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Review
. 2003 Jun;36(3):165-75.
doi: 10.1046/j.1365-2184.2003.00267.x.

Cell cycle and apoptosis

Affiliations
Review

Cell cycle and apoptosis

Katrien Vermeulen et al. Cell Prolif. 2003 Jun.

Abstract

Apoptosis and proliferation are intimately coupled. Some cell cycle regulators can influence both cell division and programmed cell death. The linkage of cell cycle and apoptosis has been recognized for c-Myc, p53, pRb, Ras, PKA, PKC, Bcl-2, NF-kappa B, CDK, cyclins and CKI. This review summarizes the different functions of the proteins presently known to control both apoptosis and cell cycle progression. These proteins can influence apoptosis or proliferation but different variables, including cell type, cellular environment and genetic background, make it difficult to predict the outcome of cell proliferation, cell cycle arrest or cell death. These important decisions of cell proliferation or cell death are likely to be controlled by more than one signal and are necessary to ensure a proper cellular response.

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Figures

Figure 1
Figure 1
The role of c‐Myc in cell cycle and apoptosis.
Figure 2
Figure 2
The role of Ras in cell cycle and apoptosis.

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References

    1. Adams JM, Cory S (1998) The Bcl‐2 protein family: arbiters of cell survival. Science 281, 1322. - PubMed
    1. Adjei AA (2001) Blocking oncogenic Ras signaling for cancer therapy. J. Natl Cancer Inst 93, 1062. - PubMed
    1. Agarwal ML, Taylor WR, Chernov MV, Chernova OB, Stark GR (1998) The p53 network. J. Biol. Chem. 273, 1. - PubMed
    1. De Alboran IM, O'Hagan RC, Gartner F, Malynn B, Davidson L, Rickert R., Rajewsky K, Depinho RA, Alt FW (2001) Analysis of C‐MYC function in normal cells via conditional gene‐targeted mutation. Immunity. 14, 45. - PubMed
    1. Alvarez. E, Northwood IC, Gonzalez. FA, Latour DA, Seth A, Abate C, Curran T, Davis RJ (1991) Pro‐Leu‐Ser/Thr‐Pro is a consensus primary sequence for substrate protein phosphorylation. Characterization of the phosphorylation of c‐myc and c‐jun proteins by an epidermal growth factor receptor threonine 669 protein kinase. J. Biol. Chem. 266, 15277. - PubMed