Targeting Cellular DNA Damage Response in Cancer and Bacterial Infections: Current Progress, Challenges, and Opportunities

Review Targeting Cellular DNA Damage Response in Cancer and Bacterial Infections: Current Progress, Challenges, and Opportunities Ranxun Lin 1, Xu Zhang 1, Qinwei Zhu 1, Xuening Chen 1, Lin Dai 1, Longheng Li 1, Zuoan Li 2, and Zhonghui Lin 1,* 1 College of Chemistry, Fuzhou University, Fuzhou 350108, China 2 Shengli Clinical Medical College of Fujian Medical University, Department of Emergency, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fujian Provincial Key Laboratory of Emergency Medicine, Fuzhou 350108, China * Correspondence: [email protected] Received: 20 November 2024; Revised: 30 December 2024; Accepted: 21 February 2025; Published: 3 April 2025 Abstract: Effective cancer treatment remains challenging due to the genomic instability of tumors and the frequent emergence of resistance. Traditional approaches such as radiotherapy, chemotherapy, and immunotherapy face limitations in addressing tumor heterogeneity and resistance mechanisms. Targeting the DNA damage response (DDR) pathway has emerged as an innovative strategy, either as monotherapy or in combination with conventional treatments. DDR-targeted therapies, including poly-ADP-ribose polymerase (PARP) inhibitors, have shown promise in reducing tumor growth and enhancing patient outcomes. Emerging targets such as ATM, ATR, CHK1/2, WRN, and PARG, coupled with cutting-edge technologies like CRISPR and proteolysis-targeting chimeras (PROTACs), have opened new avenues for precise and effective cancer treatment. Furthermore, combining DDR inhibitors with established therapies, such as immune checkpoint inhibitors, has demonstrated synergistic benefits, improving therapeutic efficacy and overcoming resistance. Beyond cancer, DDR inhibitors also offer the potential to combat bacterial pathogens by exploiting vulnerabilities in microbial DNA repair systems. This review focuses on the major advantages, challenges, and future directions of DDR-targeted therapies in cancer and bacterial infections. We also discuss the integration of these therapies with traditional approaches, highlighting their potential to enhance therapeutic outcomes across diverse applications.

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Journal
Health and Metabolism
Published
2025-04-03
DOI
https://doi.org/10.53941/hm.2025.100010
Primary Topic
DNA Repair Mechanisms
Type
article
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0.00
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article

Targeting Cellular DNA Damage Response in Cancer and Bacterial Infections: Current Progress, Challenges, and Opportunities

Xuening Chen, Rongbo Lin, Zuoan Li, L.Y Li et al.
Health and Metabolism
DNA Repair Mechanisms
article

Targeting Cellular DNA Damage Response in Cancer and Bacterial Infections: Current Progress, Challenges, and Opportunities

Xuening Chen, Rongbo Lin, Zuoan Li, L.Y Li, Zhonghui Lin, Xu Zhang, Qinwei Zhu, Lin Dai
article en

Abstract

Review Targeting Cellular DNA Damage Response in Cancer and Bacterial Infections: Current Progress, Challenges, and Opportunities Ranxun Lin 1, Xu Zhang 1, Qinwei Zhu 1, Xuening Chen 1, Lin Dai 1, Longheng Li 1, Zuoan Li 2, and Zhonghui Lin 1,* 1 College of Chemistry, Fuzhou University, Fuzhou 350108, China 2 Shengli Clinical Medical College of Fujian Medical University, Department of Emergency, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fujian Provincial Key Laboratory of Emergency Medicine, Fuzhou 350108, China * Correspondence: [email protected] Received: 20 November 2024; Revised: 30 December 2024; Accepted: 21 February 2025; Published: 3 April 2025 Abstract: Effective cancer treatment remains challenging due to the genomic instability of tumors and the frequent emergence of resistance. Traditional approaches such as radiotherapy, chemotherapy, and immunotherapy face limitations in addressing tumor heterogeneity and resistance mechanisms. Targeting the DNA damage response (DDR) pathway has emerged as an innovative strategy, either as monotherapy or in combination with conventional treatments. DDR-targeted therapies, including poly-ADP-ribose polymerase (PARP) inhibitors, have shown promise in reducing tumor growth and enhancing patient outcomes. Emerging targets such as ATM, ATR, CHK1/2, WRN, and PARG, coupled with cutting-edge technologies like CRISPR and proteolysis-targeting chimeras (PROTACs), have opened new avenues for precise and effective cancer treatment. Furthermore, combining DDR inhibitors with established therapies, such as immune checkpoint inhibitors, has demonstrated synergistic benefits, improving therapeutic efficacy and overcoming resistance. Beyond cancer, DDR inhibitors also offer the potential to combat bacterial pathogens by exploiting vulnerabilities in microbial DNA repair systems. This review focuses on the major advantages, challenges, and future directions of DDR-targeted therapies in cancer and bacterial infections. We also discuss the integration of these therapies with traditional approaches, highlighting their potential to enhance therapeutic outcomes across diverse applications.

Health and Metabolism
Fuzhou University (CN)
Openalex Percentile: Top 94%
DNA Repair Mechanisms
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