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Bioactive Molecules against Rheumatoid Arthritis by Suppressing Pyroptosis

Rheumatoid arthritis is an inflammatory disease, and pyroptosis is a form of death associated with an inflammatory response. Pyroptosis, which occurs in synovial and osteoblastic cells, can exacerbate the development of rheumatoid arthritis. The inhibition of pyroptosis of these cells can, therefore...

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Detalles Bibliográficos
Autores principales: Zhou, Qian, Li, Tian, Fang, Gang, Pang, Yuzhou, Wang, Xueni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10383892/
https://www.ncbi.nlm.nih.gov/pubmed/37513864
http://dx.doi.org/10.3390/ph16070952
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author Zhou, Qian
Li, Tian
Fang, Gang
Pang, Yuzhou
Wang, Xueni
author_facet Zhou, Qian
Li, Tian
Fang, Gang
Pang, Yuzhou
Wang, Xueni
author_sort Zhou, Qian
collection PubMed
description Rheumatoid arthritis is an inflammatory disease, and pyroptosis is a form of death associated with an inflammatory response. Pyroptosis, which occurs in synovial and osteoblastic cells, can exacerbate the development of rheumatoid arthritis. The inhibition of pyroptosis of these cells can, therefore, clearly be used as a therapeutic strategy against rheumatoid arthritis. Here, we have summarized the current status of progress in the treatment of rheumatoid arthritis by targeting cellular pyroptosis. We have identified seven compounds, including a cyclic RNA, a microRNA, a peptide, and a cytokine (protein), that may influence the progression of rheumatoid arthritis by regulating the initiation of pyroptosis. All of these compounds have been shown to have anti-rheumatoid effects in vitro and/or in vivo and have the potential to be developed as anti-rheumatoid agents. These findings may help to accelerate the development of anti-rheumatoid arthritis drugs.
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spelling pubmed-103838922023-07-30 Bioactive Molecules against Rheumatoid Arthritis by Suppressing Pyroptosis Zhou, Qian Li, Tian Fang, Gang Pang, Yuzhou Wang, Xueni Pharmaceuticals (Basel) Review Rheumatoid arthritis is an inflammatory disease, and pyroptosis is a form of death associated with an inflammatory response. Pyroptosis, which occurs in synovial and osteoblastic cells, can exacerbate the development of rheumatoid arthritis. The inhibition of pyroptosis of these cells can, therefore, clearly be used as a therapeutic strategy against rheumatoid arthritis. Here, we have summarized the current status of progress in the treatment of rheumatoid arthritis by targeting cellular pyroptosis. We have identified seven compounds, including a cyclic RNA, a microRNA, a peptide, and a cytokine (protein), that may influence the progression of rheumatoid arthritis by regulating the initiation of pyroptosis. All of these compounds have been shown to have anti-rheumatoid effects in vitro and/or in vivo and have the potential to be developed as anti-rheumatoid agents. These findings may help to accelerate the development of anti-rheumatoid arthritis drugs. MDPI 2023-07-03 /pmc/articles/PMC10383892/ /pubmed/37513864 http://dx.doi.org/10.3390/ph16070952 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Zhou, Qian
Li, Tian
Fang, Gang
Pang, Yuzhou
Wang, Xueni
Bioactive Molecules against Rheumatoid Arthritis by Suppressing Pyroptosis
title Bioactive Molecules against Rheumatoid Arthritis by Suppressing Pyroptosis
title_full Bioactive Molecules against Rheumatoid Arthritis by Suppressing Pyroptosis
title_fullStr Bioactive Molecules against Rheumatoid Arthritis by Suppressing Pyroptosis
title_full_unstemmed Bioactive Molecules against Rheumatoid Arthritis by Suppressing Pyroptosis
title_short Bioactive Molecules against Rheumatoid Arthritis by Suppressing Pyroptosis
title_sort bioactive molecules against rheumatoid arthritis by suppressing pyroptosis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10383892/
https://www.ncbi.nlm.nih.gov/pubmed/37513864
http://dx.doi.org/10.3390/ph16070952
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