Replicative Senescence: Implications for in Vivo Aging and Tumor Suppression

Normal cells have limited proliferative potential in culture, a fact that has been the basis of their use as a model for replicative senescence for many years. Recent molecular analyses have identified numerous changes in gene expression that occur as cells become senescent, and the results indicate...

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Veröffentlicht in:Science (American Association for the Advancement of Science) 1996-07, Vol.273 (5271), p.63-67
Hauptverfasser: Smith, James R., Pereira-Smith, Olivia M.
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Pereira-Smith, Olivia M.
description Normal cells have limited proliferative potential in culture, a fact that has been the basis of their use as a model for replicative senescence for many years. Recent molecular analyses have identified numerous changes in gene expression that occur as cells become senescent, and the results indicate that multiple levels of control contribute to the irreversible growth arrest. These include repression of growth stimulatory genes, overexpression of growth inhibitory genes, and interference with downstream pathways. Studies with cell types other than fibroblasts will better define the role of cell senescence in the aging process and in tumorigenesis.
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subjects Aging
Aging (Biology)
Aging - genetics
Animals
Cell culture techniques
Cell cycle
Cell Division - genetics
Cell growth
Cell lines
Cellular biology
Cellular senescence
Cellular Senescence - genetics
Epithelial cells
Fibroblasts
Gene Expression
Genes
Genes, Tumor Suppressor
Genetic aspects
Genetic Disorders
Genetics
Horizons in Aging
Humans
Individualized Instruction
Molecular biology
Neoplasms - etiology
Neoplasms - genetics
Somatic cells
T lymphocytes
Telomerase - metabolism
Telomere - metabolism
Tumor suppressor genes
Tumors
Tumour suppressor genes
title Replicative Senescence: Implications for in Vivo Aging and Tumor Suppression
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