Skip to content
Open access · CC-BY via OpenAlex

Cellular senescence and its effector programs

Rafik Salama, Mahito Sadaie, Matthew Hoare, Masashi Narita

Genes & Development · 2014 · ▲ 839 citations

Abstract

Cellular senescence(definition) is a stress response that accompanies stable exit from the cell cycle. Classically, senescence, particularly in human cells, involves the p53 and p16/Rb pathways, and often both of these tumor suppressor pathways need to be abrogated to bypass senescence. In parallel, a number of effector mechanisms of senescence have been identified and characterized. These studies suggest that senescence is a collective phenotype of these multiple effectors, and their intensity and combination can be different depending on triggers and cell types, conferring a complex and diverse nature to senescence. Series of studies on senescence-associated secretory phenotype (SASP) in particular have revealed various layers of functionality of senescent cells in vivo. Here we discuss some key features of senescence effectors and attempt to functionally link them when it is possible.

◌ CITATION ONLY
Full text is not openly licensed for redistribution here. Read it at the source:

Read at source →

Provenance

Source
OpenAlex
DOI
10.1101/gad.235184.113
Canonical
link ↗
Fetched
2026-05-31 MST

Cite this

APA
Salama, R., Sadaie, M., Hoare, M., &amp; Narita, M. (2014). Cellular senescence and its effector programs. <em>Genes & Development</em>. https://doi.org/10.1101/gad.235184.113
Vancouver
Salama R, Sadaie M, Hoare M, Narita M. Cellular senescence and its effector programs. Genes & Development. 2014. doi:10.1101/gad.235184.113.
BibTeX
@article{rafik2014Cellul, title = {Cellular senescence and its effector programs}, author = {Rafik Salama and Mahito Sadaie and Matthew Hoare and Masashi Narita}, journal = {Genes & Development}, year = {2014}, doi = {10.1101/gad.235184.113}, }

Research neighborhood

References, citing works, and semantically nearest findings. Click a node to open it.

Related findings