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PROTACs: great opportunities for academia and industry (an update from 2020 to 2021)
Open accessAbstract
PROteolysis TArgeting Chimeras (PROTACs) technology is a new protein-degradation strategy that has emerged in recent years. It uses bifunctional small molecules to induce the ubiquitination and degradation of target proteins through the ubiquitin–proteasome system. PROTACs can not only be used as potential clinical treatments for diseases such as cancer, immune disorders, viral infections, and neurodegenerative diseases, but also provide unique chemical knockdown tools for biological research in a catalytic, reversible, and rapid manner. In 2019, our group published a review article “PROTACs: great opportunities for academia and industry” in the journal, summarizing the representative compounds of PROTACs reported before the end of 2019. In the past 2 years, the entire field of protein degradation has experienced rapid development, including not only a large increase in the number of research papers on protein-degradation technology but also a rapid increase in the number of small-molecule degraders that have entered the clinical and will enter the clinical stage. In addition to PROTAC and molecular glue technology, other new degradation technologies are also developing rapidly. In this article, we mainly summarize and review the representative PROTACs of related targets published in 2020–2021 to present to researchers the exciting developments in the field of protein degradation. The problems that need to be solved in this field will also be briefly introduced.
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“Protein regulation can be categorized into two primary classes based on the disease mechanism: protein degradation and protein stabilization.476”
From Recent advances in targeting the “undruggable” proteins: from drug discovery to clinical trials (2023) · cites this paper as [476]
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Zhang, J., Zhang, Y., Wang, J., Xia, Y., Zhang, J., & Chen, L. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01911-3 · Cited by 1,138
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BackgroundRecent advances in targeting the “undruggable” proteins: from drug discovery to clinical trials
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Metadata
- Authors
- He, M., Cao, C., Ni, Z., Liu, Y., Song, P., Hao, S., He, Y., Sun, X., & Rao, Y.
- Affiliations
- Tsinghua University (CN)
- Zhengzhou University (CN)
- Corresponding author
- Rao, Yu
- Venue
- Signal Transduction and Targeted Therapy
- Published
- 2022-06-09
- Volume
- 7
- Issue
- 1
- Pages
- 181-181
- ISSN
- 2059-3635 (ISSN-L)
- PMC
- PMC9178337
- OpenAlex
- W4281795388
- Cited by
- 283
- References
- 559
- Citations by year
- 2026: 50 · 2025: 82 · 2024: 84 · 2023: 50 · 2022: 17
- FWCI
- 6.14
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Signal Transduction and Targeted Therapy (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Funders
- National Natural Science Foundation of China (#82125034, #81773567, 2021YFA1302100, 2020YFE0202200)
- China Postdoctoral Science Foundation
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Degradation and Inhibitors
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
- Physical Sciences › Chemistry › Organic Chemistry › Chemical Synthesis and Analysis
- Keywords
- PROTACs, protein degradation, bifunctional small molecules, ubiquitination, ubiquitin-proteasome system, molecular glues, small-molecule degraders, clinical development, cancer therapy
- MeSH terms
- Ubiquitin-Protein Ligases, Proteasome Endopeptidase Complex, Proteolysis
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