Evidence map›Paper›PMID 35596212›Full record

ArticleRespiratory research2022

NecroX-5 ameliorates bleomycin-induced pulmonary fibrosis via inhibiting NLRP3-mediated epithelial-mesenchymal transition.

Li Min, Zhang Shu-Li, Yuan Feng, Hu Han, Li Shao-Jun, Tong Sheng-Xiong, Tian Jia-Yu, Fang Xiang-Zhi, Feng Dan

Open access · goldAbstract read
In one paragraph

Article in Respiratory research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. Inflammasomes in respiratory diseases: from disease pathogenesis to drug development and use of multi-omics.European respiratory review : an official journal of the European Respiratory Society · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Regulation of alveolar macrophage death in pulmonary fibrosis: a review.Apoptosis : an international journal on programmed cell death · 2023
    Review
  9. 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

9 authors at 2 institutions in 1 country.

Li Min *Department of Pain Management, Wuhan First Hospital, Wuhan, China.
Zhang Shu-Li *Department of Pain Management, Wuhan First Hospital, Wuhan, China.
Yuan FengDepartment of Pain Management, Wuhan First Hospital, Wuhan, China.
Hu HanDepartment of Pain Management, Wuhan First Hospital, Wuhan, China.
Li Shao-JunDepartment of Pain Management, Wuhan First Hospital, Wuhan, China.
Tong Sheng-XiongDepartment of Pain Management, Wuhan First Hospital, Wuhan, China.
Tian Jia-YuDepartment of Pain Management, Wuhan First Hospital, Wuhan, China.
Fang Xiang-ZhiDepartment of Critical Care Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Feng DanDepartment of Pain Management, Wuhan First Hospital, Wuhan, China. fengdan_pain@126.com.
Wuhan Third Hospital · CNHuazhong University of Science and Technology · CN

Funding

Project of Wuhan Health and Family Planning Commission WX19C13, WX17D04
6 · The paper itself

Abstract

backgroundPulmonary fibrosis is a progressive and usually lethal pulmonary disease. Despite considerable research efforts, no effective therapeutic strategy for pulmonary fibrosis has been developed. NecroX-5 has been reported to possess anti-inflammatory, anti-oxidative and anti-tumor activities. In the present study, we aimed to determine whether NecroX-5 exhibits antifibrotic property in bleomycin (BLM)-induced pulmonary fibrosis.

resultsWe found that pre-treatment with NecroX-5 alleviated inflammatory response, reduced oxidative stress, inhibited epithelial-mesenchymal transition (EMT), and ameliorated pulmonary fibrosis in vivo and in vitro. Our data further indicated that NecroX-5 substantially reduced activation of NLRP3 inflammasome and TGF-β1/Smad2/3 signaling in vivo and in vitro. Additionally, NLRP3 overexpression significantly reversed the protective effects of NecroX-5 in lung epithelial cells exposed to BLM.

conclusionsOverall, our results demonstrate the potent antifibrotic properties of NecroX-5 and its therapeutic potential for pulmonary fibrosis.

Indexed as

Epithelial-Mesenchymal TransitionHeterocyclic Compounds, 4 or More RingsNLR Family, Pyrin Domain-Containing 3 ProteinPulmonary FibrosisSulfonesAnimalsBleomycinMiceTransforming Growth Factor beta1BleomycinHeterocyclic Compounds, 4 or More RingsNecroX-5NLR Family, Pyrin Domain-Containing 3 ProteinSulfonesTransforming Growth Factor beta1EMTFibrosisLung injuryNecroX-5NLRP3

Identifiers

PMID35596212
PMCPMC9121617
OpenAlexW4280648639

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.