A mitotic role for the DNA damage-responsive CHK2 kinase

被引:0
|
作者
Ko Sato
Tomohiko Ohta
Ashok R. Venkitaraman
机构
[1] University of Cambridge,Ko Sato and Ashok R. Venkitaraman are in the Department of Oncology and the Medical Research Council Cancer Cell Unit
[2] Hutchison/MRC Research Centre,Tomohiko Ohta is in the Department of Translational Oncology
[3] Hills Road,undefined
[4] Cambridge,undefined
[5] CB2 0XZ arv22@hutchison-mrc.cam.ac.uk,undefined
[6] St Marianna University Graduate School of Medicine,undefined
[7] 2-16-1 Sugao,undefined
[8] Miyamae,undefined
[9] Kawasaki,undefined
[10] 216-8511,undefined
[11] Japan.,undefined
来源
Nature Cell Biology | 2010年 / 12卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
Instability in the structure and number of chromosomes is a trait common to cells from most epithelial cancers. A role in chromosome segregation for a pathway previously implicated in the DNA damage response reveals new connections between the tumour suppressive processes that maintain chromosome integrity.
引用
收藏
页码:424 / 425
页数:1
相关论文
共 50 条
  • [21] A protein phosphatase feedback mechanism regulates the basal phosphorylation of Chk2 kinase in the absence of DNA damage
    Carlessi, Luigi
    Buscemi, Giacomo
    Fontanella, Enrico
    Delia, Domenico
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2010, 1803 (10): : 1213 - 1223
  • [22] Centrosomal Chk2 in DNA damage responses and cell cycle progession
    Golan, Amnon
    Pick, Elah
    Tsvetkov, Lyuben
    Nadler, Yasmine
    Kluger, Harriet
    Stern, David F.
    CELL CYCLE, 2010, 9 (13) : 2647 - 2656
  • [23] Protein phosphatase 2A and CHK2 binding is disrupted by DNA damage
    Freeman, Alyson
    Dapic, Virna
    Monteiro, Alvaro
    CANCER RESEARCH, 2009, 69
  • [24] EDD mediates DNA damage-induced activation of CHK2
    Henderson, Michelle J.
    Munoz, Marcia A.
    Saunders, Darren N.
    Clancy, Jennifer L.
    Russell, Amanda J.
    Williams, Brandi
    Pappin, Darryl
    Khanna, Kum Kum
    Jackson, Stephen P.
    Sutherland, Robert L.
    Watts, Colin K. W.
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (52) : 39990 - 40000
  • [25] DNA damage-activated kinase Chk2 is independent of proliferation or differentiation yet correlates with tissue biology
    Lukas, C
    Bartkova, J
    Latella, L
    Falck, J
    Mailand, N
    Schroeder, T
    Sehested, M
    Lukas, J
    Bartek, J
    CANCER RESEARCH, 2001, 61 (13) : 4990 - 4993
  • [26] Structural and functional versatility of the FHA domain in DNA-damage signaling by the tumor suppressor kinase Chk2
    Li, JJ
    Williams, BL
    Haire, LF
    Goldberg, M
    Walker, E
    Durocher, D
    Yaffe, MB
    Jackson, SP
    Smerdon, SJ
    MOLECULAR CELL, 2002, 9 (05) : 1045 - 1054
  • [27] Chk2 is required for optimal mitotic delay in response to irradiation-induced DNA damage incurred in G2 phase
    Rainey, M. D.
    Black, E. J.
    Zachos, G.
    Gillespie, D. A. F.
    ONCOGENE, 2008, 27 (07) : 896 - 906
  • [28] Chk2 suppresses the oncogenic potential of DNA replication-associated DNA damage
    Stracker, Travis H.
    Couto, Suzana S.
    Cordon-Cardo, Carlos
    Matos, Tulio
    Petrini, John H. J.
    MOLECULAR CELL, 2008, 31 (01) : 21 - 32
  • [29] Suppression of the DNA-damage kinase Chk2 by caffeine leads to functional improvement in endothelial progenitor cells
    Spyridopoulos, L
    Haendeler, J
    CIRCULATION, 2004, 110 (17) : 352 - 352
  • [30] Role of CHK2 in cancer development
    Perona, Rosario
    Moncho-Amor, Veronica
    Machado-Pinilla, Rosario
    Belda-Iniesta, Cristobal
    Sanchez Perez, Isabel
    CLINICAL & TRANSLATIONAL ONCOLOGY, 2008, 10 (09): : 538 - 542