YZL-51N functions as a selective inhibitor of SIRT7 by NAD+ competition to impede DNA damage repair

  • iScience. 2024 May 16;27(6):110014. doi: 10.1016/j.isci.2024.110014.
Tian-Shu Kang  1 Yong-Ming Yan  1 Yuan Tian  1  2 Jun Zhang  1  2 Minghui Zhang  1 Yuxin Shu  1 Jinbo Huang  1 Jing He  1 Cheng-Tian Tao  1 Qian Zhu  1  2 Jinke Gu  1 Xiaopeng Lu  1  2 Yong-Xian Cheng  1  2 Wei-Guo Zhu  1  2
Affiliations
  • 1. International Cancer Center, Department of Biochemistry and Molecular Biology, Institute for Inheritance-Based Innovation of Chinese Medicine, School of Pharmaceutical Sciences, Shenzhen University Medical School, Shenzhen 518055, China.
  • 2. Department Guangdong Key Laboratory of Genome Instability and Human Disease Prevention, Marshall Laboratory of Biomedical Engineering, Shenzhen University Medical School, Shenzhen 518055, China.
Abstract

The NAD+-dependent deacetylase SIRT7 is a pivotal regulator of DNA damage response (DDR) and a promising drug target for developing Cancer therapeutics. However, limited progress has been made in SIRT7 modulator discovery. Here, we applied peptide-based deacetylase platforms for SIRT7 enzymatic evaluation and successfully identified a potent SIRT7 Inhibitor YZL-51N. We initially isolated bioactive YZL-51N from cockroach (Periplaneta americana) extracts and then developed the de novo synthesis of this compound. Further investigation revealed that YZL-51N impaired SIRT7 enzymatic activities through occupation of the NAD+ binding pocket. YZL-51N attenuated DNA damage repair induced by ionizing radiation (IR) in colorectal Cancer cells and exhibited a synergistic Anticancer effect when used in combination with etoposide. Overall, our study not only identified YZL-51N as a selective SIRT7 Inhibitor from insect resources, but also confirmed its potential use in combined chemo-radiotherapy by interfering in the DNA damage repair process.

Keywords
Molecular biology experimental approach; Natural product biochemistry; Pharmacology; Small molecule.
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