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PMID: 18171426 Published · ppublish English Journal Article Review

FOXO transcription factors in ageing and cancer.

Acta physiologica (Oxford, England) ·Vol. 192 ·No. 1 ·2008-01-00 ·Pages 19-28

Greer EL, Brunet A

Abstract

Ageing is associated with an increased onset of cancer. Understanding the molecular mechanisms that underlie the age dependency of cancer will have important implications for preventing and treating this pathology. The signalling pathway connecting insulin and FOXO transcription factors provides the most compelling example for a conserved genetic pathway at the interface between ageing and cancer. FOXO transcription factors (FOXO) promote longevity and tumour suppression. FOXO transcription factors are directly phosphorylated in response to insulin/growth factor signalling by the protein kinase Akt, thereby causing their sequestration in the cytoplasm. In the absence of insulin/growth factors, FOXO factors translocate to the nucleus where they trigger a range of cellular responses, including resistance to oxidative stress, a phenotype highly coupled with lifespan extension. FOXO factors integrate stress stimuli via phosphorylation, acetylation and mono-ubiquitination of a series of regulatory sites. Understanding how FOXO proteins integrate environmental conditions to control specific gene expression programmes will be pivotal in identifying ways to slow the onset of cancer in ageing individuals.

MeSH Terms
Aging/physiology Animals Cell Cycle Proteins/physiology Forkhead Transcription Factors/physiology Humans Longevity Mice Neoplasms/physiopathology Phosphorylation Signal Transduction/physiology
Chemicals
Cell Cycle Proteins Forkhead Transcription Factors
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Greer E L
Department of Genetics, Stanford University, Stanford, CA 94305, USA. [email protected]
Brunet A
Article Info
Journal
Acta physiologica (Oxford, England)
Abbr.
Acta Physiol (Oxf)
ISSN
1748-1716
Published
2008-01-00
Pages
19-28
Language
English
Region
England
NLM ID
101262545
Subset
IM
Grants
NCI NIH HHS · T32 CA009302 · United States
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