Evidence map›Paper›PMID 35220409›Full record

ArticleCell death discovery2022

NVP-AUY922 alleviates radiation-induced lung injury via inhibition of autophagy-dependent ferroptosis.

Li Li, Dongming Wu, Shihua Deng, Jin Li, Feng Zhang, Ye Zou, Ting Zhang, Ying Xu

Open access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
9.6field-weighted citation impact, top 1% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 65 citations in OpenAlex.

  1. Pooled it
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  10. Role of Ferroptosis on Lung Epithelial Cells in Disease Progression and Treatment: A Review.Medical science monitor : international medical journal of experimental and clinical research · 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

8 authors at 1 institution in 1 country.

Li Li *School of Clinical Medicine, Chengdu Medical College, Chengdu, Sichuan, 610500, P.R. China.
Dongming Wu *School of Clinical Medicine, Chengdu Medical College, Chengdu, Sichuan, 610500, P.R. China.
Shihua Deng *School of Clinical Medicine, Chengdu Medical College, Chengdu, Sichuan, 610500, P.R. China.
Jin LiSchool of Clinical Medicine, Chengdu Medical College, Chengdu, Sichuan, 610500, P.R. China.
Feng ZhangSchool of Clinical Medicine, Chengdu Medical College, Chengdu, Sichuan, 610500, P.R. China.
Ye ZouSchool of Clinical Medicine, Chengdu Medical College, Chengdu, Sichuan, 610500, P.R. China.
Ting ZhangSchool of Clinical Medicine, Chengdu Medical College, Chengdu, Sichuan, 610500, P.R. China.
Ying XuSchool of Clinical Medicine, Chengdu Medical College, Chengdu, Sichuan, 610500, P.R. China. yingxu825@126.com.ORCID http://orcid.org/0000-0001-9570-8666
Chengdu Medical College · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81802955National Natural Science Foundation of China (National Science Foundation of China) 81972977
6 · The paper itself

Abstract

Radiation-induced lung injury (RILI) is a common complication of radiotherapy for which no effective interventions are available. NVP-AUY922, a resorcinylic isoxazole amide drug, exhibits anti-inflammatory, immunomodulatory, and therapeutic effects against various types of cancers. In this study, we explore the role and underlying mechanisms of NVP-AUY922 in the treatment of RILI. We established a model of BEAS-2B cell injury and a mouse model of RILI. Cell proliferation, death, gross weight, and survival rates of mice, and histological parameters were assessed. Additionally, inflammation-related indices and indicators related to ferroptosis were evaluated. Furthermore, immunofluorescence and co-immunoprecipitation were used to determine the interaction between GPX4, LAMP-2A, and HSC70. NVP-AUY922 significantly ameliorated radiation-induced lung tissue damage, inflammatory cell infiltration, proinflammatory cytokine release, and lung epithelial BEAS-2B cell damage. NVP-AUY922 markedly limited the activation of ferroptosis, which is involved in RILI. Mechanistically, NVP-AUY922 prevented chaperone-mediated autophagy of the GPX4 pathway in vitro and in vivo, and the autophagy inhibitor Baf-A1 significantly increased the level of GPX4 and alleviated lung inflammation. NVP-AUY922 can alleviate RILI by inhibiting chaperone-mediated lysosomal degradation of GPX4, demonstrating its potential as a novel protective agent against RILI.

Identifiers

PMID35220409
PMCPMC8882174
OpenAlexW4214704244

What OpenQuestion holds

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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.