Evidence map›Paper›PMID 30343604›Full record

ReviewConnective tissue research2019

Fine-tuning the ubiquitin-proteasome system to treat pulmonary fibrosis.

Willy Roque, Ross Summer, Freddy Romero

Abstract readReview
In one paragraph

Review in Connective tissue research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.5field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 14 citations in OpenAlex.

  1. The AhR Is a Critical Regulator of the Pulmonary Response to Cannabis Smoke.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  2. Article
  3. Bortezomib Inhibits Lung Fibrosis and Fibroblast Activation without Proteasome Inhibition.American journal of respiratory cell and molecular biology · 2022
    Article
  4. Article
  5. The Ubiquitin Proteasome System and Skin Fibrosis.Molecular diagnosis & therapy · 2021
    Review
  6. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Willy Roquea Center for Translational Medicine and Jane and Leonard Korman Lung Center , Thomas Jefferson University , Philadelphia , PA , USA.
Ross Summera Center for Translational Medicine and Jane and Leonard Korman Lung Center , Thomas Jefferson University , Philadelphia , PA , USA.
Freddy Romeroa Center for Translational Medicine and Jane and Leonard Korman Lung Center , Thomas Jefferson University , Philadelphia , PA , USA.
Thomas Jefferson University · US

Funding

Metabolic control of DNA repair in pulmonary fibrosisR01HL131784 · NHLBI · THOMAS JEFFERSON UNIVERSITY · PI SUMMER, ROSS S · 2017 to 2020
$1.6M
PROTEASOME DEGRADATION OF P53 DRIVES HPS LUNG FIBROSISR01HL136833 · NHLBI · THOMAS JEFFERSON UNIVERSITY · PI ROMERO, FREDDY · 2018 to 2021
$1.6M
NHLBI NIH HHS R01 HL131784NHLBI NIH HHS R01 HL136833
6 · The paper itself

Abstract

Idiopathic pulmonary fibrosis (IPF) is an extremely aggressive lung disease that develops almost exclusively in older individuals, carries a very poor prognosis, and lacks any truly effective therapies. The current conceptual model is that IPF develops because of an age-related decline in the ability of the lung epithelium to regenerate after injury, largely due to death or senescence of epithelial progenitor cells in the distal airways. This loss of regenerative capacity is thought to initiate a chronic and ineffective wound-healing response, characterized by persistent, low-grade lung inflammation and sustained production of collagen and other extracellular matrix materials. Despite recent advances in our understanding of IPF pathobiology, there remains a pressing need to further delineate underlying mechanisms to develop more effective therapies for this disease. In this review, we build the case that many of the manifestations of IPF result from a failure of cells to effectively manage their proteome. We propose that epithelial progenitor cells, as well as immune cells and fibroblasts, become functionally impaired, at least in part, because of an accumulation or a loss in the expression of various crucial proteins. Further, we propose that central to this defect is the dysregulation of the ubiquitin-proteasome system (UPS), which is the major protein-degradation system in eukaryotic cells. Lastly, borrowing concepts from other fields, we discuss how targeting the UPS system could be employed as a novel treatment for IPF and perhaps for other fibrotic lung diseases as well.

Indexed as

HumansIdiopathic Pulmonary FibrosisMitochondriaMolecular Targeted TherapyProteasome Endopeptidase ComplexProteomeUbiquitinProteasome Endopeptidase ComplexProteomeUbiquitinIdiopathic pulmonary fibrosisproteostasisPulmonary fibrosisubiquitin-proteasome system

Identifiers

PMID30343604
PMCPMC6373466
OpenAlexW2898184693

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.