Development of MDM2‐Targeting PROTAC for Advancing Bone Regeneration

Proteolysis-targeting chimeras (PROTACs) degrade target proteins through the ubiquitin-proteasome system. To date, PROTACs are primarily used to treat various diseases; however, they have not been applied in regenerative therapy. Herein, this work introduces MDM2-targeting PROTACs customized for application in bone regeneration. An MDM2-PROTAC library is constructed by combining Nutlin-3 and CRBN ligands with various linker designs. Through a multistep validation process, this work develops MDM2-PROTACs (CL144 and CL174) that presented potent degradation efficiency and a robust inductive effect on the biomineralization. Next, this work performs whole-transcriptome analysis to dissect the biological effects of the CL144, and reveals the upregulation of osteogenic marker genes. Furthermore, CL144 effectively induced bone regeneration in bone graft and ovariectomy (OVX) models after local and systemic administration, respectively. In the OVX model, the combination treatment with CL144 and alendronate induced a synergistic effect. Overall, this study demonstrates the promising role of MDM2-PROTAC in promoting bone regeneration, marking the first step toward expanding the application of the PROTAC technology.

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Publication Details

Journal
Advanced Science
Published
2025-03-24
DOI
https://doi.org/10.1002/advs.202415626
Citations
6
Primary Topic
Protein Degradation and Inhibitors
Type
article
Field-Weighted Citation Impact
4.84

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article

Development of MDM2‐Targeting PROTAC for Advancing Bone Regeneration

Junwon Choi, Sunjoo Choi, Hyun‐Ju An, Tae Hyeon Yoo et al.
6 citations
Advanced Science
Protein Degradation and Inhibitors
4.84
article

Development of MDM2‐Targeting PROTAC for Advancing Bone Regeneration

Junwon Choi, Sunjoo Choi, Hyun‐Ju An, Tae Hyeon Yoo, Ji‐Min Choi, Jung-Taek Kim, Won-Seok Choi, Jae‐Kook Cha, Minsup Kim, Sun‐Young Kim, Jun‐Seok Lee, Jin Man Kim, Jae Min Lee, Susun An, Seongkeun Jeong, Soonchul Lee, Kyung Tae Hong, Wasim Ahmed
article en
6 citations

Abstract

Proteolysis-targeting chimeras (PROTACs) degrade target proteins through the ubiquitin-proteasome system. To date, PROTACs are primarily used to treat various diseases; however, they have not been applied in regenerative therapy. Herein, this work introduces MDM2-targeting PROTACs customized for application in bone regeneration. An MDM2-PROTAC library is constructed by combining Nutlin-3 and CRBN ligands with various linker designs. Through a multistep validation process, this work develops MDM2-PROTACs (CL144 and CL174) that presented potent degradation efficiency and a robust inductive effect on the biomineralization. Next, this work performs whole-transcriptome analysis to dissect the biological effects of the CL144, and reveals the upregulation of osteogenic marker genes. Furthermore, CL144 effectively induced bone regeneration in bone graft and ovariectomy (OVX) models after local and systemic administration, respectively. In the OVX model, the combination treatment with CL144 and alendronate induced a synergistic effect. Overall, this study demonstrates the promising role of MDM2-PROTAC in promoting bone regeneration, marking the first step toward expanding the application of the PROTAC technology.

Advanced ScienceVol. 12(19)
Harvard University (US), Seoul National University (KR), Yonsei University (KR), Korea University (KR), CHA University Bundang Medical Center (KR), CHA University (KR), Seoul National University Dental Hospital (KR), Ajou University (KR)
Ajou University
Openalex Percentile: Top 5%
Protein Degradation and Inhibitors
4.84
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