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ID 63232
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Author
Ueno, Sayaka Department of Clinical Genomic Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Sudo, Tamotsu Section of Translational Research, Hyogo Cancer Center
Hirasawa, Akira Department of Clinical Genomic Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University Kaken ID researchmap
Abstract
Ataxia-telangiectasia mutated (ATM) functions as a key initiator and coordinator of DNA damage and cellular stress responses. ATM signaling pathways contain many downstream targets that regulate multiple important cellular processes, including DNA damage repair, apoptosis, cell cycle arrest, oxidative sensing, and proliferation. Over the past few decades, associations between germline ATM pathogenic variants and cancer risk have been reported, particularly for breast and pancreatic cancers. In addition, given that ATM plays a critical role in repairing double-strand breaks, inhibiting other DNA repair pathways could be a synthetic lethal approach. Based on this rationale, several DNA damage response inhibitors are currently being tested in ATM-deficient cancers. In this review, we discuss the current knowledge related to the structure of the ATM gene, function of ATM kinase, clinical significance of ATM germline pathogenic variants in patients with hereditary cancers, and ongoing efforts to target ATM for the benefit of cancer patients.
Keywords
hereditary tumors
ATM
DNA damage
redox homeostasis
tumor profiling
precision therapy
Published Date
2022-01-04
Publication Title
International Journal Of Molecular Sciences
Volume
volume23
Issue
issue1
Publisher
MDPI
Start Page
523
ISSN
1422-0067
NCID
AA12038549
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© 2022 by the authors.
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Related Url
isVersionOf https://doi.org/10.3390/ijms23010523
License
https://creativecommons.org/licenses/by/4.0/