MMP-2-triggered, mitochondria-targeted PROTAC-PDT therapy of breast cancer and brain metastases inhibition
Proteolytic targeting chimera (PROTAC) technology is a protein-blocking technique and induces antitumor effects, with potential advantages. However, its effect is limited by insufficient distribution and accumulation in tumors. Herein, a transformable nanomedicine (dBET6@CFMPD) with mitochondrial targeting capacity is designed and constructed to combine PROTAC with photodynamic therapy (PDT). In this work, we demonstrate that dBET6@CFMPD exhibits great biodistribution and retention, and can induce potent antitumor response to suppress primary and metastatic tumors, becoming a nanomedicine with potential in cancer combination therapy.
Authors
- Tao Gong (ORCID: https://orcid.org/0000-0002-9866-9911)
- Yanyan Xu
- Fan Tong (ORCID: https://orcid.org/0000-0002-4333-0128)
- Yujun Song (ORCID: https://orcid.org/0000-0003-2474-084X)
- Yufan Du
- Huile Gao (ORCID: https://orcid.org/0000-0002-5355-7238)
- Ting Lei (ORCID: https://orcid.org/0000-0002-0100-9424)
- Wenqin Yang (ORCID: https://orcid.org/0000-0001-9416-9920)
- Yang Zhou (ORCID: https://orcid.org/0000-0001-6330-7032)
- Yufan Wang
- Siqin He
Institutions
- Hainan University (CN)
- Sichuan University (CN)
- Hainan Medical University (CN)
Publication Details
- Journal
- Nature Communications
- Published
- 2024-11-29
- DOI
- https://doi.org/10.1038/s41467-024-54854-2
- Citations
- 50
- Primary Topic
- Protein Degradation and Inhibitors
- Type
- article
- Field-Weighted Citation Impact
- 11.69
Funders
- National Natural Science Foundation of China