Literature DB >> 12543256

Cellular senescence and apoptosis: how cellular responses might influence aging phenotypes.

Judith Campisi1.   

Abstract

Aging in complex multi-cellular organisms such as mammals entails distinctive changes in cells and molecules that ultimately compromise the fitness of adult organisms. These cellular and molecular changes lead to the phenotypes we recognize as aging. This review discusses some of the cellular and molecular changes that occur with age, specifically changes that occur as a result of cellular responses that evolved to ameliorate the inevitable damage that is caused by endogenous and environmental insults. Because the force of natural selection declines with age, it is likely that these processes were never optimized during their evolution to benefit old organisms. That is, some age-related changes may be the result of gene activities that were selected for their beneficial effects in young organisms, but the same gene activities may have unselected, deleterious effects in old organisms, a phenomenon termed antagonistic pleiotropy. Two cellular processes, apoptosis and cellular senescence, may be examples of antagonistic pleiotropy. Both processes are essential for the viability and fitness of young organisms, but may contribute to aging phenotypes, including certain age-related diseases.

Mesh:

Year:  2003        PMID: 12543256     DOI: 10.1016/s0531-5565(02)00152-3

Source DB:  PubMed          Journal:  Exp Gerontol        ISSN: 0531-5565            Impact factor:   4.032


  55 in total

Review 1.  The immune system in the elderly: activation-induced and damage-induced apoptosis.

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Journal:  Immunol Res       Date:  2004       Impact factor: 2.829

2.  Differential patterns of apoptosis in response to aging in Drosophila.

Authors:  Jie Zheng; Scott W Edelman; Grace Tharmarajah; David W Walker; Scott D Pletcher; Laurent Seroude
Journal:  Proc Natl Acad Sci U S A       Date:  2005-08-12       Impact factor: 11.205

3.  The biology of aging and frailty.

Authors:  Neal S Fedarko
Journal:  Clin Geriatr Med       Date:  2011-02       Impact factor: 3.076

4.  Regeneration of kidney tissue using in vitro cultured fetal kidney cells.

Authors:  Sang Soo Kim; So Jung Gwak; Joungho Han; Moon Hyang Park; Kang Won Song; Byung Soo Kim
Journal:  Exp Mol Med       Date:  2008-08-31       Impact factor: 8.718

5.  Age-dependent changes in cell proliferation and cell death in the periodontal tissue and the submandibular gland in mice: a comparison with other tissues and organs.

Authors:  Norio Enoki; Tamotsu Kiyoshima; Takako Sakai; Ieyoshi Kobayashi; Keiko Takahashi; Yoshihiro Terada; Hidetaka Sakai
Journal:  J Mol Histol       Date:  2007-06-20       Impact factor: 2.611

Review 6.  Life history trade-offs in cancer evolution.

Authors:  C Athena Aktipis; Amy M Boddy; Robert A Gatenby; Joel S Brown; Carlo C Maley
Journal:  Nat Rev Cancer       Date:  2013-11-11       Impact factor: 60.716

Review 7.  TGF-β1 Signaling and Tissue Fibrosis.

Authors:  Kevin K Kim; Dean Sheppard; Harold A Chapman
Journal:  Cold Spring Harb Perspect Biol       Date:  2018-04-02       Impact factor: 10.005

Review 8.  The impact of cerebrovascular aging on vascular cognitive impairment and dementia.

Authors:  Tuo Yang; Yang Sun; Zhengyu Lu; Rehana K Leak; Feng Zhang
Journal:  Ageing Res Rev       Date:  2016-09-28       Impact factor: 10.895

Review 9.  Aging genomes: a necessary evil in the logic of life.

Authors:  Jan Vijg
Journal:  Bioessays       Date:  2014-01-25       Impact factor: 4.345

10.  Role of SV40 integration site at chromosomal interval 1q21.1 in immortalized CRL2504 cells.

Authors:  Jinglan Liu; Gurpreet Kaur; Vikramjit K Zhawar; Drazen B Zimonjic; Nicholas C Popescu; Raj P Kandpal; Raghbir S Athwal
Journal:  Cancer Res       Date:  2009-09-29       Impact factor: 12.701

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