Abstract：
:Chemoresistance, radioresistance, and the challenge of achieving complete resection are major driving forces in the search for more robust and targeted anticancer therapies. Targeting the DNA damage response has recently attracted research interest, as these processes are enhanced in tumour cells. The major replication stress responder is ATM and Rad3-related (ATR) kinase, which is attracting attention worldwide with four drug candidates currently in phase I/II clinical trials. This review addresses a potent and selective small-molecule ATR inhibitor, which is known as VX-970 (also known as berzosertib or M6620), and summarizes the existing preclinical data to provide deep insight regarding its real potential. We also outline the transition from preclinical to clinical studies, as well as its relationships with other clinical candidates (AZD6738, VX-803 [M4344], and BAY1895344). The results suggest that VX-970 is indeed a promising anticancer drug that can be used both as monotherapy and in combination with either chemotherapy or radiotherapy strategies. Based on patient anamnesis and biomarker identification, VX-970 could become a valuable tool for oncologists in the fight against cancer.
journal_name
Pharmacol Therjournal_title
Pharmacology & therapeuticsauthors
Gorecki L,Andrs M,Rezacova M,Korabecny Jdoi
10.1016/j.pharmthera.2020.107518subject
Has Abstractpub_date
2020-06-01 00:00:00pages
107518eissn
0163-7258issn
1879-016Xpii
S0163-7258(20)30046-2journal_volume
210pub_type
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journal_title：Pharmacology & therapeutics
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