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PROTAC: An Effective Targeted Protein Degradation Strategy for Cancer Therapy

Proteolysis targeting chimeric (PROTAC) technology is an effective endogenous protein degradation tool developed in recent years that can ubiquitinate the target proteins through the ubiquitin-proteasome system (UPS) to achieve an effect on tumor growth. A number of literature studies on PROTAC tech...

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Autores principales: Qi, Si-Min, Dong, Jinyun, Xu, Zhi-Yuan, Cheng, Xiang-Dong, Zhang, Wei-Dong, Qin, Jiang-Jiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8138175/
https://www.ncbi.nlm.nih.gov/pubmed/34025443
http://dx.doi.org/10.3389/fphar.2021.692574
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author Qi, Si-Min
Dong, Jinyun
Xu, Zhi-Yuan
Cheng, Xiang-Dong
Zhang, Wei-Dong
Qin, Jiang-Jiang
author_facet Qi, Si-Min
Dong, Jinyun
Xu, Zhi-Yuan
Cheng, Xiang-Dong
Zhang, Wei-Dong
Qin, Jiang-Jiang
author_sort Qi, Si-Min
collection PubMed
description Proteolysis targeting chimeric (PROTAC) technology is an effective endogenous protein degradation tool developed in recent years that can ubiquitinate the target proteins through the ubiquitin-proteasome system (UPS) to achieve an effect on tumor growth. A number of literature studies on PROTAC technology have proved an insight into the feasibility of PROTAC technology to degrade target proteins. Additionally, the first oral PROTACs (ARV-110 and ARV-471) have shown encouraging results in clinical trials for prostate and breast cancer treatment, which inspires a greater enthusiasm for PROTAC research. Here we focus on the structures and mechanisms of PROTACs and describe several classes of effective PROTAC degraders based on E3 ligases.
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spelling pubmed-81381752021-05-22 PROTAC: An Effective Targeted Protein Degradation Strategy for Cancer Therapy Qi, Si-Min Dong, Jinyun Xu, Zhi-Yuan Cheng, Xiang-Dong Zhang, Wei-Dong Qin, Jiang-Jiang Front Pharmacol Pharmacology Proteolysis targeting chimeric (PROTAC) technology is an effective endogenous protein degradation tool developed in recent years that can ubiquitinate the target proteins through the ubiquitin-proteasome system (UPS) to achieve an effect on tumor growth. A number of literature studies on PROTAC technology have proved an insight into the feasibility of PROTAC technology to degrade target proteins. Additionally, the first oral PROTACs (ARV-110 and ARV-471) have shown encouraging results in clinical trials for prostate and breast cancer treatment, which inspires a greater enthusiasm for PROTAC research. Here we focus on the structures and mechanisms of PROTACs and describe several classes of effective PROTAC degraders based on E3 ligases. Frontiers Media S.A. 2021-05-07 /pmc/articles/PMC8138175/ /pubmed/34025443 http://dx.doi.org/10.3389/fphar.2021.692574 Text en Copyright © 2021 Qi, Dong, Xu, Cheng, Zhang and Qin. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Qi, Si-Min
Dong, Jinyun
Xu, Zhi-Yuan
Cheng, Xiang-Dong
Zhang, Wei-Dong
Qin, Jiang-Jiang
PROTAC: An Effective Targeted Protein Degradation Strategy for Cancer Therapy
title PROTAC: An Effective Targeted Protein Degradation Strategy for Cancer Therapy
title_full PROTAC: An Effective Targeted Protein Degradation Strategy for Cancer Therapy
title_fullStr PROTAC: An Effective Targeted Protein Degradation Strategy for Cancer Therapy
title_full_unstemmed PROTAC: An Effective Targeted Protein Degradation Strategy for Cancer Therapy
title_short PROTAC: An Effective Targeted Protein Degradation Strategy for Cancer Therapy
title_sort protac: an effective targeted protein degradation strategy for cancer therapy
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8138175/
https://www.ncbi.nlm.nih.gov/pubmed/34025443
http://dx.doi.org/10.3389/fphar.2021.692574
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