Evidence map›Paper›PMID 36309093›Full record

ArticleThe Journal of biological chemistry2022

Salt-inducible kinase 2 regulates fibrosis during bleomycin-induced lung injury.

Manuel van Gijsel-Bonnello, Nicola J Darling, Takashi Tanaka, Samuele Di Carmine, Francesco Marchesi, Sarah Thomson, Kristopher Clark, Mariola Kurowska-Stolarska, Henry J McSorley, Philip Cohen and 1 more

Open access · goldAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2022. 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
1.4field-weighted citation impact, top 18% 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
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  4. Review
  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

11 authors at 3 institutions in 2 countries.

Manuel van Gijsel-BonnelloDivision of Cell Signalling and Immunology, School of Life Sciences, University of Dundee, Dundee, United Kingdom; MRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dundee, United Kingdom.
Nicola J DarlingMRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dundee, United Kingdom.
Takashi TanakaResearch Centre of Specialty, Ono Pharmaceutical Co Ltd, Osaka, Japan.
Samuele Di CarmineDivision of Cell Signalling and Immunology, School of Life Sciences, University of Dundee, Dundee, United Kingdom.
Francesco MarchesiSchool of Veterinary Medicine, College of Medical Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom.
Sarah ThomsonBiological Services, University of Dundee, Dundee, United Kingdom.
Kristopher ClarkMRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dundee, United Kingdom.
Mariola Kurowska-StolarskaInstitute of Infection, Immunity and Inflammation, College of Medical Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom.
Henry J McSorleyDivision of Cell Signalling and Immunology, School of Life Sciences, University of Dundee, Dundee, United Kingdom.
Philip CohenMRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dundee, United Kingdom.
J Simon C ArthurDivision of Cell Signalling and Immunology, School of Life Sciences, University of Dundee, Dundee, United Kingdom. Electronic address: j.s.c.arthur@dundee.ac.uk.
University of Dundee · GBUniversity of Glasgow · GBOno Pharmaceutical (Japan) · JP

Funding

Medical Research Council MR/R021406/1Medical Research Council MR/V036998/1Versus Arthritis 20623Versus Arthritis 21425Versus Arthritis 22272
6 · The paper itself

Abstract

Idiopathic pulmonary fibrosis is a progressive and normally fatal disease with limited treatment options. The tyrosine kinase inhibitor nintedanib has recently been approved for the treatment of idiopathic pulmonary fibrosis, and its effectiveness has been linked to its ability to inhibit a number of receptor tyrosine kinases including the platelet-derived growth factor, vascular endothelial growth factor, and fibroblast growth factor receptors. We show here that nintedanib also inhibits salt-inducible kinase 2 (SIK2), with a similar IC

Indexed as

Idiopathic Pulmonary FibrosisLung InjuryAnimalsBleomycinDisease Models, AnimalFibrosisLungMiceProtein Serine-Threonine KinasesVascular Endothelial Growth Factor ABleomycinProtein Serine-Threonine KinasesSIK3 protein, mouseVascular Endothelial Growth Factor Akinase inhibitornintedanibpulmonary fibrosisSIK1SIK2SIK3

Identifiers

PMID36309093
PMCPMC9706632
OpenAlexW4307658948

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.