Skip to content
2000
Volume 9, Issue 2
  • ISSN: 1573-4080
  • E-ISSN: 1875-6662

Abstract

When extensive, fibrosis can impair the function of an affected organ. Despite a greater understanding of the causes and processes leading to organ fibrosis, there are a limited number of treatment options with minimal data supporting their utility. Identifying compounds for clinical use that inhibit fibrosis is an active area of investigation. In recent years, evidence for the utility of targeting the ubiquitin-proteasome system (UPS) in the inhibition of fibrosis has grown. Here we review the evidence for the interaction of the UPS with processes driving organ fibrosis, including the transforming growth factor beta pathway. We will also discuss the potential utility and harm of proteasome inhibition in the treatment of organ fibrosis.

Loading

Article metrics loading...

/content/journals/cei/10.2174/1573408011309020008
2013-09-01
2025-11-05
Loading full text...

Full text loading...

/content/journals/cei/10.2174/1573408011309020008
Loading

  • Article Type:
    Research Article
Keyword(s): Bortezomib; fibrosis; proteasome; transforming growth factor-beta; ubiquitin
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test