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Targeting endothelial permeability in the EPR effect.

Authors :
Lahooti B
Akwii RG
Zahra FT
Sajib MS
Lamprou M
Alobaida A
Lionakis MS
Mattheolabakis G
Mikelis CM
Source :
Journal of controlled release : official journal of the Controlled Release Society [J Control Release] 2023 Sep; Vol. 361, pp. 212-235. Date of Electronic Publication: 2023 Aug 08.
Publication Year :
2023

Abstract

The characteristics of the primary tumor blood vessels and the tumor microenvironment drive the enhanced permeability and retention (EPR) effect, which confers an advantage towards enhanced delivery of anti-cancer nanomedicine and has shown beneficial effects in preclinical models. Increased vascular permeability is a landmark feature of the tumor vessels and an important driver of the EPR. The main focus of this review is the endothelial regulation of vascular permeability. We discuss current challenges of targeting vascular permeability towards clinical translation and summarize the structural components and mechanisms of endothelial permeability, the principal mediators and signaling players, the targeted approaches that have been used and their outcomes to date. We also critically discuss the effects of the tumor-infiltrating immune cells, their interplay with the tumor vessels and the impact of immune responses on nanomedicine delivery, the impact of anti-angiogenic and tumor-stroma targeting approaches, and desirable nanoparticle design approaches for greater translational benefit.<br />Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2023. Published by Elsevier B.V.)

Details

Language :
English
ISSN :
1873-4995
Volume :
361
Database :
MEDLINE
Journal :
Journal of controlled release : official journal of the Controlled Release Society
Publication Type :
Academic Journal
Accession number :
37517543
Full Text :
https://doi.org/10.1016/j.jconrel.2023.07.039