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DKK1抑制剂的药物研发

Drug Discovery of DKK1 Inhibitors.

作者信息

Jiang Hewen, Zhang Zongkang, Yu Yuanyuan, Chu Hang Yin, Yu Sifan, Yao Shanshan, Zhang Ge, Zhang Bao-Ting

机构信息

School of Chinese Medicine, Chinese University of Hong Kong, Hong Kong, China.

Guangdong-Hong Kong Macao Greater Bay Area International Research Platform for Aptamer-Based Translational Medicine and Drug Discovery, Hong Kong, China.

出版信息

Front Pharmacol. 2022 Mar 9;13:847387. doi: 10.3389/fphar.2022.847387. eCollection 2022.

DOI:10.3389/fphar.2022.847387
PMID:35355709
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8959454/
Abstract

Dickkopf-1 (DKK1) is a well-characterized Wnt inhibitor and component of the Wnt/β-catenin signaling pathway, whose dysregulation is associated with multiple abnormal pathologies including osteoporosis, Alzheimer's disease, diabetes, and various cancers. The Wnt signaling pathway has fundamental roles in cell fate determination, cell proliferation, and survival; thus, its mis-regulation can lead to disease. Although DKK1 is involved in other signaling pathways, including the β-catenin-independent Wnt pathway and the DKK1/CKAP4 pathway, the inhibition of DKK1 to propagate Wnt/β-catenin signals has been validated as an effective way to treat related diseases. In fact, strategies for developing DKK1 inhibitors have produced encouraging clinical results in different pathological models, and many publications provide detailed information about these inhibitors, which include small molecules, antibodies, and nucleic acids, and may function at the protein or mRNA level. However, no systematic review has yet provided an overview of the various aspects of their development and prospects. Therefore, we review the DKK1 inhibitors currently available or under study and provide an outlook on future studies involving DKK1 and drug discovery.

摘要

Dickkopf-1(DKK1)是一种特征明确的Wnt抑制剂,也是Wnt/β-连环蛋白信号通路的组成部分,其失调与多种异常病理状况相关,包括骨质疏松症、阿尔茨海默病、糖尿病和各种癌症。Wnt信号通路在细胞命运决定、细胞增殖和存活中起基本作用;因此,其调节异常会导致疾病。尽管DKK1参与其他信号通路,包括不依赖β-连环蛋白的Wnt通路和DKK1/CKAP4通路,但抑制DKK1以传导Wnt/β-连环蛋白信号已被证实是治疗相关疾病的有效方法。事实上,开发DKK1抑制剂的策略在不同病理模型中已产生令人鼓舞的临床结果,许多出版物提供了有关这些抑制剂的详细信息,这些抑制剂包括小分子、抗体和核酸,可能在蛋白质或mRNA水平发挥作用。然而,尚无系统综述对其开发和前景的各个方面进行概述。因此,我们综述了目前可用或正在研究的DKK1抑制剂,并对涉及DKK1和药物发现的未来研究进行展望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cc4/8959454/3bbd0434717b/fphar-13-847387-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cc4/8959454/7b589249c8d2/fphar-13-847387-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cc4/8959454/7a64b45ccb9d/fphar-13-847387-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cc4/8959454/3bbd0434717b/fphar-13-847387-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cc4/8959454/7b589249c8d2/fphar-13-847387-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cc4/8959454/7a64b45ccb9d/fphar-13-847387-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cc4/8959454/3bbd0434717b/fphar-13-847387-g003.jpg

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