Nucleus tumor suppressors

In apoptotic cell death, several factors such as growth factors, NO, the tumor suppressor gene p53, and the protein encoded by this gene contribute to the process that leads to cell death. One of the functions of p53 protein is the activation of apoptosis if a cell is transformed to a malignant cell. Apoptosis typically leads to the formation of smaller membrane-encapsulated particles within the cell. Apoptotic cell death begins in the nucleus and proceeds to other parts of the cell. The death process may be quite advanced before it can... 

New examples of cellular rhythms have recently been uncovered (Table II). These include periodic changes in the intracellular concentration of the transcription factor NF-KB and of the tumor suppressors p53, stress-induced oscillations in the transport of the transcription factor Msn2 between cytoplasm and nucleus in yeast, the segmentation clock that is responsible for the... 

Caspase-8 activates the effector caspases either directly, or indirectly by promoting the cytochrome c (see p. 140) from mitochondria. Once in the cytoplasm, cytochrome c binds to and activates the protein Apaf-1 (not shown) and thus triggers the caspase cascade. Apoptotic signals can also come from the cell nucleus. If irreparable DNA damage is present, the p53 protein (see p. 394)—the product of a tumor suppressor gene—promotes apoptosis and thus helps eliminate the defective cell. 

Tordk, I. Strand, D., Schmitt, R., Tick, G., Torok, T., Kiss, I., and Mechler, B. M. (1995), The overgrown hematopoietic organs-31 tumor suppressor gene of Drosophila encodes an importin-like protein accumulating in the nucleus at the onset of mitosis, J. Cell. BioL 129, 1473-1489. 

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