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The emerging and diverse roles of sirtuins in cancer: a clinical perspective

Wenyong Chen, Hongfeng Yuan, Leila Su

OncoTargets and Therapy · 2013 · ▲ 162 citations

Abstract

Sirtuins are a highly conserved family of nicotinamide adenine dinucleotide (NAD(+))-dependent protein lysine modifying enzymes with deacetylase, adenosine diphosphateribosyltransferase and other deacylase activities. Mammals have seven sirtuins, namely SIRT1-7. They are key regulators for a wide variety of cellular and physiological processes such as cell proliferation, differentiation, DNA damage and stress response, genome stability, cell survival, metabolism, energy homeostasis, organ development, aging, and cancer. Here we present an extensive literature review of the roles of mammalian sirtuins, particularly SIRT1 as that is the most studied sirtuin, in human epithelial, neuronal, hematopoietic, and mesenchymal malignancies, covering breast, prostate, lung, thyroid, liver, colon, gastric, pancreatic, ovarian, and cervical cancers, tumors of the central nervous system, leukemia and lymphoma, and soft tissue sarcomas. Collective evidence suggests sirtuins are involved in both promoting and suppressing tumorigenesis depending on cellular and molecular contexts. We discuss the potential use of sirtuin modulators, especially sirtuin inhibitors, in cancer treatment.

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Provenance

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OpenAlex
DOI
10.2147/ott.s37750
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2026-10-23 MST

Cite this

APA
Chen, W., Yuan, H., &amp; Su, L. (2013). The emerging and diverse roles of sirtuins in cancer: a clinical perspective. <em>OncoTargets and Therapy</em>. https://doi.org/10.2147/ott.s37750
Vancouver
Chen W, Yuan H, Su L. The emerging and diverse roles of sirtuins in cancer: a clinical perspective. OncoTargets and Therapy. 2013. doi:10.2147/ott.s37750.
BibTeX
@article{wenyong2013Theeme, title = {The emerging and diverse roles of sirtuins in cancer: a clinical perspective}, author = {Wenyong Chen and Hongfeng Yuan and Leila Su}, journal = {OncoTargets and Therapy}, year = {2013}, doi = {10.2147/ott.s37750}, }

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