Evidence map›Paper›PMID 32169655›Full record

ReviewBiochimica et biophysica acta. Molecular and cell biology of lipids2020

Advancements in understanding the role of lysophospholipids and their receptors in lung disorders including bronchopulmonary dysplasia.

Tara Sudhadevi, Alison W Ha, David L Ebenezer, Panfeng Fu, Vijay Putherickal, Viswanathan Natarajan, Anantha Harijith

Open access · greenAbstract readReview
In one paragraph

Review in Biochimica et biophysica acta. Molecular and cell biology of lipids, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Hyperoxia-induced S1PCell biochemistry and biophysics · 2021
    Article
  4. Article
  5. 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

7 authors at 1 institution in 1 country.

Tara SudhadeviDepartment of Pediatrics, University of Illinois, Chicago, IL, United States of America.
Alison W HaDepartment of Biochemistry and Molecular Genetics, University of Illinois, Chicago, IL, United States of America.
David L EbenezerDepartment of Biochemistry and Molecular Genetics, University of Illinois, Chicago, IL, United States of America.
Panfeng FuDepartment of Pharmacology, University of Illinois, Chicago, IL, United States of America.
Vijay PutherickalDepartment of Pharmacology, University of Illinois, Chicago, IL, United States of America.
Viswanathan NatarajanDepartment of Pharmacology, University of Illinois, Chicago, IL, United States of America; Department of Medicine, University of Illinois, Chicago, IL, United States of America.
Anantha HarijithDepartment of Pediatrics, University of Illinois, Chicago, IL, United States of America; Department of Biochemistry and Molecular Genetics, University of Illinois, Chicago, IL, United States of America; Department of Pharmacology, University of Illinois, Chicago, IL, United States of America. Electronic address: harijith@uic.edu.
University of Illinois Chicago · US

Funding

Structure-Function Analysis of nmMLCK in EC Barrier ResponsesP01HL126609 · NHLBI · UNIVERSITY OF FLORIDA · PI Joe G. N. Garcia · 2016 to 2026
$24.4M
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
NHLBI NIH HHS P01 HL126609NICHD NIH HHS R01 HD090887
6 · The paper itself

Abstract

Bronchopulmonary dysplasia (BPD) is a devastating chronic neonatal lung disease leading to serious adverse consequences. Nearly 15 million babies are born preterm accounting for >1 in 10 births globally. The aetiology of BPD is multifactorial and the survivors suffer lifelong respiratory morbidity. Lysophospholipids (LPL), which include sphingosine-1-phosphate (S1P), and lysophosphatidic acid (LPA) are both naturally occurring bioactive lipids involved in a variety of physiological and pathological processes such as cell survival, death, proliferation, migration, immune responses and vascular development. Altered LPL levels have been observed in a number of lung diseases including BPD, which underscores the importance of these signalling lipids under normal and pathophysiological situations. Due to the paucity of information related to LPLs in BPD, most of the ideas related to BPD and LPL are speculative. This article is intended to promote discussion and generate hypotheses, in addition to the limited review of information related to BPD already established in the literature.

Indexed as

AnimalsBronchopulmonary DysplasiaHumansLysophospholipidsReceptors, LysosphingolipidLysophospholipidsReceptors, LysosphingolipidBronchopulmonary dysplasiaG-protein coupled receptorsLysophosphatidic acidLysophospholipidsSignal transductionSphingosine-1-phosphate

Identifiers

PMID32169655
PMCPMC7206974
OpenAlexW3011826193

What Socratic 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 Socratic graph.