Evidence map›Paper›PMID 37214555›Full record

ArticleMaterials today. Bio2023

Albumin-based formononetin nanomedicines for lung injury and fibrosis therapy via blocking macrophage pyroptosis.

Boshu Ouyang, Lingling Deng, Fangyong Yang, Hanlin Shi, Na Wang, Weifeng Tang, Xi Huang, Yaolong Zhou, Hang Yu, Ying Wei and 1 more

Open access · goldAbstract read
In one paragraph

Article in Materials today. Bio, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.6field-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

17 citing papers in PubMed, 30 citations in OpenAlex.

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  14. Effective delivery of miR-511-3p with mannose-decorated exosomes with RNA nanoparticles confers protection against asthma.Journal of controlled release : official journal of the Controlled Release Society · 2024
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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

11 authors at 1 institution in 1 country.

Boshu OuyangDepartment of Integrative Medicine, Huashan Hospital, Fudan University, Shanghai, 200040, PR China.
Lingling DengDepartment of Integrative Medicine, Huashan Hospital, Fudan University, Shanghai, 200040, PR China.
Fangyong YangDepartment of Integrative Medicine, Huashan Hospital, Fudan University, Shanghai, 200040, PR China.
Hanlin ShiDepartment of Integrative Medicine, Huashan Hospital, Fudan University, Shanghai, 200040, PR China.
Na WangDepartment of Integrative Medicine, Huashan Hospital, Fudan University, Shanghai, 200040, PR China.
Weifeng TangDepartment of Integrative Medicine, Huashan Hospital, Fudan University, Shanghai, 200040, PR China.
Xi HuangDepartment of Integrative Medicine, Huashan Hospital, Fudan University, Shanghai, 200040, PR China.
Yaolong ZhouDepartment of Integrative Medicine, Huashan Hospital, Fudan University, Shanghai, 200040, PR China.
Hang YuDepartment of Integrative Medicine, Huashan Hospital, Fudan University, Shanghai, 200040, PR China.
Ying WeiDepartment of Integrative Medicine, Huashan Hospital, Fudan University, Shanghai, 200040, PR China.
Jingcheng DongDepartment of Integrative Medicine, Huashan Hospital, Fudan University, Shanghai, 200040, PR China.
Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pulmonary fibrosis that occurs following lung injury is a progressive and fatal disease since continual damage to lung tissue triggers the dysregulated inflammation response and accompanying abnormal healing process. Pyroptosis of alveolar macrophages has been found to play an essential role in the deterioration of lung injury and fibrosis. However, the lack of inhibitors against this inflammatory cell death in macrophages and the dense stroma pose major barriers to lung injury and fibrosis treatment. Herein, we developed an albumin-based nanoformulation to realize active delivery of formononetin (FMN) to improve the treatment of lung injury and fibrosis. The obtained nanoparticle, FMN@BSA NPs, could efficiently accumulate at the impaired lesion benefiting from the leaky vasculatures and the affinity between albumin and the overexpressed SPARC protein. Through blocking the NLRP3 inflammasome-involved pyroptosis process of macrophages, FMN@BSA NPs remarkably improved lung function and prolonged animal survival in the bleomycin (BLM)-induced lung injury and fibrosis model without noticeable side effects. Meanwhile, we proved FMN as a pyroptosis inhibitor and the corresponding lipid metabolism-related mechanisms through multi-omics analysis. This study first employed an albumin-based nanoparticle to deliver the pyroptosis inhibitor to the impaired lung tissue actively, providing a promising strategy for lung injury and fibrosis treatment.

Indexed as

FibrosisFormononetinLung injuryMacrophage pyroptosisNLRP3SPARC

Identifiers

PMID37214555
PMCPMC10193015
OpenAlexW4366978776

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.