Fibronectin-targeted FUD and PEGylated FUD peptides for fibrotic diseases.


Journal

Journal of controlled release : official journal of the Controlled Release Society
ISSN: 1873-4995
Titre abrégé: J Control Release
Pays: Netherlands
ID NLM: 8607908

Informations de publication

Date de publication:
08 2023
Historique:
received: 25 02 2023
revised: 03 06 2023
accepted: 06 06 2023
pmc-release: 01 08 2024
medline: 21 8 2023
pubmed: 15 6 2023
entrez: 14 6 2023
Statut: ppublish

Résumé

Tissue fibrosis is characterized by excessive deposition of extracellular matrix (ECM) molecules. Fibronectin (FN) is a glycoprotein found in the blood and tissues, a key player in the assembly of ECM through interaction with cellular and extracellular components. Functional Upstream Domain (FUD), a peptide derived from an adhesin protein of bacteria, has a high binding affinity for the N-terminal 70-kDa domain of FN that plays a crucial role in FN polymerization. In this regard, FUD peptide has been characterized as a potent inhibitor of FN matrix assembly, reducing excessive ECM accumulation. Furthermore, PEGylated FUD was developed to prevent rapid elimination of FUD and enhance its systemic exposure in vivo. Herein, we summarize the development of FUD peptide as a potential anti-fibrotic agent and its application in experimental fibrotic diseases. In addition, we discuss how modification of the FUD peptide via PEGylation impacts pharmacokinetic profiles of the FUD peptide and can potentially contribute to anti-fibrosis therapy.

Identifiants

pubmed: 37315694
pii: S0168-3659(23)00378-4
doi: 10.1016/j.jconrel.2023.06.008
pmc: PMC10527082
mid: NIHMS1908484
pii:
doi:

Substances chimiques

Adhesins, Bacterial 0
Fibronectins 0
Peptides 0
Polyethylene Glycols 3WJQ0SDW1A

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

69-81

Subventions

Organisme : NCI NIH HHS
ID : R01 CA257837
Pays : United States
Organisme : NCI NIH HHS
ID : R21 CA252579
Pays : United States

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest None.

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Auteurs

Hye Jin Lee (HJ)

Pharmaceutical Sciences Division, School of Pharmacy, University of Wisconsin - Madison, 777 Highland Avenue, Madison, WI 53705, USA.

Bianca R Tomasini-Johansson (BR)

Department of Cell and Regenerative Biology, School of Medicine and Public Health, University of Wisconsin - Madison, 1111 Highland Avenue, WIMRII, Madison, WI 53705, USA.

Nikesh Gupta (N)

Pharmaceutical Sciences Division, School of Pharmacy, University of Wisconsin - Madison, 777 Highland Avenue, Madison, WI 53705, USA.

Glen S Kwon (GS)

Pharmaceutical Sciences Division, School of Pharmacy, University of Wisconsin - Madison, 777 Highland Avenue, Madison, WI 53705, USA; Carbone Cancer Center, University of Wisconsin - Madison, 600 Highland Avenue, Madison, WI 53705, USA. Electronic address: glen.kwon@wisc.edu.

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Classifications MeSH