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      Chemotherapy induced DNA damage response : Convergence of drugs and pathways

      review-article
      1 , 1 , 2 , *
      Cancer Biology & Therapy
      Landes Bioscience
      ATM, ATR, DNA damage, DNA-PK, PIKK, chemotherapy, cisplatin, signaling

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          Abstract

          Chemotherapeutics target rapidly dividing cancer cells by directly or indirectly inducing DNA damage. Upon recognizing DNA damage, cells initiate a variety of signaling pathways collectively referred to as the DNA damage response (DDR). Interestingly, the pathways used to elicit this response are as varied as the types of DNA damage induced. However, the activation of these various pathways has similar results including DNA repair, suppression of global general translation, cell cycle arrest and, ultimately, either cell survival or cell death. This review will focus on a series of chemotherapy-induced DNA lesions and highlight recent advances in our understanding of the DDR, the DNA repair pathways it activates and the cellular consequences of these converging pathways.

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          Most cited references67

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          ATM activation by oxidative stress.

          The ataxia-telangiectasia mutated (ATM) protein kinase is activated by DNA double-strand breaks (DSBs) through the Mre11-Rad50-Nbs1 (MRN) DNA repair complex and orchestrates signaling cascades that initiate the DNA damage response. Cells lacking ATM are also hypersensitive to insults other than DSBs, particularly oxidative stress. We show that oxidation of ATM directly induces ATM activation in the absence of DNA DSBs and the MRN complex. The oxidized form of ATM is a disulfide-cross-linked dimer, and mutation of a critical cysteine residue involved in disulfide bond formation specifically blocked activation through the oxidation pathway. Identification of this pathway explains observations of ATM activation under conditions of oxidative stress and shows that ATM is an important sensor of reactive oxygen species in human cells.
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            ATR-mediated checkpoint pathways regulate phosphorylation and activation of human Chk1.

            Chk1 is an evolutionarily conserved protein kinase that regulates cell cycle progression in response to checkpoint activation. In this study, we demonstrated that agents that block DNA replication or cause certain forms of DNA damage induce the phosphorylation of human Chk1. The phosphorylated form of Chk1 possessed higher intrinsic protein kinase activity and eluted more quickly on gel filtration columns. Serines 317 and 345 were identified as sites of phosphorylation in vivo, and ATR (the ATM- and Rad3-related protein kinase) phosphorylated both of these sites in vitro. Furthermore, phosphorylation of Chk1 on serines 317 and 345 in vivo was ATR dependent. Mutants of Chk1 containing alanine in place of serines 317 and 345 were poorly activated in response to replication blocks or genotoxic stress in vivo, were poorly phosphorylated by ATR in vitro, and were not found in faster-eluting fractions by gel filtration. These findings demonstrate that the activation of Chk1 in response to replication blocks and certain forms of genotoxic stress involves phosphorylation of serines 317 and 345. In addition, this study implicates ATR as a direct upstream activator of Chk1 in human cells.
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              A pathway of double-strand break rejoining dependent upon ATM, Artemis, and proteins locating to gamma-H2AX foci.

              The hereditary disorder ataxia telangiectasia (A-T) is associated with striking cellular radiosensitivity that cannot be attributed to the characterized cell cycle checkpoint defects. By epistasis analysis, we show that ataxia telangiectasia mutated protein (ATM) and Artemis, the protein defective in patients with RS-SCID, function in a common double-strand break (DSB) repair pathway that also requires H2AX, 53BP1, Nbs1, Mre11, and DNA-PK. We show that radiation-induced Artemis hyperphosphorylation is ATM dependent. The DSB repair process requires Artemis nuclease activity and rejoins approximately 10% of radiation-induced DSBs. Our findings are consistent with a model in which ATM is required for Artemis-dependent processing of double-stranded ends with damaged termini. We demonstrate that Artemis is a downstream component of the ATM signaling pathway required uniquely for the DSB repair function but dispensable for ATM-dependent cell cycle checkpoint arrest. The significant radiosensitivity of Artemis-deficient cells demonstrates the importance of this component of DSB repair to survival.
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                Author and article information

                Journal
                Cancer Biol Ther
                Cancer Biol. Ther
                CBT
                Cancer Biology & Therapy
                Landes Bioscience
                1538-4047
                1555-8576
                01 May 2013
                04 February 2013
                04 February 2013
                : 14
                : 5
                : 379-389
                Affiliations
                [1 ]Department of Biochemistry and Molecular Biology; Indiana University School of Medicine; Indianapolis, IN USA
                [2 ]Department of Medicine; Division of Hematology/Oncology; Indiana University School of Medicine; Indianapolis, IN USA
                Author notes
                [* ]Correspondence to: John J. Turchi, Email: jturchi@ 123456iupui.edu
                Article
                2012CBT6112R 23761
                10.4161/cbt.23761
                3672181
                23380594
                2d48eb45-4223-4cfb-b575-39376c150ac2
                Copyright © 2013 Landes Bioscience

                This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.

                History
                : 17 December 2012
                : 23 January 2013
                : 24 January 2013
                Categories
                Review

                Oncology & Radiotherapy
                atm,atr,dna damage,dna-pk,pikk,chemotherapy,cisplatin,signaling
                Oncology & Radiotherapy
                atm, atr, dna damage, dna-pk, pikk, chemotherapy, cisplatin, signaling

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