Evidence map›Paper›PMID 29283216›Full record

ArticleProteomics. Clinical applications2018

A Lipidomics Approach to Identifying Key Lipid Species Involved in VEGF-Inhibitor Mediated Attenuation of Bleomycin-Induced Pulmonary Fibrosis.

Yogesh M Kulkarni, Sucharita Dutta, Anand Krishnan V Iyer, Clayton A Wright, Vani Ramesh, Vivek Kaushik, Oliver John Semmes, Neelam Azad

Open access · greenAbstract read
In one paragraph

Article in Proteomics. Clinical applications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 30 citations in OpenAlex.

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  9. Efficacy and Safety of Dahuang Zhechong Pill in Silicosis: A Randomized Controlled Trial.Evidence-based complementary and alternative medicine : eCAM · 2021
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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

8 authors at 2 institutions in 1 country.

Yogesh M KulkarniDepartment of Pharmaceutical Sciences, School of Pharmacy, Hampton University, Hampton, VA, USA.
Sucharita DuttaLeroy T. Canoles Jr., Cancer Research Center, Eastern Virginia Medical School, Norfolk, VA,, USA.
Anand Krishnan V IyerDepartment of Pharmaceutical Sciences, School of Pharmacy, Hampton University, Hampton, VA, USA.
Clayton A WrightDepartment of Pharmaceutical Sciences, School of Pharmacy, Hampton University, Hampton, VA, USA.
Vani RameshDepartment of Obstetrics and Gynecology, The Jones Institute for Reproductive Medicine, Eastern Virginia Medical School, Norfolk, VA, USA.
Vivek KaushikDepartment of Pharmaceutical Sciences, School of Pharmacy, Hampton University, Hampton, VA, USA.
Oliver John SemmesLeroy T. Canoles Jr., Cancer Research Center, Eastern Virginia Medical School, Norfolk, VA,, USA.
Neelam AzadDepartment of Pharmaceutical Sciences, School of Pharmacy, Hampton University, Hampton, VA, USA.
Hampton University · USEastern Virginia Medical School · US

Funding

Anti-Tumorigenic Potential of Novel Digitoxin AnaloguesSC1CA173069 · NCI · HAMPTON UNIVERSITY · PI IYER, ANAND K. · 2012 to 2016
$1.3M
Impact of Oxidative Stress-Regulated Angiogenesis in Pulmonary FibrosisSC1HL112630 · NHLBI · HAMPTON UNIVERSITY · PI AZAD, NEELAM · 2011 to 2015
$1.3M
Targeting Lipogenic and Angiogenic Mediators in Pulmonary FibrosisSC1GM121287 · NIGMS · HAMPTON UNIVERSITY · PI AZAD, NEELAM · 2018 to 2021
$1.3M
NCI NIH HHS SC1 CA173069NHLBI NIH HHS SC1 HL112630NIGMS NIH HHS SC1 GM121287
6 · The paper itself

Abstract

purposePoor molecular characterization of idiopathic pulmonary fibrosis (IPF) has led to insufficient understanding of the pathogenesis of the disease, resulting in lack of effective therapies and poor prognosis. Particularly, the role of lipid imbalance due to impaired lipid metabolism in the pathogenesis of IPF has been poorly studied. EXPERIMENTAL

designThe authors have used shotgun lipidomics in a bleomycin (BLM) mouse model of pulmonary fibrosis with vascular endothelial growth factor (VEGF)-inhibitor CBO-P11 as a therapeutic measure, to identify a comprehensive set of lipids that contribute to the pathogenesis of pulmonary fibrosis.

resultsThe authors report that attenuation of BLM-induced fibrotic response with CBO-P11 cotreatment is accompanied by a decrease in total lipid content and specific downregulation of lipids, which are upregulated in response to BLM treatment. CONCLUSION AND CLINICAL RELEVANCE: Dysregulated lipids identified in this study hold the potential of being future biomarkers for IPF.

Indexed as

Computational BiologyLipid MetabolismAnimalsBleomycinEndothelial Growth FactorsFatty AcidsLungMiceMice, Inbred C57BLPeptides, CyclicPhospholipidsPulmonary FibrosisUp-RegulationVascular Endothelial Growth Factor ABleomycincyclo-VEGIEndothelial Growth FactorsFatty AcidsPeptides, CyclicPhospholipidsVascular Endothelial Growth Factor Ableomyciningenuity pathway analysislipidomicspulmonary fibrosisVEGF-inhibitor

Identifiers

PMID29283216
PMCPMC6368219
OpenAlexW2778079802

What OpenQuestion holds

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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.