Evidence map›Paper›PMID 26938939›Full record

ReviewRedox biology2016

Lung extracellular matrix and redox regulation.

Walter H Watson, Jeffrey D Ritzenthaler, Jesse Roman

Open access · goldAbstract readReview
In one paragraph

Review in Redox biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
6.9field-weighted citation impact, top 3% 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

41 citing papers in PubMed, 71 citations in OpenAlex.

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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 2 institutions in 1 country.

Walter H WatsonDepartment of Medicine, Divisions of Pulmonary, Critical Care and Sleep Disorders and Gastroenterology, Hepatology and Nutrition, University of Louisville, Health Sciences Center, Louisville, KY, United States; Department of Pharmacology & Toxicology, University of Louisville, Health Sciences Center, Louisville, KY, United States.
Jeffrey D RitzenthalerDepartment of Medicine, Divisions of Pulmonary, Critical Care and Sleep Disorders and Gastroenterology, Hepatology and Nutrition, University of Louisville, Health Sciences Center, Louisville, KY, United States.
Jesse RomanDepartment of Medicine, Divisions of Pulmonary, Critical Care and Sleep Disorders and Gastroenterology, Hepatology and Nutrition, University of Louisville, Health Sciences Center, Louisville, KY, United States; Department of Pharmacology & Toxicology, University of Louisville, Health Sciences Center, Louisville, KY, United States; Robley Rex Veterans Affairs Medical Center, Louisville, KY, United States. Electronic address: j.roman@louisville.edu.
University of Louisville · USLouisville VA Medical Center · US

Funding

The Impact of Oxidative Stress on HIV-induced Lung DiseaseU01HL121807 · NHLBI · UNIVERSITY OF LOUISVILLE · PI RAMIREZ, JULIO ALBERTO, ROMAN, JESSE · 2013 to 2017
$2.7M
Receptor-mediated effects of ethanol in lung tissue injury and repairR01AA019953 · NIAAA · UNIVERSITY OF LOUISVILLE · PI ROMAN, JESSE · 2012 to 2016
$1.6M
Nicotine-induced fibronectin expression in lung injury and repairI01BX000216 · VA · VETERANS HEALTH ADMINISTRATION · PI ROMAN, JESSE · 2009 to 2018
–
BLRD VA I01 BX000216NHLBI NIH HHS U01 HL121807NIAAA NIH HHS R01 AA019953
6 · The paper itself

Abstract

Pulmonary fibrosis affects millions worldwide and, even though there has been a significant investment in understanding the processes involved in wound healing and maladaptive repair, a complete understanding of the mechanisms responsible for lung fibrogenesis eludes us, and interventions capable of reversing or halting disease progression are not available. Pulmonary fibrosis is characterized by the excessive expression and uncontrolled deposition of extracellular matrix (ECM) proteins resulting in erosion of the tissue structure. Initially considered an 'end-stage' process elicited after injury, these events are now considered pathogenic and are believed to contribute to the course of the disease. By interacting with integrins capable of signal transduction and by influencing tissue mechanics, ECM proteins modulate processes ranging from cell adhesion and migration to differentiation and growth factor expression. In doing so, ECM proteins help orchestrate complex developmental processes and maintain tissue homeostasis. However, poorly controlled deposition of ECM proteins promotes inflammation, fibroproliferation, and aberrant differentiation of cells, and has been implicated in the pathogenesis of pulmonary fibrosis, atherosclerosis and cancer. Considering their vital functions, ECM proteins are the target of investigation, and oxidation-reduction (redox) reactions have emerged as important regulators of the ECM. Oxidative stress invariably accompanies lung disease and promotes ECM expression directly or through the overproduction of pro-fibrotic growth factors, while affecting integrin binding and activation. In vitro and in vivo investigations point to redox reactions as targets for intervention in pulmonary fibrosis and related disorders, but studies in humans have been disappointing probably due to the narrow impact of the interventions tested, and our poor understanding of the factors that regulate these complex reactions. This review is not meant to provide a comprehensive review of this field, but rather to highlight what has been learned and to raise interest in this area in need of much attention.

Indexed as

Cell AdhesionExtracellular MatrixExtracellular Matrix ProteinsHomeostasisHumansLungOxidation-ReductionOxidative StressPulmonary FibrosisSignal TransductionExtracellular Matrix ProteinsExtracellular matrixIntegrinsOxidative stressPulmonary fibrosisRedox

Identifiers

PMID26938939
PMCPMC4777985
OpenAlexW2278097264

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.