Evidence map›Paper›PMID 36243856›Full record

ArticleCurrent topics in microbiology and immunology2022

Developing PI3K Inhibitors for Respiratory Diseases.

E Fagone, M Fruciano, E Gili, G Sambataro, Carlo Vancheri

Abstract read
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In one paragraph

Article in Current topics in microbiology and immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
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  4. 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

5 authors at 1 institution in 1 country.

E FagoneDepartment of Clinical and Experimental Medicine, Regional Referral Center for Rare Lung Diseases, University Hospital "Policlinico G. Rodolico-San Marco", University of Catania, Catania, Italy.
M FrucianoDepartment of Clinical and Experimental Medicine, Regional Referral Center for Rare Lung Diseases, University Hospital "Policlinico G. Rodolico-San Marco", University of Catania, Catania, Italy.
E GiliDepartment of Clinical and Experimental Medicine, Regional Referral Center for Rare Lung Diseases, University Hospital "Policlinico G. Rodolico-San Marco", University of Catania, Catania, Italy.
G SambataroDepartment of Clinical and Experimental Medicine, Regional Referral Center for Rare Lung Diseases, University Hospital "Policlinico G. Rodolico-San Marco", University of Catania, Catania, Italy.
Carlo VancheriDepartment of Clinical and Experimental Medicine, Regional Referral Center for Rare Lung Diseases, University Hospital "Policlinico G. Rodolico-San Marco", University of Catania, Catania, Italy. vancheri@unict.it.
University of Catania · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A number of different experimental models using both non-selective and selective PI3K inhibitors have shown that many pathogenic steps of respiratory disorders, such as bronchial asthma, Chronic Obstructive Pulmonary Disease (COPD), Idiopathic Pulmonary Fibrosis (IPF), Acute Respiratory Distress Syndrome (ARDS) and Lung Cancer (LC) are, at least in part, regulated by the PI3K signaling pathway, suggesting that the inhibition of PI3K could represent an ideal therapeutic target for the treatment of respiratory diseases. This chapter summarizes the current state of the therapeutic strategies aimed to exploit the inhibition of PI3K in this context. In animal models of asthma, selective δ and γ inhibitors have shown to be effective, and when administered by inhalation, reasonably safe. Nevertheless, very few clinical trials have been performed so far. The efficacy of current traditional therapies for allergic bronchial asthma has likely diminished the need for new alternative treatments. Surprisingly, in COPD, where instead there is an urgent need for new and more effective therapeutic approaches, the number of clinical studies is still low and not capable yet, with the exception for an acceptable safety profile, to show a significant improvement of clinical outcomes. In IPF, a disease with a disappointing prognosis, PI3K inhibitors have been bound to a FAP ligand with the aim to selectively target myofibroblasts, showing to significantly reduce collagen production and the development of lung fibrosis in an animal model of lung fibrosis. Due to its role in cell activation and cell replication, the PI3K pathway is obviously largely involved in lung cancer. Several studies, currently ongoing, are testing the effect of PI3K inhibitors mainly in NSCLC. Some evidence in the treatment of cancer patients suggests the possibility that PI3K inhibitors may enhance the response to conventional treatment. The involvement of PI3Kδ in the modulation of airway neutrophil recruitment and bronchial epithelial functional alterations also suggest a potential role in the treatment of ARDS, but at the current state the ongoing trials are aimed to the treatment of ARDS in COVID-19 patients. In general, few clinical trials investigating PI3K inhibitors in respiratory disorders have been performed so far. This relatively new approach of treatment is just at its beginning and certainly needs further efforts and additional studies.

Indexed as

AsthmaCOVID-19Idiopathic Pulmonary FibrosisLung NeoplasmsPulmonary Disease, Chronic ObstructiveRespiratory Distress SyndromeAnimalsCollagenLigandsPhosphatidylinositol 3-KinasesCollagenLigandsPhosphatidylinositol 3-Kinases

Identifiers

PMID36243856
OpenAlexW4306361990

What OpenQuestion holds

Textmetadata
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.