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- W177788487 abstract "There are at least four possible ways in which inhibitors of cyclin-dependent kinases (CDKs) might regulate cell cycle progression (Fig. 1). First, they might determine the duration of G1 phase by setting a threshold above which G1 CDK activity must accumulate before initiation of S-phase. In this threshold role, steady-state levels of CDK inhibitors (CKIs) counteract the temporal accumulation of G1 cyclin/CDK complexes. Second, they might act as checkpoints inducing cell cycle arrest transiently when genomic fidelity is threatened. Chromosome damage or inappropriate segregation of chromosomes may induce cell cycle arrest and initiate DNA repair mechanisms or apoptotic programs. Third, CKIs might allow expedient withdrawal of cells from the cell cycle and a concomitant change in cell fate. In some cases, CKIs might not only regulate the withdrawal from the cell cycle but also affect lineage-specific functions. Fourth, they might function as a gatekeeper of quiescence, keeping the GO cell from inappropriately resuming proliferation. In some cases, tumors arise from well differentiated and non-mitotic cells that inexplicably return to the cell cycle. Over the last 5 years, biochemical, cellular, and molecular analyses of CKIs have combined with genetic analysis of mutant mice deficient in each CKI to address these possible functions. Our current knowledge of the role of CKI in these decisions and speculations about their roles in developmentally regulated cell cycles are discussed below." @default.
- W177788487 created "2016-06-24" @default.
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- W177788487 date "1998-01-01" @default.
- W177788487 modified "2023-09-23" @default.
- W177788487 title "Regulation of the cell cycle by CDK inhibitors" @default.
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- W177788487 doi "https://doi.org/10.1007/978-3-540-69686-5_5" @default.
- W177788487 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/9670321" @default.
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