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SIRT6 调节剂的新兴治疗潜力。

Emerging Therapeutic Potential of SIRT6 Modulators.

机构信息

Department of Chemistry, University of Oxford, South Parks Road, Oxford OX1 3QZ, United Kingdom.

Department of Drug Chemistry & Technologies, Sapienza University of Rome, P.le A Moro 5, 00185 Rome, Italy.

出版信息

J Med Chem. 2021 Jul 22;64(14):9732-9758. doi: 10.1021/acs.jmedchem.1c00601. Epub 2021 Jul 2.

Abstract

Sirtuin 6 (SIRT6) is an NAD-dependent protein deacylase and mono-ADP-ribosyltransferase of the sirtuin family with a wide substrate specificity. and studies have indicated that SIRT6 overexpression or activation has beneficial effects for cellular processes such as DNA repair, metabolic regulation, and aging. On the other hand, SIRT6 has contrasting roles in cancer, acting either as a tumor suppressor or promoter in a context-specific manner. Given its central role in cellular homeostasis, SIRT6 has emerged as a promising target for the development of small-molecule activators and inhibitors possessing a therapeutic potential in diseases ranging from cancer to age-related disorders. Moreover, specific modulators allow the molecular details of SIRT6 activity to be scrutinized and further validate the enzyme as a pharmacological target. In this Perspective, we summarize the current knowledge about SIRT6 pharmacology and medicinal chemistry and describe the features of the activators and inhibitors identified so far.

摘要

Sirtuin 6(SIRT6)是一种 NAD 依赖性蛋白脱酰基酶和单 ADP-核糖基转移酶,属于 sirtuin 家族,具有广泛的底物特异性。研究表明,SIRT6 的过表达或激活对细胞过程具有有益的影响,如 DNA 修复、代谢调节和衰老。另一方面,SIRT6 在癌症中具有相反的作用,以特定于上下文的方式作为肿瘤抑制因子或促进因子发挥作用。鉴于其在细胞内稳态中的核心作用,SIRT6 已成为小分子激活剂和抑制剂开发的有前途的靶点,这些激活剂和抑制剂在从癌症到与年龄相关的疾病等疾病中具有治疗潜力。此外,特定的调节剂可以仔细研究 SIRT6 活性的分子细节,并进一步验证该酶作为药理学靶点的合理性。在本观点中,我们总结了 SIRT6 药理学和药物化学的最新知识,并描述了迄今为止鉴定的激活剂和抑制剂的特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b15f/8389836/baf12015e1e9/jm1c00601_0001.jpg

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