Evidence map›Paper›PMID 36901840›Full record

ArticleInternational journal of molecular sciences2023

Proteomic Fingerprint of Lung Fibrosis Progression and Response to Therapy in Bleomycin-Induced Mouse Model.

Lucrezia Principi, Erica Ferrini, Roberta Ciccimarra, Lisa Pagani, Clizia Chinello, Paolo Previtali, Andrew Smith, Gino Villetti, Matteo Zoboli, Francesca Ravanetti and 3 more

Full text read
In one paragraph

Article in International journal of molecular sciences, 2023. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. From Epithelium to Therapy: Transitional Cells in Lung Fibrosis.American journal of respiratory cell and molecular biology · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. 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

13 authors.

Lucrezia PrincipiClinical Proteomics and Metabolomics Unit, Department of Medicine and Surgery, University of Milano-Bicocca, 20854 Monza, Italy.ORCID 0000-0002-0391-7995
Erica FerriniDepartment of Veterinary Science, University of Parma, 43122 Parma, Italy.
Roberta CiccimarraDepartment of Veterinary Science, University of Parma, 43122 Parma, Italy.ORCID 0000-0001-9431-143X
Lisa PaganiClinical Proteomics and Metabolomics Unit, Department of Medicine and Surgery, University of Milano-Bicocca, 20854 Monza, Italy.ORCID 0000-0002-9870-932X
Clizia ChinelloClinical Proteomics and Metabolomics Unit, Department of Medicine and Surgery, University of Milano-Bicocca, 20854 Monza, Italy.ORCID 0000-0002-7921-7768
Paolo PrevitaliClinical Proteomics and Metabolomics Unit, Department of Medicine and Surgery, University of Milano-Bicocca, 20854 Monza, Italy.
Andrew SmithClinical Proteomics and Metabolomics Unit, Department of Medicine and Surgery, University of Milano-Bicocca, 20854 Monza, Italy.ORCID 0000-0001-6530-6113
Gino VillettiExperimental Pharmacology & Translational Science Department, Chiesi Farmaceutici S.p.A., 43122 Parma, Italy.
Matteo ZoboliDepartment of Veterinary Science, University of Parma, 43122 Parma, Italy.ORCID 0000-0002-1299-5127
Francesca RavanettiDepartment of Veterinary Science, University of Parma, 43122 Parma, Italy.ORCID 0000-0001-8729-3237
Franco Fabio StellariExperimental Pharmacology & Translational Science Department, Chiesi Farmaceutici S.p.A., 43122 Parma, Italy.ORCID 0000-0002-8855-7297
Fulvio MagniClinical Proteomics and Metabolomics Unit, Department of Medicine and Surgery, University of Milano-Bicocca, 20854 Monza, Italy.ORCID 0000-0002-8663-0374
Isabella PigaClinical Proteomics and Metabolomics Unit, Department of Medicine and Surgery, University of Milano-Bicocca, 20854 Monza, Italy.ORCID 0000-0001-8221-2493

Funding

FAR 2017-2021 FAR 2017-2021Fondazione Gigi & Pupa Ferrari Onlus Fondazione Gigi & Pupa Ferrari OnlusRegione Lombardia regional law n° 9/2020, resolution n° 3776/2020
6 · The paper itself

Abstract

Idiopathic pulmonary fibrosis (IPF) is a chronic lung disease characterized by the aberrant accumulation of extracellular matrix in the lungs. nintedanib is one of the two FDA-approved drugs for IPF treatment; however, the exact pathophysiological mechanisms of fibrosis progression and response to therapy are still poorly understood. In this work, the molecular fingerprint of fibrosis progression and response to nintedanib treatment have been investigated by mass spectrometry-based bottom-up proteomics in paraffin-embedded lung tissues from bleomycin-induced (BLM) pulmonary fibrosis mice. Our proteomics results unveiled that (i) samples clustered depending on the tissue fibrotic grade (mild, moderate, and severe) and not on the time course after BLM treatment; (ii) the dysregulation of different pathways involved in fibrosis progression such as the complement coagulation cascades, advanced glycation end products (AGEs) and their receptors (RAGEs) signaling, the extracellular matrix-receptor interaction, the regulation of actin cytoskeleton, and ribosomes; (iii) Coronin 1A (Coro1a) as the protein with the highest correlation when evaluating the progression of fibrosis, with an increased expression from mild to severe fibrosis; and (iv) a total of 10 differentially expressed proteins (

Indexed as

BleomycinIdiopathic Pulmonary FibrosisAnimalsFibrosisLungMiceProteomicsBleomycinbleomycin mouse modelbottom-up mass spectrometryCoronin-1Alactate dehydrogenase Blung fibrosisnintedanibproteomics

Identifiers

PMID36901840
PMCPMC10002924

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read57
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.