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IκB kinase β (IKKβ): Structure, transduction mechanism, biological function, and discovery of its inhibitors
The effective approach to discover innovative drugs will ask natural products for answers because of their complex and changeable structures and multiple biological activities. Inhibitory kappa B kinase beta (IKKβ), known as IKK2, is a key regulatory kinase responsible for the activation of NF-κB th...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10496512/ https://www.ncbi.nlm.nih.gov/pubmed/37705738 http://dx.doi.org/10.7150/ijbs.85158 |
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author | Zhang, Juan Zhang, Rui Li, Wei Ma, Xiao-Chi Qiu, Feng Sun, Cheng-Peng |
author_facet | Zhang, Juan Zhang, Rui Li, Wei Ma, Xiao-Chi Qiu, Feng Sun, Cheng-Peng |
author_sort | Zhang, Juan |
collection | PubMed |
description | The effective approach to discover innovative drugs will ask natural products for answers because of their complex and changeable structures and multiple biological activities. Inhibitory kappa B kinase beta (IKKβ), known as IKK2, is a key regulatory kinase responsible for the activation of NF-κB through its phosphorylation at Ser177 and Ser181 to promote the phosphorylation of inhibitors of kappa B (IκBs), triggering their ubiquitination and degradation to active the nuclear factor kappa-B (NF-κB) cascade. Chemical inhibition of IKKβ or its genetic knockout has become an effective method to block NF-κB-mediated proliferation and migration of tumor cells and inflammatory response. In this review, we summarized the structural feature and transduction mechanism of IKKβ and the discovery of inhibitors from natural resources (e.g. sesquiterpenoids, diterpenoids, triterpenoids, flavonoids, and alkaloids) and chemical synthesis (e.g. pyrimidines, pyridines, pyrazines, quinoxalines, thiophenes, and thiazolidines). In addition, the biosynthetic pathway of novel natural IKKβ inhibitors and their biological potentials were discussed. This review will provide inspiration for the structural modification of IKKβ inhibitors based on the skeleton of natural products or chemical synthesis and further phytochemistry investigations. |
format | Online Article Text |
id | pubmed-10496512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-104965122023-09-13 IκB kinase β (IKKβ): Structure, transduction mechanism, biological function, and discovery of its inhibitors Zhang, Juan Zhang, Rui Li, Wei Ma, Xiao-Chi Qiu, Feng Sun, Cheng-Peng Int J Biol Sci Review The effective approach to discover innovative drugs will ask natural products for answers because of their complex and changeable structures and multiple biological activities. Inhibitory kappa B kinase beta (IKKβ), known as IKK2, is a key regulatory kinase responsible for the activation of NF-κB through its phosphorylation at Ser177 and Ser181 to promote the phosphorylation of inhibitors of kappa B (IκBs), triggering their ubiquitination and degradation to active the nuclear factor kappa-B (NF-κB) cascade. Chemical inhibition of IKKβ or its genetic knockout has become an effective method to block NF-κB-mediated proliferation and migration of tumor cells and inflammatory response. In this review, we summarized the structural feature and transduction mechanism of IKKβ and the discovery of inhibitors from natural resources (e.g. sesquiterpenoids, diterpenoids, triterpenoids, flavonoids, and alkaloids) and chemical synthesis (e.g. pyrimidines, pyridines, pyrazines, quinoxalines, thiophenes, and thiazolidines). In addition, the biosynthetic pathway of novel natural IKKβ inhibitors and their biological potentials were discussed. This review will provide inspiration for the structural modification of IKKβ inhibitors based on the skeleton of natural products or chemical synthesis and further phytochemistry investigations. Ivyspring International Publisher 2023-08-06 /pmc/articles/PMC10496512/ /pubmed/37705738 http://dx.doi.org/10.7150/ijbs.85158 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Review Zhang, Juan Zhang, Rui Li, Wei Ma, Xiao-Chi Qiu, Feng Sun, Cheng-Peng IκB kinase β (IKKβ): Structure, transduction mechanism, biological function, and discovery of its inhibitors |
title | IκB kinase β (IKKβ): Structure, transduction mechanism, biological function, and discovery of its inhibitors |
title_full | IκB kinase β (IKKβ): Structure, transduction mechanism, biological function, and discovery of its inhibitors |
title_fullStr | IκB kinase β (IKKβ): Structure, transduction mechanism, biological function, and discovery of its inhibitors |
title_full_unstemmed | IκB kinase β (IKKβ): Structure, transduction mechanism, biological function, and discovery of its inhibitors |
title_short | IκB kinase β (IKKβ): Structure, transduction mechanism, biological function, and discovery of its inhibitors |
title_sort | iκb kinase β (ikkβ): structure, transduction mechanism, biological function, and discovery of its inhibitors |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10496512/ https://www.ncbi.nlm.nih.gov/pubmed/37705738 http://dx.doi.org/10.7150/ijbs.85158 |
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