Ampolini Elizabeth A, Jimenez-Sainz Judit, Long David T
Department of Biochemistry and Molecular Biology, Hollings Cancer Center, Medical University of South Carolina, Charleston, SC, 29425, USA.
Target Oncol. 2025 Mar;20(2):281-297. doi: 10.1007/s11523-025-01136-6. Epub 2025 Mar 1.
The ataxia-telangiectasia mutated (ATM) protein kinase plays a critical role in activating the cellular response to DNA double-strand breaks and promoting homology-directed repair. ATM is frequently mutated in cancer, contributing to an accumulation of DNA damage that drives genomic instability. To exploit cancer cells' inherent vulnerability to DNA damage, various small molecule inhibitors have been developed that target ATM. ATM inhibitors have shown great versatility in preclinical studies and increasing use in the clinic. Here, we review the development of ATM inhibitors and their role in cancer therapy. We describe their limitations and the advances that have led to increases in both the number and diversity of active clinical trials targeting ATM. We also discuss ATM's role in personalized medicine and the current challenges to more widespread use of ATM inhibitors in the clinic.
共济失调毛细血管扩张症突变(ATM)蛋白激酶在激活细胞对DNA双链断裂的反应以及促进同源定向修复中起关键作用。ATM在癌症中经常发生突变,导致DNA损伤积累,进而引发基因组不稳定。为了利用癌细胞对DNA损伤的固有脆弱性,已开发出多种靶向ATM的小分子抑制剂。ATM抑制剂在临床前研究中显示出巨大的通用性,并且在临床上的应用越来越多。在这里,我们综述了ATM抑制剂的发展及其在癌症治疗中的作用。我们描述了它们的局限性以及导致针对ATM的活性临床试验数量和多样性增加的进展。我们还讨论了ATM在个性化医疗中的作用以及目前在临床上更广泛使用ATM抑制剂所面临的挑战。