Evidence map›Paper›PMID 34235177›Full record

ArticleFrontiers in molecular biosciences2021

GSK-3 Inhibition Modulates Metalloproteases in a Model of Lung Inflammation and Fibrosis.

Francesco Cinetto, Jessica Ceccato, Ilaria Caputo, Daniela Cangiano, Barbara Montini, Francesca Lunardi, Maria Piazza, Carlo Agostini, Fiorella Calabrese, Gianpietro Semenzato and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in molecular biosciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
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  4. Article
  5. Article
  6. Immune Mechanisms of Pulmonary Fibrosis with Bleomycin.International journal of molecular sciences · 2023
    Review
  7. Article
  8. Article
  9. 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

15 authors at 3 institutions in 1 country.

Francesco CinettoInternal Medicine and Allergology and Clinical Immunology Units, Treviso Ca' Foncello Hospital, Treviso, Italy.
Jessica CeccatoHematology Unit, Department of Medicine, University of Padova, Padova, Italy.
Ilaria CaputoHematology Unit, Department of Medicine, University of Padova, Padova, Italy.
Daniela CangianoHematology Unit, Department of Medicine, University of Padova, Padova, Italy.
Barbara MontiniInstitute of Pediatric Research (IRP) Città Della Speranza, Padua, Italy.
Francesca LunardiDepartment of Cardiothoracic and Vascular Sciences, Pathology Section, University of Padova, Padua, Italy.
Maria PiazzaHematology Unit, Department of Medicine, University of Padova, Padova, Italy.
Carlo AgostiniInternal Medicine and Allergology and Clinical Immunology Units, Treviso Ca' Foncello Hospital, Treviso, Italy.
Fiorella CalabreseDepartment of Cardiothoracic and Vascular Sciences, Pathology Section, University of Padova, Padua, Italy.
Gianpietro SemenzatoHematology Unit, Department of Medicine, University of Padova, Padova, Italy.
Marcello RattazziInternal Medicine and Allergology and Clinical Immunology Units, Treviso Ca' Foncello Hospital, Treviso, Italy.
Carmela GurrieriHematology Unit, Department of Medicine, University of Padova, Padova, Italy.
Riccardo ScarpaInternal Medicine and Allergology and Clinical Immunology Units, Treviso Ca' Foncello Hospital, Treviso, Italy.
Carla FeliceHematology Unit, Department of Medicine, University of Padova, Padova, Italy.
Fabrizio VianelloHematology Unit, Department of Medicine, University of Padova, Padova, Italy.
University of Padua · ITCa' Foncello Hospital · ITCittà della Speranza Foundation · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Idiopathic pulmonary fibrosis (IPF) is mainly characterized by aberrant extracellular matrix deposition, consequent to epithelial lung injury and myofibroblast activation, and inflammatory response. Glycogen synthase kinase 3 (GSK-3) is a serine-threonine kinase involved in several pathways, and its inhibition has been already suggested as a therapeutic strategy for IPF patients. There is evidence that GSK-3 is able to induce matrix metalloproteinase (MMP) expression and that its inhibition modulates MMP expression in the tissues. The aim of our study was to investigate the role of GSK-3 and its inhibition in the modulation of MMP-9 and -2 in an

Indexed as

bleomycin-induced lung injuryextracellular matrix (ECM)glycogen synthase kinase 3idiopathic lung fibrosismetalloproteases

Identifiers

PMID34235177
PMCPMC8255387
OpenAlexW3177150124

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.