Evidence map›Paper›PMID 34502225›Full record

ReviewInternational journal of molecular sciences2021

Extracellular Heat Shock Proteins as Therapeutic Targets and Biomarkers in Fibrosing Interstitial Lung Diseases.

Julie Tanguy, Lenny Pommerolle, Carmen Garrido, Martin Kolb, Philippe Bonniaud, Françoise Goirand, Pierre-Simon Bellaye

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. The role of heat shock protein 90 in idiopathic pulmonary fibrosis: state of the art.European respiratory review : an official journal of the European Respiratory Society · 2025
    Review
  7. Article
  8. Article
  9. The Lung in Rheumatoid Arthritis-Friend or Enemy?International journal of molecular sciences · 2024
    Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Review
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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 3 institutions in 2 countries.

Julie TanguyTeam HSP-Pathies, INSERM U1231, 21000 Dijon, France.ORCID 0000-0003-1497-0852
Lenny PommerolleTeam HSP-Pathies, INSERM U1231, 21000 Dijon, France.
Carmen GarridoTeam HSP-Pathies, INSERM U1231, 21000 Dijon, France.
Martin KolbFirestone Institute for Respiratory Health, McMaster University, Hamilton, ON L8S 4L8, Canada.
Philippe BonniaudTeam HSP-Pathies, INSERM U1231, 21000 Dijon, France.
Françoise GoirandTeam HSP-Pathies, INSERM U1231, 21000 Dijon, France.
Pierre-Simon BellayeCentre de Référence Constitutif des Maladies Pulmonaires Rares de l'Adultes de Dijon, OrphaLung Network (RespiFil), University Hospital of Burgundy, 21000 Dijon, France.
Inserm · FRCentre Georges François Leclerc · FRMcMaster University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interstitial lung diseases (ILDs) include a large number of diseases and causes with variable outcomes often associated with progressive fibrosis. Although each of the individual fibrosing ILDs are rare, collectively, they affect a considerable number of patients, representing a significant burden of disease. Idiopathic pulmonary fibrosis (IPF) is the typical chronic fibrosing ILD associated with progressive decline in lung. Other fibrosing ILDs are often associated with connective tissues diseases, including rheumatoid arthritis-ILD (RA-ILD) and systemic sclerosis-associated ILD (SSc-ILD), or environmental/drug exposure. Given the vast number of progressive fibrosing ILDs and the disparities in clinical patterns and disease features, the course of these diseases is heterogeneous and cannot accurately be predicted for an individual patient. As a consequence, the discovery of novel biomarkers for these types of diseases is a major clinical challenge. Heat shock proteins (HSPs) are molecular chaperons that have been extensively described to be involved in fibrogenesis. Their extracellular forms (eHSPs) have been recently and successfully used as therapeutic targets or circulating biomarkers in cancer. The current review will describe the role of eHSPs in fibrosing ILDs, highlighting the importance of these particular stress proteins to develop new therapeutic strategies and discover potential biomarkers in these diseases.

Indexed as

AnimalsBiomarkersDisease ProgressionHeat-Shock ProteinsHumansIdiopathic Pulmonary FibrosisLung Diseases, InterstitialMolecular Targeted TherapyBiomarkersHeat-Shock Proteinsbiomarkerextracellular HSPheat shock proteinsinterstitial lung diseasesIPFlung fibrosis

Identifiers

PMID34502225
PMCPMC8430559
OpenAlexW3196784210

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.