Evidence map›Paper›PMID 34630843›Full record

ReviewOxidative medicine and cellular longevity2021

Targeting Ferroptosis for Lung Diseases: Exploring Novel Strategies in Ferroptosis-Associated Mechanisms.

Tian-Liang Ma, Yong Zhou, Ci Wang, Lu Wang, Jing-Xian Chen, Hui-Hui Yang, Chen-Yu Zhang, Yong Zhou, Cha-Xiang Guan

Open access · hybridAbstract readReview
In one paragraph

Review in Oxidative medicine and cellular longevity, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.1field-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

25 citing papers in PubMed, 35 citations in OpenAlex.

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  19. Ferroptosis-related metabolic mechanism and nanoparticulate anticancer drug delivery systems based on ferroptosis.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2023
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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

9 authors at 2 institutions in 1 country.

Tian-Liang MaDepartment of Physiology, School of Basic Medical Science, Central South University, Changsha, Hunan 410078, China.
Yong ZhouDepartment of Physiology, School of Basic Medical Science, Central South University, Changsha, Hunan 410078, China.
Ci WangDepartment of Cardiovascular Medicine, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, National Clinical Research Center for Chinese Medicine Acupuncture and Moxibustion, Tianjin University of Traditional Chinese Medicine, Tianjin 300381, China.
Lu WangDepartment of Cardiology, The Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, China.
Jing-Xian ChenDepartment of Cardiology, The Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, China.
Hui-Hui YangDepartment of Physiology, School of Basic Medical Science, Central South University, Changsha, Hunan 410078, China.
Chen-Yu ZhangDepartment of Physiology, School of Basic Medical Science, Central South University, Changsha, Hunan 410078, China.
Yong ZhouDepartment of Physiology, School of Basic Medical Science, Central South University, Changsha, Hunan 410078, China.ORCID https://orcid.org/0000-0002-7348-2376
Cha-Xiang GuanDepartment of Physiology, School of Basic Medical Science, Central South University, Changsha, Hunan 410078, China.ORCID https://orcid.org/0000-0002-8505-8724
Central South University · CNFirst Teaching Hospital of Tianjin University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ferroptosis is an iron-dependent regulated necrosis characterized by the peroxidation damage of lipid molecular containing unsaturated fatty acid long chain on the cell membrane or organelle membrane after cellular deactivation restitution system, resulting in the cell membrane rupture. Ferroptosis is biochemically and morphologically distinct and disparate from other forms of regulated cell death. Recently, mounting studies have investigated the mechanism of ferroptosis, and numerous proteins play vital roles in regulating ferroptosis. With detailed studies, emerging evidence indicates that ferroptosis is found in multiple lung diseases, demonstrating that ferroptosis appears to be particularly important for lung diseases. The mounting interest in ferroptosis drugs specifically targeting the ferroptosis mechanism holds substantial therapeutic promise in lung diseases. The present review emphatically summarizes the functions and integrated molecular mechanisms of ferroptosis in various lung diseases, proposing that multiangle regulation of ferroptosis might be a promising strategy for the clinical treatment of lung diseases.

Indexed as

AnimalsAutophagyFerroptosisHumansIronLipid PeroxidationLung DiseasesMolecular Targeted TherapyNecrosisPyroptosisReactive Oxygen SpeciesTreatment OutcomeIronReactive Oxygen Species

Identifiers

PMID34630843
PMCPMC8494591
OpenAlexW3204615893

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.