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Pharmaceutical therapeutics for articular regeneration and restoration: state-of-the-art technology for screening small molecular drugs

Articular cartilage damage caused by sports injury or osteoarthritis (OA) has gained increased attention as a worldwide health burden. Pharmaceutical treatments are considered cost-effective means of promoting cartilage regeneration, but are limited by their inability to generate sufficient function...

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Autores principales: Chen, Yishan, Sun, Heng, Yao, Xudong, Yu, Yeke, Tian, Tian, Xu, Weiyang, Zhou, Yujie, Ouyang, Hongwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593173/
https://www.ncbi.nlm.nih.gov/pubmed/34783870
http://dx.doi.org/10.1007/s00018-021-03983-8
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author Chen, Yishan
Sun, Heng
Yao, Xudong
Yu, Yeke
Tian, Tian
Xu, Weiyang
Zhou, Yujie
Ouyang, Hongwei
author_facet Chen, Yishan
Sun, Heng
Yao, Xudong
Yu, Yeke
Tian, Tian
Xu, Weiyang
Zhou, Yujie
Ouyang, Hongwei
author_sort Chen, Yishan
collection PubMed
description Articular cartilage damage caused by sports injury or osteoarthritis (OA) has gained increased attention as a worldwide health burden. Pharmaceutical treatments are considered cost-effective means of promoting cartilage regeneration, but are limited by their inability to generate sufficient functional chondrocytes and modify disease progression. Small molecular chemical compounds are an abundant source of new pharmaceutical therapeutics for cartilage regeneration, as they have advantages in design, fabrication, and application, and, when used in combination, act as powerful tools for manipulating cellular fate. In this review, we present current achievements in the development of small molecular drugs for cartilage regeneration, particularly in the fields of chondrocyte generation and reversion of chondrocyte degenerative phenotypes. Several clinically or preclinically available small molecules, which have been shown to facilitate chondrogenesis, chondrocyte dedifferentiation, and cellular reprogramming, and subsequently ameliorate cartilage degeneration by targeting inflammation, matrix degradation, metabolism, and epigenetics, are summarized. Notably, this review introduces essential parameters for high-throughput screening strategies, including models of different chondrogenic cell sources, phenotype readout methodologies, and transferable advanced systems from other fields. Overall, this review provides new insights into future pharmaceutical therapies for cartilage regeneration.
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spelling pubmed-85931732021-11-16 Pharmaceutical therapeutics for articular regeneration and restoration: state-of-the-art technology for screening small molecular drugs Chen, Yishan Sun, Heng Yao, Xudong Yu, Yeke Tian, Tian Xu, Weiyang Zhou, Yujie Ouyang, Hongwei Cell Mol Life Sci Review Articular cartilage damage caused by sports injury or osteoarthritis (OA) has gained increased attention as a worldwide health burden. Pharmaceutical treatments are considered cost-effective means of promoting cartilage regeneration, but are limited by their inability to generate sufficient functional chondrocytes and modify disease progression. Small molecular chemical compounds are an abundant source of new pharmaceutical therapeutics for cartilage regeneration, as they have advantages in design, fabrication, and application, and, when used in combination, act as powerful tools for manipulating cellular fate. In this review, we present current achievements in the development of small molecular drugs for cartilage regeneration, particularly in the fields of chondrocyte generation and reversion of chondrocyte degenerative phenotypes. Several clinically or preclinically available small molecules, which have been shown to facilitate chondrogenesis, chondrocyte dedifferentiation, and cellular reprogramming, and subsequently ameliorate cartilage degeneration by targeting inflammation, matrix degradation, metabolism, and epigenetics, are summarized. Notably, this review introduces essential parameters for high-throughput screening strategies, including models of different chondrogenic cell sources, phenotype readout methodologies, and transferable advanced systems from other fields. Overall, this review provides new insights into future pharmaceutical therapies for cartilage regeneration. Springer International Publishing 2021-11-16 2021 /pmc/articles/PMC8593173/ /pubmed/34783870 http://dx.doi.org/10.1007/s00018-021-03983-8 Text en © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Review
Chen, Yishan
Sun, Heng
Yao, Xudong
Yu, Yeke
Tian, Tian
Xu, Weiyang
Zhou, Yujie
Ouyang, Hongwei
Pharmaceutical therapeutics for articular regeneration and restoration: state-of-the-art technology for screening small molecular drugs
title Pharmaceutical therapeutics for articular regeneration and restoration: state-of-the-art technology for screening small molecular drugs
title_full Pharmaceutical therapeutics for articular regeneration and restoration: state-of-the-art technology for screening small molecular drugs
title_fullStr Pharmaceutical therapeutics for articular regeneration and restoration: state-of-the-art technology for screening small molecular drugs
title_full_unstemmed Pharmaceutical therapeutics for articular regeneration and restoration: state-of-the-art technology for screening small molecular drugs
title_short Pharmaceutical therapeutics for articular regeneration and restoration: state-of-the-art technology for screening small molecular drugs
title_sort pharmaceutical therapeutics for articular regeneration and restoration: state-of-the-art technology for screening small molecular drugs
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593173/
https://www.ncbi.nlm.nih.gov/pubmed/34783870
http://dx.doi.org/10.1007/s00018-021-03983-8
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