Skip to content
Preprint · OA via OpenAlex

Aging, Cellular Senescence, and Cancer

Judith Campisi

Annual Review of Physiology · 2012 · ▲ 2,890 citations

Abstract

For most species, aging promotes a host of degenerative pathologies that are characterized by debilitating losses of tissue or cellular function. However, especially among vertebrates, aging also promotes hyperplastic pathologies, the most deadly of which is cancer. In contrast to the loss of function that characterizes degenerating cells and tissues, malignant (cancerous) cells must acquire new (albeit aberrant) functions that allow them to develop into a lethal tumor. This review discusses the idea that, despite seemingly opposite characteristics, the degenerative and hyperplastic pathologies of aging are at least partly linked by a common biological phenomenon: a cellular stress response known as cellular senescence(definition). The senescence response is widely recognized as a potent tumor suppressive mechanism. However, recent evidence strengthens the idea that it also drives both degenerative and hyperplastic pathologies, most likely by promoting chronic inflammation. Thus, the senescence response may be the result of antagonistically pleiotropic gene action.

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

Read at source →

Provenance

Source
OpenAlex
DOI
10.1146/annurev-physiol-030212-183653
Canonical
link ↗
Fetched
2026-05-31 MST

Cite this

APA
Campisi, J. (2012). Aging, Cellular Senescence, and Cancer. <em>Annual Review of Physiology</em>. https://doi.org/10.1146/annurev-physiol-030212-183653
Vancouver
Campisi J. Aging, Cellular Senescence, and Cancer. Annual Review of Physiology. 2012. doi:10.1146/annurev-physiol-030212-183653.
BibTeX
@unpublished{judith2012AgingC, title = {Aging, Cellular Senescence, and Cancer}, author = {Judith Campisi}, journal = {Annual Review of Physiology}, year = {2012}, doi = {10.1146/annurev-physiol-030212-183653}, }

Research neighborhood

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

Related findings