Therapeutic and diagnostic targeting of fibrosis in metabolic, proliferative and viral disorders.

Adv Drug Deliv Rev

Department of Nanomedicine and Theranostics, Institute for Experimental Molecular Imaging, Faculty of Medicine, RWTH Aachen University, Aachen, Germany; Department of Pharmaceutics, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Utrecht, the Netherlands; Department of Targeted Therapeutics, University of Twente, Enschede, the Netherlands. Electronic address:

Published: August 2021

AI Article Synopsis

  • * The article explores different anti-fibrotic targets, including cells, genes, and proteins, while highlighting recent advancements in anti-fibrotic therapies and the role of nanomedicine in enhancing treatment effectiveness.
  • * It also covers the use of medical imaging techniques for diagnosing, staging, and monitoring fibrotic disorders, aiming to improve individualized treatment strategies for affected patients.

Article Abstract

Fibrosis is a common denominator in many pathologies and crucially affects disease progression, drug delivery efficiency and therapy outcome. We here summarize therapeutic and diagnostic strategies for fibrosis targeting in atherosclerosis and cardiac disease, cancer, diabetes, liver diseases and viral infections. We address various anti-fibrotic targets, ranging from cells and genes to metabolites and proteins, primarily focusing on fibrosis-promoting features that are conserved among the different diseases. We discuss how anti-fibrotic therapies have progressed over the years, and how nanomedicine formulations can potentiate anti-fibrotic treatment efficacy. From a diagnostic point of view, we discuss how medical imaging can be employed to facilitate the diagnosis, staging and treatment monitoring of fibrotic disorders. Altogether, this comprehensive overview serves as a basis for developing individualized and improved treatment strategies for patients suffering from fibrosis-associated pathologies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7611899PMC
http://dx.doi.org/10.1016/j.addr.2021.113831DOI Listing

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