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Small-Molecule PROTACs for Cancer Immunotherapy

Unsatisfactory physicochemical properties of macromolecular drugs seriously hinder their application in tumor immunotherapy. However, these problems can be effectively solved by small-molecule compounds. In the promising field of small-molecule drug development, proteolysis targeting chimera (PROTAC...

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Detalles Bibliográficos
Autores principales: Liu, Zefan, Zhang, Yajun, Xiang, Yucheng, Kang, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458232/
https://www.ncbi.nlm.nih.gov/pubmed/36080223
http://dx.doi.org/10.3390/molecules27175439
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author Liu, Zefan
Zhang, Yajun
Xiang, Yucheng
Kang, Xin
author_facet Liu, Zefan
Zhang, Yajun
Xiang, Yucheng
Kang, Xin
author_sort Liu, Zefan
collection PubMed
description Unsatisfactory physicochemical properties of macromolecular drugs seriously hinder their application in tumor immunotherapy. However, these problems can be effectively solved by small-molecule compounds. In the promising field of small-molecule drug development, proteolysis targeting chimera (PROTAC) offers a novel mode of action in the interactions between small molecules and therapeutic targets (mainly proteins). This revolutionary technology has shown considerable impact on several proteins related to tumor survival but is rarely exploited in proteins associated with immuno-oncology up until now. This review attempts to comprehensively summarize the well-studied and less-developed immunological targets available for PROTAC technology, as well as some targets to be explored, aiming to provide more options and opportunities for the development of small-molecule-based tumor immunotherapy. In addition, some novel directions that can magnify and broaden the protein degradation efficiency are mentioned to improve PROTAC design in the future.
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spelling pubmed-94582322022-09-09 Small-Molecule PROTACs for Cancer Immunotherapy Liu, Zefan Zhang, Yajun Xiang, Yucheng Kang, Xin Molecules Review Unsatisfactory physicochemical properties of macromolecular drugs seriously hinder their application in tumor immunotherapy. However, these problems can be effectively solved by small-molecule compounds. In the promising field of small-molecule drug development, proteolysis targeting chimera (PROTAC) offers a novel mode of action in the interactions between small molecules and therapeutic targets (mainly proteins). This revolutionary technology has shown considerable impact on several proteins related to tumor survival but is rarely exploited in proteins associated with immuno-oncology up until now. This review attempts to comprehensively summarize the well-studied and less-developed immunological targets available for PROTAC technology, as well as some targets to be explored, aiming to provide more options and opportunities for the development of small-molecule-based tumor immunotherapy. In addition, some novel directions that can magnify and broaden the protein degradation efficiency are mentioned to improve PROTAC design in the future. MDPI 2022-08-25 /pmc/articles/PMC9458232/ /pubmed/36080223 http://dx.doi.org/10.3390/molecules27175439 Text en © 2022 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
Liu, Zefan
Zhang, Yajun
Xiang, Yucheng
Kang, Xin
Small-Molecule PROTACs for Cancer Immunotherapy
title Small-Molecule PROTACs for Cancer Immunotherapy
title_full Small-Molecule PROTACs for Cancer Immunotherapy
title_fullStr Small-Molecule PROTACs for Cancer Immunotherapy
title_full_unstemmed Small-Molecule PROTACs for Cancer Immunotherapy
title_short Small-Molecule PROTACs for Cancer Immunotherapy
title_sort small-molecule protacs for cancer immunotherapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458232/
https://www.ncbi.nlm.nih.gov/pubmed/36080223
http://dx.doi.org/10.3390/molecules27175439
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