Progress on the Application of Bortezomib and Bortezomib-Based Nanoformulations
Overview
Molecular Biology
Affiliations
Bortezomib (BTZ) is the first proteasome inhibitor approved by the Food and Drug Administration. It can bind to the amino acid residues of the 26S proteasome, thereby causing the death of tumor cells. BTZ plays an irreplaceable role in the treatment of mantle cell lymphoma and multiple myeloma. Moreover, its use in the treatment of other hematological cancers and solid tumors has been investigated in numerous clinical trials and preclinical studies. Nevertheless, the applications of BTZ are limited due to its insufficient specificity, poor permeability, and low bioavailability. Therefore, in recent years, different BTZ-based drug delivery systems have been evaluated. In this review, we firstly discussed the functions of proteasome inhibitors and their mechanisms of action. Secondly, the properties of BTZ, as well as recent advances in both clinical and preclinical research, were reviewed. Finally, progress in research regarding BTZ-based nanoformulations was summarized.
The potential link between the development of Alzheimer's disease and osteoporosis.
Nasme F, Behera J, Tyagi P, Debnath N, Falcone J, Tyagi N Biogerontology. 2025; 26(1):43.
PMID: 39832071 DOI: 10.1007/s10522-024-10181-z.
Pharmaceutical Agents for Targeting Autophagy and Their Applications in Clinics.
Kench U, Sologova S, Smolyarchuk E, Prassolov V, Spirin P Pharmaceuticals (Basel). 2024; 17(10).
PMID: 39458996 PMC: 11510022. DOI: 10.3390/ph17101355.
Anti-tumor effect of proteasome inhibitor on canine urothelial carcinoma.
Kodera Y, Iguchi T, Kato D, Ikeda N, Shinada M, Aoki S J Vet Med Sci. 2024; 86(9):961-965.
PMID: 39034152 PMC: 11422692. DOI: 10.1292/jvms.23-0094.
Actinomycin D and bortezomib disrupt protein homeostasis in Wilms tumor.
Tiburcio P, Chen K, Xu L, Chen K bioRxiv. 2024; .
PMID: 38948702 PMC: 11212905. DOI: 10.1101/2024.06.11.598518.
Anti-BCMA-engineered exosomes for bortezomib-targeted delivery in multiple myeloma.
Yuan S, Li Q, He C, Bing M, Zhang X, Xu H Blood Adv. 2024; 8(18):4886-4899.
PMID: 38875465 PMC: 11421322. DOI: 10.1182/bloodadvances.2023012464.