Evidence map›Paper›PMID 40649983›Full record

ReviewInternational journal of molecular sciences2025

Therapeutic Prospects of αv Integrins Inhibition in Fibrotic Lung Diseases and Carcinogenesis.

Eugenija Leonidovna Golovina, Veronika Vladimirovna Kochubey, Marina Alekseevna Shabanova, Darya Maksimovna Chekhvalova, Valentina Alexandrovna Serebryakova, Evgenii Germanovich Skurikhin, Olga Evgenievna Vaizova, Sergey Georgievich Morozov, Aslan Amirkhanovich Kubatiev, Alexander Mikhaylovich Dygai

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. The importance of mechanical forces in chronic respiratory diseases.European respiratory review : an official journal of the European Respiratory Society · 2026
    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

10 authors.

Eugenija Leonidovna GolovinaDepartment of Pharmacology, Siberian State Medical University, Ministry of Health of the Russian Federation, Tomsk 634050, Russia.
Veronika Vladimirovna KochubeyDepartment of Pharmacology, Siberian State Medical University, Ministry of Health of the Russian Federation, Tomsk 634050, Russia.ORCID 0009-0003-8743-5022
Marina Alekseevna ShabanovaDepartment of Pharmacology, Siberian State Medical University, Ministry of Health of the Russian Federation, Tomsk 634050, Russia.
Darya Maksimovna ChekhvalovaDepartment of Pharmacology, Siberian State Medical University, Ministry of Health of the Russian Federation, Tomsk 634050, Russia.
Valentina Alexandrovna SerebryakovaDepartment of Pharmacology, Siberian State Medical University, Ministry of Health of the Russian Federation, Tomsk 634050, Russia.
Evgenii Germanovich SkurikhinLaboratory of Regulation of Reparative Processes, Institute of General Pathology and Pathophysiology, Moscow 125315, Russia.ORCID 0000-0001-7445-4767
Olga Evgenievna VaizovaDepartment of Pharmacology, Siberian State Medical University, Ministry of Health of the Russian Federation, Tomsk 634050, Russia.
Sergey Georgievich MorozovLaboratory of Regulation of Reparative Processes, Institute of General Pathology and Pathophysiology, Moscow 125315, Russia.
Aslan Amirkhanovich KubatievLaboratory of Regulation of Reparative Processes, Institute of General Pathology and Pathophysiology, Moscow 125315, Russia.
Alexander Mikhaylovich DygaiLaboratory of Regulation of Reparative Processes, Institute of General Pathology and Pathophysiology, Moscow 125315, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The uncontrolled fibrosis of lung tissue can lead to premature death in patients suffering from idiopathic pulmonary fibrosis (IPF), and it complicates the course of chronic obstructive pulmonary disease (COPD) and emphysema. It is also a risk factor for developing lung cancer. Antifibrotic drugs, such as nantedanib and pirfenidone, are able to slow down the progression of pulmonary fibrosis, but more effective treatment is still needed to reverse it. Studies on the pathogenesis of tissue fibrosis have demonstrated that integrins play a crucial role affecting the development of pulmonary fibrosis, for example, by activating transforming growth factor-β (TGF-β). Taking the above into consideration, targeting specific integrins could offer promising opportunities for managing fibroplastic changes in lung tissue. Integrins are a type of transmembrane molecule that mediate interactions between cells and extracellular matrix (ECM) molecules. This review discusses the role of integrins in the pathogeneses of respiratory diseases and carcinogenesis, as well as presents promising approaches to the drug therapy of pulmonary fibrosis of various etiologies based on integrin inhibition.

Indexed as

CarcinogenesisIdiopathic Pulmonary FibrosisIntegrin alphaVLung NeoplasmsPulmonary FibrosisAnimalsHumansIntegrin alphaVchronic obstructive pulmonary diseaseidiopathic pulmonary fibrosislung cancerαv integrin

Identifiers

PMID40649983
PMCPMC12249868

What OpenQuestion holds

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Registered trials

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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.