Related Experiment Video
Updated: Apr 19, 2026

Deacetylation Assays to Unravel the Interplay between Sirtuins SIRT2 and Specific Protein-substrates
Published on: February 27, 2016
Anticancer agents targeted to sirtuins
Tomohiro Kozako1, Takayoshi Suzuki2, Makoto Yoshimitsu3
1Department of Biochemistry, Faculty of Pharmaceutical Sciences, Fukuoka University, 8-19-1 Nanakuma, Jonan-ku, Fukuoka 814-0180, Japan. kozako@fukuoka-u.ac.jp.
Abstract:
Sirtuins are nicotinamide adenine dinucleotide+-dependent deacetylases of which there are seven isoforms (SIRT1-7). Sirtuin activity is linked to gene expression, lifespan extension, neurodegeneration, and age-related disorders. Numerous studies have suggested that sirtuins could be of great significance with regard to both antiaging and tumorigenesis, depending on its targets in specific signaling pathways or in specific cancers. Recent studies have identified small chemical compounds that modulate sirtuins, and these modulators have enabled a greater understanding of the biological function and molecular mechanisms of sirtuins. This review highlights the possibility of sirtuins, especially SIRT1 and SIRT2, for cancer therapy targets, and focuses on the therapeutic potential of sirtuin modulators both in cancer prevention and treatment.
Insights
Sirtuins (silent information regulators) are enzymes impacting aging and cancer. This review explores sirtuin modulators as potential cancer therapies, focusing on SIRT1 and SIRT2.
Area of Science:
- Biochemistry and Molecular Biology
- Oncology
- Aging Research
Background:
- Sirtuins are a class of nicotinamide adenine dinucleotide+-dependent deacetylases with seven isoforms (SIRT1-7).
- Sirtuin activity influences critical cellular processes including gene expression, aging, and neurodegeneration.
- Emerging evidence links sirtuins to both anti-aging effects and cancer development, contingent on specific cellular targets and pathways.
Purpose of the Study:
- To review the role of sirtuins, particularly SIRT1 and SIRT2, as potential therapeutic targets in cancer.
- To explore the therapeutic potential of small molecule sirtuin modulators in cancer prevention and treatment.
- To enhance understanding of sirtuin biological functions and molecular mechanisms through modulator studies.
Main Methods:
- Literature review of studies investigating sirtuin isoforms (SIRT1-7) and their functions.
- Analysis of research on small chemical compounds that modulate sirtuin activity.
- Focus on studies examining the link between sirtuins, particularly SIRT1 and SIRT2, and cancer.
Main Results:
- Sirtuin activity is implicated in diverse biological processes, including aging and age-related diseases.
- Sirtuins play a dual role in tumorigenesis, potentially promoting or inhibiting cancer depending on context.
- Sirtuin modulators have proven valuable in elucidating sirtuin functions and mechanisms.
Conclusions:
- Sirtuins, especially SIRT1 and SIRT2, represent promising targets for novel cancer therapies.
- Sirtuin modulators offer significant therapeutic potential for both the prevention and treatment of cancer.
- Further research into sirtuin modulators could lead to innovative anti-cancer strategies.
More Related Videos
06:00Through the Looking Glass: Time-lapse Microscopy and Longitudinal Tracking of Single Cells to Study Anti-cancer Therapeutics
Published on: May 14, 2016
07:48Utilizing Functional Genomics Screening to Identify Potentially Novel Drug Targets in Cancer Cell Spheroid Cultures
Published on: December 26, 2016
Related Concept Videos
Targeted Cancer Therapies
There are several types of targeted therapies against...
Targeted Cancer Therapies
siRNA - Small Interfering RNAs
In the cytoplasm, siRNA is processed from a double-stranded RNA, which comes from either endogenous DNA transcription or exogenous sources like a virus. This double-stranded RNA is then cleaved by the...
Inhibition of Cdk Activity
Electron Transport Chain: Complex I and II
ROS generation is regulated and maintained at moderate levels necessary...
mTOR Signaling and Cancer Progression
The mTOR pathway or the...