开发基于天然产物的靶向蛋白质降解剂作为抗癌剂。

IF 4.5 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Bioorganic Chemistry Pub Date : 2024-09-02 DOI:10.1016/j.bioorg.2024.107772
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引用次数: 0

摘要

靶向蛋白质降解(TPD)已成为一种通过 "事件驱动 "药理学模式消除致癌蛋白质的有效方法。蛋白水解靶向嵌合体(PROTACs)、分子胶(MGs)和疏水标记(HyTing)已发展成为三大类靶向蛋白降解技术。天然产物(NPs)是抗癌药物的主要来源,在 TPD 技术的发展中发挥了重要作用。NPs 可提供各种 E3 配体、感兴趣的蛋白质 (POI) 弹头和疏水标签 (HyTs),从而潜在地扩展了 TPD 工具箱。作为 TPD 领域的一个有前途的方向,基于 NP 的降解剂已在抗癌治疗中显示出巨大的潜力。在这篇综述中,我们总结了在开发具有抗癌应用价值的 NP 基降解剂(PROTACs、MGs 和 HyTing)方面的最新进展。此外,我们还提出了未来由 NPs 衍生的靶向蛋白质降解剂所面临的挑战,同时也提出了潜在的机遇。
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Development of natural product-based targeted protein degraders as anticancer agents

Targeted protein degradation (TPD) has emerged as a powerful approach for eliminating cancer-causing proteins through an “event-driven” pharmacological mode. Proteolysis-targeting chimeras (PROTACs), molecular glues (MGs), and hydrophobic tagging (HyTing) have evolved into three major classes of TPD technologies. Natural products (NPs) are a primary source of anticancer drugs and have played important roles in the development of TPD technology. NPs potentially expand the toolbox of TPD by providing a variety of E3 ligase ligands, protein of interest (POI) warheads, and hydrophobic tags (HyTs). As a promising direction in the TPD field, NP-based degraders have shown great potential for anticancer therapy. In this review, we summarize recent advances in the development of NP-based degraders (PROTACs, MGs and HyTing) with anticancer applications. Moreover, we put forward the challenges while presenting potential opportunities for the advancement of future targeted protein degraders derived from NPs.

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来源期刊
Bioorganic Chemistry
Bioorganic Chemistry 生物-生化与分子生物学
CiteScore
9.70
自引率
3.90%
发文量
679
审稿时长
31 days
期刊介绍: Bioorganic Chemistry publishes research that addresses biological questions at the molecular level, using organic chemistry and principles of physical organic chemistry. The scope of the journal covers a range of topics at the organic chemistry-biology interface, including: enzyme catalysis, biotransformation and enzyme inhibition; nucleic acids chemistry; medicinal chemistry; natural product chemistry, natural product synthesis and natural product biosynthesis; antimicrobial agents; lipid and peptide chemistry; biophysical chemistry; biological probes; bio-orthogonal chemistry and biomimetic chemistry. For manuscripts dealing with synthetic bioactive compounds, the Journal requires that the molecular target of the compounds described must be known, and must be demonstrated experimentally in the manuscript. For studies involving natural products, if the molecular target is unknown, some data beyond simple cell-based toxicity studies to provide insight into the mechanism of action is required. Studies supported by molecular docking are welcome, but must be supported by experimental data. The Journal does not consider manuscripts that are purely theoretical or computational in nature. The Journal publishes regular articles, short communications and reviews. Reviews are normally invited by Editors or Editorial Board members. Authors of unsolicited reviews should first contact an Editor or Editorial Board member to determine whether the proposed article is within the scope of the Journal.
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