Evidence map›Paper›PMID 30649890›Full record

ArticleAmerican journal of physiology. Renal physiology2019

Inhibition of 5-lipoxygenase decreases renal fibrosis and progression of chronic kidney disease.

John R Montford, Colin Bauer, Evgenia Dobrinskikh, Katharina Hopp, Moshe Levi, Mary Weiser-Evans, Raphael Nemenoff, Seth B Furgeson

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 24% 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

13 citing papers in PubMed, 25 citations in OpenAlex.

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  11. Review
  12. Therapeutic Implications of Ferroptosis in Renal Fibrosis.Frontiers in molecular biosciences · 2022
    Review
  13. The role of 5-lipoxygenase in the pathophysiology of COVID-19 and its therapeutic implications.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2021
    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

8 authors at 2 institutions in 1 country.

John R MontfordDivision of Renal Diseases and Hypertension, University of Colorado-Anschutz Medical Campus , Denver, Colorado.
Colin BauerDivision of Renal Diseases and Hypertension, University of Colorado-Anschutz Medical Campus , Denver, Colorado.
Evgenia DobrinskikhDepartment of Medicine, University of Colorado-Anschutz Medical Campus , Denver, Colorado.
Katharina HoppDivision of Renal Diseases and Hypertension, University of Colorado-Anschutz Medical Campus , Denver, Colorado.
Moshe LeviDepartment of Biochemistry and Molecular and Cellular Biology, Georgetown University , Washington, District of Columbia.
Mary Weiser-EvansDivision of Renal Diseases and Hypertension, University of Colorado-Anschutz Medical Campus , Denver, Colorado.
Raphael NemenoffDivision of Renal Diseases and Hypertension, University of Colorado-Anschutz Medical Campus , Denver, Colorado.
Seth B FurgesonDivision of Renal Diseases and Hypertension, University of Colorado-Anschutz Medical Campus , Denver, Colorado.
University of Colorado Anschutz Medical Campus · USGeorgetown University · US

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
Colorado Clinical and Translational Sciences InstituteUL1TR001082 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$48.0M
ZEBRAFISH TRANSGENIC CORE - ROCKY MOUNTAIN NEUROLOGICAL DISORDERS CORE CENTERP30NS048154 · NINDS · UNIVERSITY OF COLORADO DENVER · PI RIBERA, ANGELES BADELL · 2004 to 2020
$10.1M
The Role of Bone Marrow Derived Eicosanoids in Renal Disease ProgressionIK2BX003839 · VA · VA EASTERN COLORADO HEALTH CARE SYSTEM · PI MONTFORD, JOHN ROSS · 2018 to 2024
–
BLRD VA IK2 BX003839NCATS NIH HHS UL1 TR001082NCI NIH HHS P30 CA046934NINDS NIH HHS P30 NS048154
6 · The paper itself

Abstract

In inflammatory diseases, the 5-lipoxygenase (5-LO) pathway contributes to epithelial damage and fibrosis by catalyzing the production of leukotrienes (LTs). Antagonists of the 5-LO pathway are currently approved for use in patients and are well tolerated. We found that expression of 5-LO is strongly induced in three models of chronic kidney disease: unilateral ureteral obstruction (UUO), folate nephropathy, and an orthologous mouse model of polycystic kidney disease. Immunohistochemistry showed that macrophages are the dominant source of 5-LO. Zileuton, a US Food and Drug Administration-approved antagonist of 5-LO, significantly reduced fibrosis at 7 and 14 days after UUO; these findings were confirmed using a genetically modified [5-LO-associated protein-knockout ( Alox5ap

Indexed as

AnimalsArachidonate 5-LipoxygenaseFibrosisKidneyKidney TubulesLipoxygenase InhibitorsMice, Inbred C57BLMice, KnockoutPolycystic Kidney DiseasesReceptors, LeukotrieneRenal Insufficiency, ChronicSignal TransductionUreteral ObstructionArachidonate 5-Lipoxygenaseleukotriene C4 receptorLipoxygenase InhibitorsReceptors, Leukotriene5-lipoxygenasefibrosisfluorescence-lifetime imaging microscopykidneyleukotrienes

Identifiers

PMID30649890
PMCPMC6483031
OpenAlexW2910616615

What OpenQuestion holds

Textmetadata
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.