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Review:DNA-damage response network at the crossroads of cell-cycle checkpoints, cellular senescence and apoptosis
作者姓名:SCHMITT Estelle  PAQUET Claudie  BEAUCHEMIN Myriam  BERTRAND Richard
作者单位:Notre Dame Hospital and Montreal Cancer Institute Research Centre of University of Montreal Hospital Centre (CRCHUM) Montreal (Que) H2L 4M1 Canada,Notre Dame Hospital and Montreal Cancer Institute Research Centre of University of Montreal Hospital Centre (CRCHUM) Montreal (Que) H2L 4M1 Canada,Notre Dame Hospital and Montreal Cancer Institute Research Centre of University of Montreal Hospital Centre (CRCHUM) Montreal (Que) H2L 4M1 Canada,Notre Dame Hospital and Montreal Cancer Institute Research Centre of University of Montreal Hospital Centre (CRCHUM) Montreal (Que) H2L 4M1 Canada Medicine Department University of Montreal Montreal (Que) H3C 3J7 Canada
基金项目:the Canadian Institutes of Health Research and the Cancer Research Society, and fellowships by the Health Research Funds of Quebec, Canada
摘    要:Tissue homeostasis requires a carefully-orchestrated balance between cell proliferation, cellular senescence and cell death. Cells proliferate through a cell cycle that is tightly regulated by cyclin-dependent kinase activities. Cellular senescence is a safeguard program limiting the proliferative competence of cells in living organisms. Apoptosis eliminates unwanted cells by the coordinated activity of gene products that regulate and effect cell death. The intimate link between the cell cycle, cellular senes- cence, apoptosis regulation, cancer development and tumor responses to cancer treatment has become eminently apparent. Extensive research on tumor suppressor genes, oncogenes, the cell cycle and apoptosis regulatory genes has revealed how the DNA damage-sensing and -signaling pathways, referred to as the DNA-damage response network, are tied to cell proliferation, cell-cycle arrest, cellular senescence and apoptosis. DNA-damage responses are complex, involving “sensor” proteins that sense the damage, and transmit signals to “transducer” proteins, which, in turn, convey the signals to numerous “effector” proteins implicated in specific cellular pathways, including DNA repair mechanisms, cell-cycle checkpoints, cellular senescence and apoptosis. The Bcl-2 family of proteins stands among the most crucial regulators of apoptosis and performs vital functions in deciding whether a cell will live or die after cancer chemotherapy and irradiation. In addition, several studies have now revealed that members of the Bcl-2 family also interface with the cell cycle, DNA repair/recombination and cellular senescence, effects that are generally distinct from their function in apoptosis. In this review, we report progress in understanding the molecular networks that regulate cell-cycle checkpoints, cellular senescence and apoptosis after DNA damage, and discuss the influence of some Bcl-2 family members on cell-cycle checkpoint regulation.


Review:DNA-damage response network at the crossroads of cell-cycle checkpoints, cellular senescence and apoptosis
SCHMITT Estelle,PAQUET Claudie,BEAUCHEMIN Myriam,BERTRAND Richard.Review:DNA-damage response network at the crossroads of cell-cycle checkpoints, cellular senescence and apoptosis[J].Journal of Zhejiang University Science,2007(6).
Authors:SCHMITT Estelle  PAQUET Claudie  BEAUCHEMIN Myriam  BERTRAND Richard
Institution:SCHMITT Estelle1,PAQUET Claudie1,BEAUCHEMIN Myriam1,BERTRAND Richard1,2
Abstract:
Keywords:DNA-damage response network  Cell cycle  Cellular senescence  Apoptosis  Bcl-2 family
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