Literature DB >> 2055943

Cellular senescence: a reflection of normal growth control, differentiation, or aging?

M Peacocke1, J Campisi.   

Abstract

Normal cells, with few exceptions, cannot proliferate indefinitely. Cell populations--in vivo and in culture--generally undergo only a limited number of doublings before proliferation invariably and irreversibly ceases. This process has been termed the finite lifespan phenotype or cellular senescence. There is long-standing, albeit indirect, evidence that cellular senescence plays an important role in complex biological processes as diverse as normal growth control, differentiation, development, aging, and tumorigenesis. In recent years, it has been possible to develop a molecular framework for understanding some of the fundamental features of cellular senescence. This framework derives primarily from the physiology, genetics, and molecular biology of cells undergoing senescence in culture. Our understanding of senescence, and the mechanisms that control it, is still in its infancy. Nonetheless, recent data raise some intriguing possibilities regarding potential molecular bases for the links between senescence in culture and normal and abnormal growth control, differentiation, and aging.

Mesh:

Substances:

Year:  1991        PMID: 2055943     DOI: 10.1002/jcb.240450205

Source DB:  PubMed          Journal:  J Cell Biochem        ISSN: 0730-2312            Impact factor:   4.429


  7 in total

Review 1.  Pathways of oncogene-induced senescence in human melanocytic cells.

Authors:  Rajat Bansal; Mikhail A Nikiforov
Journal:  Cell Cycle       Date:  2010-07-03       Impact factor: 4.534

2.  Human fibroblast commitment to a senescence-like state in response to histone deacetylase inhibitors is cell cycle dependent.

Authors:  V V Ogryzko; T H Hirai; V R Russanova; D A Barbie; B H Howard
Journal:  Mol Cell Biol       Date:  1996-09       Impact factor: 4.272

3.  Senescence-like growth arrest induced by hydrogen peroxide in human diploid fibroblast F65 cells.

Authors:  Q Chen; B N Ames
Journal:  Proc Natl Acad Sci U S A       Date:  1994-05-10       Impact factor: 11.205

4.  Oxidative DNA damage and senescence of human diploid fibroblast cells.

Authors:  Q Chen; A Fischer; J D Reagan; L J Yan; B N Ames
Journal:  Proc Natl Acad Sci U S A       Date:  1995-05-09       Impact factor: 11.205

5.  Potentiated bradykinin-induced increase of 1,2-diacylglycerol generation and phospholipase D activity in human senescent fibroblasts.

Authors:  E Meacci; V Vasta; P Faraoni; M Farnararo; P Bruni
Journal:  Biochem J       Date:  1995-12-15       Impact factor: 3.857

6.  Characterisation of Plasmodium falciparum populations selected on the human endothelial receptors P-selectin, E-selectin, CD9 and CD151.

Authors:  Nahla Galal Metwally; Ann-Kathrin Tilly; Pedro Lubiana; Lisa K Roth; Michael Dörpinghaus; Stephan Lorenzen; Kathrin Schuldt; Susanne Witt; Anna Bachmann; Henning Tidow; Thomas Gutsmann; Thorsten Burmester; Thomas Roeder; Egbert Tannich; Iris Bruchhaus
Journal:  Sci Rep       Date:  2017-06-22       Impact factor: 4.379

Review 7.  Diverse Roles of Ceramide in the Progression and Pathogenesis of Alzheimer's Disease.

Authors:  Md Riad Chowdhury; Hee Kyung Jin; Jae-Sung Bae
Journal:  Biomedicines       Date:  2022-08-12
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.