| Literature DB >> 28616577 |
Ilio Vitale1,2, Gwenola Manic1, Maria Castedo3,4, Guido Kroemer3,4,5,6,7,8,9.
Abstract
Mitotic catastrophe is an oncosuppressive mechanism that targets cells experiencing defective mitoses via the activation of specific cell cycle checkpoints, regulated cell death pathways and/or cell senescence. This prevents the accumulation of karyotypic aberrations, which otherwise may drive oncogenesis and tumor progression. Here, we summarize experimental evidence confirming the role of caspase 2 (CASP2) as the main executor of mitotic catastrophe, and we discuss the signals that activate CASP2 in the presence of mitotic aberrations. In addition, we summarize the main p53-dependent and -independent effector pathways through which CASP2 limits chromosomal instability and non-diploidy, hence mediating robust oncosuppressive functions.Entities:
Keywords: Chromosome instability; mitotic slippage; polyploidy; replication stress; spindle assembly checkpoint; targeted cancer therapy
Year: 2017 PMID: 28616577 PMCID: PMC5462511 DOI: 10.1080/23723556.2017.1299274
Source DB: PubMed Journal: Mol Cell Oncol ISSN: 2372-3556