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Targeting the ATM pathway in cancer: Opportunities, challenges and personalized therapeutic strategies
1Department of Biological Sciences, Research Center of Ecomimetics, Chonnam National University, Gwangju 61186, Republic of Korea.
Abstract:
Ataxia telangiectasia mutated (ATM) kinase plays a pivotal role in orchestrating the DNA damage response, maintaining genomic stability, and regulating various cellular processes. This review provides a comprehensive analysis of ATM's structure, activation mechanisms, and various functions in cancer development, progression, and treatment. I discuss ATM's dual nature as both a tumor suppressor and potential promoter of cancer cell survival in certain contexts. The article explores the complex signaling pathways mediated by ATM, its interactions with other DNA repair mechanisms, and its influence on cell cycle checkpoints, apoptosis, and metabolism. I examine the clinical implications of ATM alterations, including their impact on cancer predisposition, prognosis, and treatment response. The review highlights recent advances in ATM-targeted therapies, discussing ongoing clinical trials of ATM inhibitors and their potential in combination with other treatment modalities. I also address the challenges in developing effective biomarkers for ATM activity and patient selection strategies for personalized cancer therapy. Finally, I outline future research directions, emphasizing the need for refined biomarker development, optimized combination therapies, and strategies to overcome potential resistance mechanisms. This comprehensive overview underscores the critical importance of ATM in cancer biology and its emerging potential as a therapeutic target in precision oncology.
Insights
Ataxia telangiectasia mutated (ATM) kinase is crucial for DNA repair and genomic stability. This review explores ATM
Area of Science:
- Molecular Biology
- Genetics
- Oncology
Background:
- Ataxia telangiectasia mutated (ATM) kinase is a key regulator of the DNA damage response (DDR).
- ATM's role in maintaining genomic stability is critical for preventing cancer development.
- Dysregulation of ATM signaling is implicated in various human cancers.
Purpose of the Study:
- To provide a comprehensive review of ATM's structure, activation, and functions in cancer.
- To discuss the dual role of ATM in cancer suppression and promotion.
- To examine the clinical implications of ATM alterations and ATM-targeted therapies.
Main Methods:
- Literature review of ATM's role in DNA damage response, cell cycle regulation, apoptosis, and metabolism.
- Analysis of ATM's interactions with other DNA repair pathways.
- Examination of clinical data on ATM alterations and therapeutic strategies.
Main Results:
- ATM exhibits context-dependent roles as both a tumor suppressor and a promoter of cancer cell survival.
- ATM signaling pathways are complex and interact with multiple cellular processes.
- ATM alterations impact cancer predisposition, prognosis, and treatment response.
Conclusions:
- ATM is a critical factor in cancer biology with significant therapeutic potential.
- Targeting ATM offers promising avenues for precision oncology, but challenges remain.
- Further research is needed for refined biomarkers, optimized combination therapies, and overcoming resistance.
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