Literature DB >> 10531013

Caffeine inhibits the checkpoint kinase ATM.

A Blasina1, B D Price, G A Turenne, C H McGowan.   

Abstract

The basis of many anti-cancer therapies is the use of genotoxic agents that damage DNA and thus kill dividing cells. Agents that cause cells to override the DNA-damage checkpoint are predicted to sensitize cells to killing by genotoxic agents. They have therefore been sought as adjuncts in radiation therapy and chemotherapy. One such compound, caffeine, uncouples cell-cycle progression from the replication and repair of DNA [1] [2]. Caffeine therefore servers as a model compound in establishing the principle that agents that override DNA-damage checkpoints can be used to sensitize cells to the killing effects of genotoxic drugs [3]. But despite more than 20 years of use, the molecular mechanisms by which caffeine affects the cell cycle and checkpoint responses have not been identified. We investigated the effects of caffeine on the G2/M DNA-damage checkpoint in human cells. We report that the radiation-induced activation of the kinase Cds1 [4] (also known as Chk2 [5]) is inhibited by caffeine in vivo and that ATM kinase activity is directly inhibited by caffeine in vitro. Inhibition of ATM provides a molecular explanation of the attenuation of DNA-damage checkpoint responses and for the increased radiosensitivity of caffeine-treated cells [6] [7] [8].

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Year:  1999        PMID: 10531013     DOI: 10.1016/s0960-9822(99)80486-2

Source DB:  PubMed          Journal:  Curr Biol        ISSN: 0960-9822            Impact factor:   10.834


  90 in total

1.  Phosphorylation and rapid relocalization of 53BP1 to nuclear foci upon DNA damage.

Authors:  L Anderson; C Henderson; Y Adachi
Journal:  Mol Cell Biol       Date:  2001-03       Impact factor: 4.272

2.  Temporally coordinated assembly and disassembly of replication factories in the absence of DNA synthesis.

Authors:  D S Dimitrova; D M Gilbert
Journal:  Nat Cell Biol       Date:  2000-10       Impact factor: 28.824

Review 3.  Dial 9-1-1 for p53: mechanisms of p53 activation by cellular stress.

Authors:  M Ljungman
Journal:  Neoplasia       Date:  2000 May-Jun       Impact factor: 5.715

4.  An oxidized nucleotide affects DNA replication through activation of protein kinases in Xenopus egg lysates.

Authors:  Toshinori Kai; Rieko Matsunaga; Masami Eguchi; Hiroyuki Kamiya; Hiroshi Kasai; Motoshi Suzuki; Shunji Izuta
Journal:  Nucleic Acids Res       Date:  2002-01-15       Impact factor: 16.971

Review 5.  Control of the G2/M transition.

Authors:  George R Stark; William R Taylor
Journal:  Mol Biotechnol       Date:  2006-03       Impact factor: 2.695

6.  E2F1 induces phosphorylation of p53 that is coincident with p53 accumulation and apoptosis.

Authors:  Harry A Rogoff; Mary T Pickering; Michelle E Debatis; Stephen Jones; Timothy F Kowalik
Journal:  Mol Cell Biol       Date:  2002-08       Impact factor: 4.272

7.  p53 localization at centrosomes during mitosis and postmitotic checkpoint are ATM-dependent and require serine 15 phosphorylation.

Authors:  A Tritarelli; E Oricchio; M Ciciarello; R Mangiacasale; A Palena; P Lavia; S Soddu; E Cundari
Journal:  Mol Biol Cell       Date:  2004-06-04       Impact factor: 4.138

8.  Chemically induced increases and decreases in the rate of expansion of a CAG*CTG triplet repeat.

Authors:  Mário Gomes-Pereira; Darren G Monckton
Journal:  Nucleic Acids Res       Date:  2004-05-20       Impact factor: 16.971

9.  Intra-S-phase checkpoint activation by direct CDK2 inhibition.

Authors:  Yonghong Zhu; Carmen Alvarez; Ronald Doll; Hirokazu Kurata; Xiao Min Schebye; David Parry; Emma Lees
Journal:  Mol Cell Biol       Date:  2004-07       Impact factor: 4.272

10.  Environmental exposure, chlorinated drinking water, and bladder cancer.

Authors:  Peter J Goebell; Cristina M Villanueva; Albert W Rettenmeier; Herbert Rübben; Manolis Kogevinas
Journal:  World J Urol       Date:  2003-12-20       Impact factor: 4.226

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