In this review, we summarize the current research progress and clinical implementation of BRCA and BRCAness in targeted treatments for the DNA repair pathway. Additionally, we present advancements in diverse inhibitors of DNA repair, both as individual and combined approaches, for treating breast cancer. We also discuss the clinical application of DNA repair-targeted therapy for breast cancer, including the rationale, indications, and summarized clinical data for patients with different breast cancer subtypes. We assess their influence on cancer progression, survival rates, and major adverse reactions. Last, we anticipate forthcoming advancements in targeted therapy for cancer treatment and emphasize prospective areas of development.
Insights
DNA repair pathways are crucial for genomic integrity and cancer development. Targeting these pathways, especially with PARP1 inhibitors (PARPis) in BRCA-mutated breast cancer, offers new therapeutic strategies.
Area of Science:
- Molecular Biology
- Genomic Stability
- Cancer Therapeutics
Background:
- DNA repair mechanisms protect cells from damage, maintaining genomic integrity.
- Defects in DNA repair pathways are linked to cancer development and progression.
- These defects also represent therapeutic vulnerabilities, particularly in breast cancer.
Purpose of the Study:
- To review current research and clinical applications of targeting DNA repair pathways in breast cancer.
- To summarize advancements in DNA repair inhibitors and their combination therapies.
- To discuss the clinical utility, outcomes, and adverse effects of DNA repair-targeted therapies for breast cancer.
Main Methods:
- Literature review of research on BRCA, BRCAness, and DNA repair inhibitors.
- Analysis of clinical data for various breast cancer subtypes treated with DNA repair-targeted therapies.
- Assessment of treatment efficacy, survival rates, and adverse events.
Main Results:
- PARP1 inhibitors show significant success in BRCA-mutated breast cancer.
- Diverse DNA repair inhibitors are advancing as monotherapies and combination treatments.
- Clinical data supports the application of DNA repair-targeted therapy across different breast cancer subtypes.
Conclusions:
- Targeting DNA repair pathways, including BRCA and BRCAness, is a promising strategy for breast cancer treatment.
- Further advancements in inhibitors and combination therapies are expected.
- Understanding clinical applications and outcomes is vital for optimizing patient care.
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