The overlapping, yet independent, functions of ATM, ATR and p53 in coordinating cell cycle transitio

来源 :The 16th Ataxia-Telangiectasia Workshop (ATW-2015)6th Intern | 被引量 : 0次 | 上传用户:pengtao2222
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  Activation of the DNA-damage response (DDR) can enable cancer cells to resist the lethal effects of genotoxic cancer therapy.However, cancer cells frequently exhibit defects in components of the DNA-damage response (DDR) and may consequently become highly dependent on remaining DDR pathways to survive DNA damage.Targeting such remaining DDR pathways has become a valuable new strategy for personalised cancer therapy, and an attractive target for this approach is the apical DDR kinase Ataxia-telangiectasia and Rad3-related (ATR).
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