Literature DB >> 14702100

When cells get stressed: an integrative view of cellular senescence.

Ittai Ben-Porath1, Robert A Weinberg.   

Abstract

Cells entering a state of senescence undergo a permanent cell cycle arrest, accompanied by a set of functional and morphological changes. Senescence of cells occurs following an extended period of proliferation in culture or in response to various physiologic stresses, yet little is known about the role this phenomenon plays in vivo. The study of senescence has focused largely on its hypothesized role as a barrier to extended cell division, governed by a division-counting mechanism in the form of telomere length. Here, we discuss the biological functions of cellular senescence and suggest that it should be viewed in terms of its role as a general cellular stress response program, rather than strictly as a barrier to unlimited cycles of cell growth and division. We also discuss the relative roles played by telomere shortening and telomere uncapping in the induction of senescence.

Mesh:

Year:  2004        PMID: 14702100      PMCID: PMC300889          DOI: 10.1172/JCI20663

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  56 in total

1.  Senescence induced by altered telomere state, not telomere loss.

Authors:  Jan Karlseder; Agata Smogorzewska; Titia de Lange
Journal:  Science       Date:  2002-03-29       Impact factor: 47.728

2.  Limits to lifespan.

Authors:  Alison C Lloyd
Journal:  Nat Cell Biol       Date:  2002-02       Impact factor: 28.824

Review 3.  Historical claims and current interpretations of replicative aging.

Authors:  Woodring E Wright; Jerry W Shay
Journal:  Nat Biotechnol       Date:  2002-07       Impact factor: 54.908

4.  Expression of human telomerase (hTERT) does not prevent stress-induced senescence in normal human fibroblasts but protects the cells from stress-induced apoptosis and necrosis.

Authors:  Vera Gorbunova; Andrei Seluanov; Olivia M Pereira-Smith
Journal:  J Biol Chem       Date:  2002-07-24       Impact factor: 5.157

5.  p16(INK4a) inactivation is not required to immortalize human mammary epithelial cells.

Authors:  Brittney-Shea Herbert; Woodring E Wright; Jerry W Shay
Journal:  Oncogene       Date:  2002-11-07       Impact factor: 9.867

6.  Loss of p16Ink4a with retention of p19Arf predisposes mice to tumorigenesis.

Authors:  N E Sharpless; N Bardeesy; K H Lee; D Carrasco; D H Castrillon; A J Aguirre; E A Wu; J W Horner; R A DePinho
Journal:  Nature       Date:  2001-09-06       Impact factor: 49.962

7.  Loss of p16Ink4a confers susceptibility to metastatic melanoma in mice.

Authors:  P Krimpenfort; K C Quon; W J Mooi; A Loonstra; A Berns
Journal:  Nature       Date:  2001-09-06       Impact factor: 49.962

8.  A senescence program controlled by p53 and p16INK4a contributes to the outcome of cancer therapy.

Authors:  Clemens A Schmitt; Jordan S Fridman; Meng Yang; Soyoung Lee; Eugene Baranov; Robert M Hoffman; Scott W Lowe
Journal:  Cell       Date:  2002-05-03       Impact factor: 41.582

9.  Different telomere damage signaling pathways in human and mouse cells.

Authors:  Agata Smogorzewska; Titia de Lange
Journal:  EMBO J       Date:  2002-08-15       Impact factor: 11.598

Review 10.  The disparity between human cell senescence in vitro and lifelong replication in vivo.

Authors:  Harry Rubin
Journal:  Nat Biotechnol       Date:  2002-07       Impact factor: 54.908

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  118 in total

1.  Enhancement of intervertebral disc cell senescence by WNT/β-catenin signaling-induced matrix metalloproteinase expression.

Authors:  Akihiko Hiyama; Daisuke Sakai; Makarand V Risbud; Masahiro Tanaka; Fumiyuki Arai; Koichiro Abe; Joji Mochida
Journal:  Arthritis Rheum       Date:  2010-10

Review 2.  Do tumor-suppressive mechanisms contribute to organism aging by inducing stem cell senescence?

Authors:  Pier Giuseppe Pelicci
Journal:  J Clin Invest       Date:  2004-01       Impact factor: 14.808

3.  Presence of somatic mutations in most early-stage pancreatic intraepithelial neoplasia.

Authors:  Mitsuro Kanda; Hanno Matthaei; Jian Wu; Seung-Mo Hong; Jun Yu; Michael Borges; Ralph H Hruban; Anirban Maitra; Kenneth Kinzler; Bert Vogelstein; Michael Goggins
Journal:  Gastroenterology       Date:  2012-01-05       Impact factor: 22.682

Review 4.  Epigenetic control of aging.

Authors:  Ursula Muñoz-Najar; John M Sedivy
Journal:  Antioxid Redox Signal       Date:  2010-11-22       Impact factor: 8.401

5.  Oncogenic KRas suppresses inflammation-associated senescence of pancreatic ductal cells.

Authors:  Kyoung Eun Lee; Dafna Bar-Sagi
Journal:  Cancer Cell       Date:  2010-11-16       Impact factor: 31.743

Review 6.  Assessing cell and organ senescence biomarkers.

Authors:  Bruno Bernardes de Jesus; Maria A Blasco
Journal:  Circ Res       Date:  2012-06-22       Impact factor: 17.367

7.  Longitudinal analysis of short-term high-fat diet on endothelial senescence in baboons.

Authors:  Qiang Shi; Peter J Hornsby; Qinghe Meng; Jane F Vandeberg; John L Vandeberg
Journal:  Am J Cardiovasc Dis       Date:  2013-08-16

8.  Co-regulation of p16INK4A and migratory genes in culture conditions that lead to premature senescence in human keratinocytes.

Authors:  Benjamin W Darbro; Galen B Schneider; Aloysius J Klingelhutz
Journal:  J Invest Dermatol       Date:  2005-09       Impact factor: 8.551

Review 9.  The type 2 inositol 1,4,5-trisphosphate receptor, emerging functions for an intriguing Ca²⁺-release channel.

Authors:  Tamara Vervloessem; David I Yule; Geert Bultynck; Jan B Parys
Journal:  Biochim Biophys Acta       Date:  2014-12-10

10.  Age-dependent impaired neurogenic differentiation capacity of dental stem cell is associated with Wnt/β-catenin signaling.

Authors:  Xingmei Feng; Jing Xing; Guijuan Feng; Aimin Sang; Biyu Shen; Yue Xu; Jinxia Jiang; Suzhe Liu; Wei Tan; Zhifeng Gu; Liren Li
Journal:  Cell Mol Neurobiol       Date:  2013-09-17       Impact factor: 5.046

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