Evidence map›Paper›PMID 39946006›Full record

ArticleInflammation2025

SIRT5 Alleviated Eosinophilic Asthma Through ROS Inhibition and Nrf2/HO-1 Activation.

Yuwei Xie, Yingzhi He, Juan Liang, Jie Liu, Chuanghong Ke, Xiaohuan Mo, Cizheng Zeng, Sijie Wang, Xuemei Chen, Dang Ao and 2 more

Abstract read
In one paragraph

Article in Inflammation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
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  3. Article
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

12 authors.

Yuwei Xie *Department of Pediatrics, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, Guangdong, China.
Yingzhi He *Department of Pediatrics, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, Guangdong, China.
Juan Liang *Department of Pediatrics, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, Guangdong, China.
Jie LiuExperimental Animal Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, Guangdong, China.
Chuanghong KeDepartment of Pediatrics, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, Guangdong, China.
Xiaohuan MoDepartment of Pediatrics, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, Guangdong, China.
Cizheng ZengDepartment of Pediatrics, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, Guangdong, China.
Sijie WangClinical Research and Experimental Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, Guangdong, China.
Xuemei ChenDepartment of Pediatrics, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, Guangdong, China.
Dang AoDepartment of Pediatrics, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, Guangdong, China. aodang@21cn.com.
Jinfeng TangClinical Research and Experimental Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, Guangdong, China. abcdtangjf@163.com.
Wen LiDepartment of Pediatrics, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, Guangdong, China. liwen410@163.com.

Funding

Guangdong Natural Science Foundation of China 2023A1515012755National Natural Science Foundation of China 32100602the high-level talents scientific research start-up funds of the Affiliated Hospital of Guangdong Medical University GCC2021009
6 · The paper itself

Abstract

Asthma is a prevalent chronic disease with high morbidity and mortality in both children and adults, imposing a burden on the physical and mental well-being of patients, as well as their families. Inhaled corticosteroids and long-acting β2 agonists are mostly used to control asthma, these therapies are not suitable for patients with severe asthma. Approximately 80% of severe uncontrolled asthma cases are classified as eosinophilic asthma (EA). Oxidative stress and inflammation play crucial roles in the pathology and development of asthma, with SIRT5 being important in the process of anti-oxidation and anti-inflammation. However, little is known about the role of SIRT5 in EA and its regulatory mechanism on substrate protein and biological function. In this study, we investigated the role of SIRT5 in ovalbumin (OVA)-induced EA mouse models and house dust mite (HDM)-induced asthmatic cell models, while exploring its potential mechanisms. We found that SIRT5 alleviated EA by inhibiting reactive oxygen species and activating Nrf2/HO-1 pathways. Interestingly, overexpression of SIRT5 attenuated the inflammatory response in EA. Taken together, these results suggest that SIRT5 may serve as a promising target for managing asthma symptoms.

Indexed as

AsthmaHeme Oxygenase-1NF-E2-Related Factor 2Reactive Oxygen SpeciesSirtuinsAnimalsDisease Models, AnimalHumansMembrane ProteinsMiceMice, Inbred BALB COvalbuminOxidative StressHeme Oxygenase-1Hmox1 protein, mouseMembrane ProteinsNfe2l2 protein, mouseNF-E2-Related Factor 2OvalbuminReactive Oxygen SpeciesSirtuinsEosinophilic asthmaNrf2/HO-1Oxidative stressROSSIRT5

Identifiers

PMID39946006
PMCPMC12596428

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.