Selective inhibition of SIRT2: A disputable therapeutic approach in cancer therapy

被引:11
|
作者
Kaya, Selen Gozde [1 ]
Eren, Gokcen [1 ]
机构
[1] Gazi Univ, Fac Pharm, Dept Pharmaceut Chem, SIRTeam Grp, TR-06330 Ankara, Turkiye
关键词
Sirtuin; SIRT2; Selectivity; Antitumor; Cancer; TUMOR-SUPPRESSOR; STRUCTURAL BASIS; SIRT2-MEDIATED DEACETYLATION; HEPATOCELLULAR-CARCINOMA; CRYSTAL-STRUCTURE; DOWN-REGULATION; CELL-GROWTH; DISCOVERY; SIRTUINS; PROMOTES;
D O I
10.1016/j.bioorg.2023.107038
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sirtuin 2 (SIRT2) is involved in a wide range of processes, from transcription to metabolism to genome stability. Dysregulation of SIRT2 has been associated with the pathogenesis and progression of different diseases, such as cancer and neurodegenerative disorders. In this context, targeting SIRT2 activity by small molecule inhibitors is a promising therapeutic strategy for treating related conditions, particularly cancer. This review summarizes the regulatory roles and molecular mechanisms of SIRT2 in cancer and the attempts to evaluate potential antitumor activities of SIRT2-selective inhibitors by in vitro and in vivo testing, which are expected to deepen our understanding of the role of SIRT2 in tumorigenesis and progression and may offer important clues or inspiration ideas for developing SIRT2 inhibitors with excellent affinity and selectivity.
引用
收藏
页数:14
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