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CRBN-PROTACs in Cancer Therapy: From Mechanistic Insights to Clinical Applications.
- Source :
-
Chemical biology & drug design [Chem Biol Drug Des] 2024 Nov; Vol. 104 (5), pp. e70009. - Publication Year :
- 2024
-
Abstract
- Cereblon (CRBN), a member of the E3 ubiquitin ligase complex, has gained significant attention as a therapeutic target in cancer. CRBN regulates the degradation of various proteins in cancer progression, including transcription factors and signaling molecules. PROTACs (proteolysis-targeting chimeras) are a novel approach that uses the cell's degradation system to remove disease-causing proteins selectively. CRBN-dependent PROTACs work by tagging harmful proteins for destruction through the ubiquitin-proteasome system. This strategy offers several advantages over traditional protein inhibition methods, including the potential to overcome drug resistance. Recent progress in developing CRBN-based PROTACs has shown promising preclinical results in both hematologic malignancies and solid tumors. Additionally, CRBN-based PROTACs have enhanced our understanding of CRBN's role in cancer, potentially serving as biomarkers for patient stratification and predicting therapeutic responses. In this review, we delineate the mechanisms of action for CRBN-dependent PROTACs (CRBN-PROTACs), summarize recent advances in preclinical and clinical applications, and provide our perspective on future development.<br /> (© 2024 John Wiley & Sons Ltd.)
- Subjects :
- Humans
Adaptor Proteins, Signal Transducing metabolism
Adaptor Proteins, Signal Transducing antagonists & inhibitors
Antineoplastic Agents pharmacology
Antineoplastic Agents chemistry
Antineoplastic Agents therapeutic use
Animals
Proteasome Endopeptidase Complex metabolism
Proteolysis Targeting Chimera
Neoplasms drug therapy
Neoplasms metabolism
Neoplasms pathology
Ubiquitin-Protein Ligases metabolism
Ubiquitin-Protein Ligases antagonists & inhibitors
Proteolysis drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1747-0285
- Volume :
- 104
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Chemical biology & drug design
- Publication Type :
- Academic Journal
- Accession number :
- 39496477
- Full Text :
- https://doi.org/10.1111/cbdd.70009