The Activation of DNA Damage Response is the Basis of the Occurrence, Development and Resistance to Radioor Chemotherapy in Ovarian Cancer |Biomedgrid
Journal: American Journal of Biomedical Science & Research (Vol.11, No. 3)Publication Date: 2020-12-15
Authors : Changsheng Peng; Wei Zhang;
Page : 199-200
Keywords : Genome; Harsh environment; Genotoxicity; Chemotherapy; Radiotherapy;
Abstract
Genome surveillance system is critical for eukaryotic cells to maintain genome stability [1,2]. Cell cycle checkpoints is quickly activated upon detecting various forms of DNA lesions, ensued by loading of repair factors to eliminate DNA damage [3]. ATM (Ataxia-Telangiectasia mutated) and ATR (ATM and Rad 3-related), the upstream checkpoint kinase, initiate damage detection and signal transduction after exposure to genotoxic insults including ionizing radiation or chemotherapeutic reagents [4]. To eliminate DNA lesions generated during genomic replication, ATR-dependent replication stress is activated to modulates the activities of the cell cycle regulator to halt cell cycle.
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