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Therapy-Induced Senescence in Cancer

Jonathan A. Ewald, Joshua A. Desotelle, George Wilding, David F. Jarrard

JNCI Journal of the National Cancer Institute · 2010 · ▲ 822 citations

Abstract

Cellular senescence(definition) is a response to nonlethal stress that results in persistent cytostasis with a distinct morphological and biochemical phenotype. The senescence phenotype, detected in tumors through the expression of mRNA and protein markers, can be generated in cancer cells lacking functional p53 and retinoblastoma protein. Current research suggests that therapy-induced senescence (TIS) represents a novel functional target that may improve cancer therapy. TIS can be induced in immortal and transformed cancer cells by selected anticancer compounds or radiation, and accumulating data indicate that TIS may produce reduced toxicity-related side effects and increased tumor-specific immune activity. This review examines the current status of TIS-regulated mechanisms, agents, and senescence biomarkers with the goal of encouraging further development of this approach to cancer therapy. Remaining hurdles include the lack of efficient senescence-inducing agents and incomplete biological data on tumor response. The identification of additional compounds and other targeted approaches to senescence induction will further the development of TIS in the clinical treatment of cancer.

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Provenance

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OpenAlex
DOI
10.1093/jnci/djq364
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2026-05-31 MST

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APA
Ewald, J.A., Desotelle, J.A., Wilding, G., &amp; Jarrard, D.F. (2010). Therapy-Induced Senescence in Cancer. <em>JNCI Journal of the National Cancer Institute</em>. https://doi.org/10.1093/jnci/djq364
Vancouver
Ewald JA, Desotelle JA, Wilding G, Jarrard DF. Therapy-Induced Senescence in Cancer. JNCI Journal of the National Cancer Institute. 2010. doi:10.1093/jnci/djq364.
BibTeX
@article{jonathan2010Therap, title = {Therapy-Induced Senescence in Cancer}, author = {Jonathan A. Ewald and Joshua A. Desotelle and George Wilding and David F. Jarrard}, journal = {JNCI Journal of the National Cancer Institute}, year = {2010}, doi = {10.1093/jnci/djq364}, }

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