Evidence map›Paper›PMID 33077618›Full record

ReviewThorax2021

Role of unfolded proteins in lung disease.

Kirsty L Bradley, Clare A Stokes, Stefan J Marciniak, Lisa C Parker, Alison M Condliffe

Open access · bronzeAbstract readReview
In one paragraph

Review in Thorax, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 5% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 67 citations in OpenAlex.

  1. Pooled it
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  9. Frontiers in immunology · 2025
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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

5 authors at 2 institutions in 1 country.

Kirsty L BradleyDepartment of Infection, Immunity and Cardiovascular Diseases, The University of Sheffield, Sheffield, UK.
Clare A StokesDepartment of Infection, Immunity and Cardiovascular Diseases, The University of Sheffield, Sheffield, UK.
Stefan J Marciniak *Medicine, University of Cambridge, Cambridge, UK.ORCID 0000-0001-8472-7183
Lisa C Parker *Department of Infection, Immunity and Cardiovascular Diseases, The University of Sheffield, Sheffield, UK.
Alison M Condliffe *Department of Infection, Immunity and Cardiovascular Diseases, The University of Sheffield, Sheffield, UK a.m.condliffe@sheffield.ac.uk.ORCID 0000-0002-6697-8648
University of Sheffield · GBUniversity of Cambridge · GB

Funding

Medical Research Council G1002610Medical Research Council MR/R009120/1Medical Research Council MR/V028669/1
6 · The paper itself

Abstract

The lungs are exposed to a range of environmental toxins (including cigarette smoke, air pollution, asbestos) and pathogens (bacterial, viral and fungal), and most respiratory diseases are associated with local or systemic hypoxia. All of these adverse factors can trigger endoplasmic reticulum (ER) stress. The ER is a key intracellular site for synthesis of secretory and membrane proteins, regulating their folding, assembly into complexes, transport and degradation. Accumulation of misfolded proteins within the lumen results in ER stress, which activates the unfolded protein response (UPR). Effectors of the UPR temporarily reduce protein synthesis, while enhancing degradation of misfolded proteins and increasing the folding capacity of the ER. If successful, homeostasis is restored and protein synthesis resumes, but if ER stress persists, cell death pathways are activated. ER stress and the resulting UPR occur in a range of pulmonary insults and the outcome plays an important role in many respiratory diseases. The UPR is triggered in the airway of patients with several respiratory diseases and in corresponding experimental models. ER stress has been implicated in the initiation and progression of pulmonary fibrosis, and evidence is accumulating suggesting that ER stress occurs in obstructive lung diseases (particularly in asthma), in pulmonary infections (some viral infections and in the setting of the cystic fibrosis airway) and in lung cancer. While a number of small molecule inhibitors have been used to interrogate the role of the UPR in disease models, many of these tools have complex and off-target effects, hence additional evidence (eg, from genetic manipulation) may be required to support conclusions based on the impact of such pharmacological agents. Aberrant activation of the UPR may be linked to disease pathogenesis and progression, but at present, our understanding of the context-specific and disease-specific mechanisms linking these processes is incomplete. Despite this, the ability of the UPR to defend against ER stress and influence a range of respiratory diseases is becoming increasingly evident, and the UPR is therefore attracting attention as a prospective target for therapeutic intervention strategies.

Indexed as

Endoplasmic Reticulum StressHumansLung DiseasesMembrane ProteinsSignal TransductionMembrane Proteinsairway epitheliumasthmainnate immunityrespiratory infectionviral infection

Identifiers

PMID33077618
PMCPMC7803888
OpenAlexW3092972404

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.