Evidence map›Paper›PMID 32697651›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2020

Neonatal therapy with PF543, a sphingosine kinase 1 inhibitor, ameliorates hyperoxia-induced airway remodeling in a murine model of bronchopulmonary dysplasia.

Alison W Ha, Tara Sudhadevi, David L Ebenezer, Panfeng Fu, Evgeny V Berdyshev, Steven J Ackerman, Viswanathan Natarajan, Anantha Harijith

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.4field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Targeting sphingosine kinase 1 in p53KO thymic lymphoma.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Article
  7. Review
  8. Review
  9. Review
  10. Sphingolipids in mitochondria-from function to disease.Frontiers in cell and developmental biology · 2023
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Hyperoxia-induced S1PCell biochemistry and biophysics · 2021
    Article
  16. My Journey in Academia as a Lipid Biochemist.Cell biochemistry and biophysics · 2021
    Review
  17. New Pharmacologic Approaches to Bronchopulmonary Dysplasia.Journal of experimental pharmacology · 2021
    Review
  18. Review
  19. Article
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 3 institutions in 1 country.

Alison W HaDepartment of Biochemistry, University of Illinois, Chicago, Illinois.
Tara SudhadeviDepartment of Pediatrics, Case Western Reserve University, Cleveland, Ohio.
David L EbenezerDepartment of Pharmacology, University of Illinois, Chicago, Illinois.
Panfeng FuDepartment of Pharmacology, University of Illinois, Chicago, Illinois.
Evgeny V BerdyshevDepartment of Medicine, National Jewish Health, Denver, Colorado.ORCID 0000-0002-1376-0098
Steven J AckermanDepartment of Biochemistry, University of Illinois, Chicago, Illinois.
Viswanathan NatarajanDepartment of Pharmacology, University of Illinois, Chicago, Illinois.
Anantha HarijithDepartment of Pediatrics, Case Western Reserve University, Cleveland, Ohio.
University of Illinois Chicago · USCase Western Reserve University · USNational Jewish Health · US

Funding

Role of novel SphK1 inhibitor, PF543 in therapy of Bronchopulmonary dysplasia and Airway remodelingR01HD090887 · NICHD · UNIVERSITY OF ILLINOIS AT CHICAGO · PI HARIJITH, ANANTHA · 2018 to 2022
$1.5M
HHS | NIH | National Institute of Child Health and Human Development (NICHD) R01HD090887-01A1NICHD NIH HHS R01 HD090887
6 · The paper itself

Abstract

Hyperoxia (HO)-induced lung injury contributes to bronchopulmonary dysplasia (BPD) in preterm newborns. Intractable wheezing seen in BPD survivors is associated with airway remodeling (AWRM). Sphingosine kinase 1 (SPHK1)/sphingosine-1-phosphate (S1P) signaling promotes HO-mediated neonatal BPD; however, its role in the sequela of AWRM is not known. We noted an increased concentration of S1P in tracheal aspirates of neonatal infants with severe BPD, and earlier, demonstrated that

Indexed as

Airway RemodelingAnimalsAnimals, NewbornBronchopulmonary DysplasiaDisease Models, AnimalHyperoxiaLungMethanolMice, KnockoutPhosphotransferases (Alcohol Group Acceptor)PyrrolidinesReactive Oxygen SpeciesSignal TransductionSphingosine KinaseSulfonesMethanolPF-543Phosphotransferases (Alcohol Group Acceptor)PyrrolidinesReactive Oxygen SpeciesSphingosine KinaseSphk1 protein, mouseSulfonesairway remodelingbronchopulmonary dysplasiamitochondrial ROSPF543sphingosine kinase 1

Identifiers

PMID32697651
PMCPMC7518054
OpenAlexW3043992017

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.