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 |
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creator | Smith, James R. 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. |
doi_str_mv | 10.1126/science.273.5271.63 |
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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.</description><identifier>ISSN: 0036-8075</identifier><identifier>EISSN: 1095-9203</identifier><identifier>DOI: 10.1126/science.273.5271.63</identifier><identifier>PMID: 8658197</identifier><identifier>CODEN: SCIEAS</identifier><language>eng</language><publisher>United States: American Society for the Advancement of Science</publisher><subject>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</subject><ispartof>Science (American Association for the Advancement of Science), 1996-07, Vol.273 (5271), p.63-67</ispartof><rights>Copyright 1996 American Association for the Advancement of Science</rights><rights>COPYRIGHT 1996 American Association for the Advancement of Science</rights><rights>Copyright American Association for the Advancement of Science Jul 5, 1996</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c746t-e825e77c2f7e5b84ada88e050fab534a4d2a4627cf5d283baea545ca2f57be5d3</citedby><cites>FETCH-LOGICAL-c746t-e825e77c2f7e5b84ada88e050fab534a4d2a4627cf5d283baea545ca2f57be5d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/2890039$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/2890039$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,803,2884,2885,27924,27925,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8658197$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Smith, James R.</creatorcontrib><creatorcontrib>Pereira-Smith, Olivia M.</creatorcontrib><title>Replicative Senescence: Implications for in Vivo Aging and Tumor Suppression</title><title>Science (American Association for the Advancement of Science)</title><addtitle>Science</addtitle><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.</description><subject>Aging</subject><subject>Aging (Biology)</subject><subject>Aging - genetics</subject><subject>Animals</subject><subject>Cell culture techniques</subject><subject>Cell cycle</subject><subject>Cell Division - genetics</subject><subject>Cell growth</subject><subject>Cell lines</subject><subject>Cellular biology</subject><subject>Cellular senescence</subject><subject>Cellular Senescence - genetics</subject><subject>Epithelial cells</subject><subject>Fibroblasts</subject><subject>Gene Expression</subject><subject>Genes</subject><subject>Genes, Tumor Suppressor</subject><subject>Genetic aspects</subject><subject>Genetic Disorders</subject><subject>Genetics</subject><subject>Horizons in Aging</subject><subject>Humans</subject><subject>Individualized Instruction</subject><subject>Molecular biology</subject><subject>Neoplasms - etiology</subject><subject>Neoplasms - genetics</subject><subject>Somatic cells</subject><subject>T lymphocytes</subject><subject>Telomerase - metabolism</subject><subject>Telomere - metabolism</subject><subject>Tumor suppressor genes</subject><subject>Tumors</subject><subject>Tumour suppressor 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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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