Evidence map›Paper›PMID 38102663›Full record

ReviewCell & bioscience2023

Ferroptosis in cardiovascular diseases: role and mechanism.

Qi Zhang, Yuhao Luo, Lin Peng, Xi Rong, Yingxue Liu, Jiafu Li, Jing Luo

Open access · goldAbstract readReview
In one paragraph

Review in Cell & bioscience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
6.2field-weighted citation impact, top 3% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

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  19. Stem Cell Therapy against Ischemic Heart Disease.International journal of molecular sciences · 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

7 authors at 2 institutions in 1 country.

Qi Zhang *Department of Cardiology, The Affiliated Hospital of Southwest Medical University, Luzhou, China.
Yuhao Luo *Department of Oncology, The Affiliated Hospital of Southwest Medical University, Luzhou, China.
Lin PengDepartment of Bone and Joint Surgery, The Affiliated Hospital of Southwest Medical University, Luzhou, China.
Xi RongDepartment of Cardiology, The Affiliated Hospital of Southwest Medical University, Luzhou, China.
Yingxue LiuDepartment of Cardiology, The Affiliated Hospital of Southwest Medical University, Luzhou, China.
Jiafu LiDepartment of Cardiology, The Affiliated Hospital of Southwest Medical University, Luzhou, China. lijiafu198948@swmu.edu.cn.
Jing LuoDepartment of Cardiology, The Affiliated Hospital of Southwest Medical University, Luzhou, China. luojing1991@swmu.edu.cn.ORCID http://orcid.org/0009-0004-9594-4967
Affiliated Hospital of Southwest Medical University · CNSouthwest Medical University · CN

Funding

Affiliated Hospital of Southwest Medical University 00031742Affiliated Hospital of Southwest Medical University 2021ZKQN093National Natural Science Foundation of China 81903000Natural Science Foundation of Sichuan Province 2023NSFSC1846Sichuan Province Science and Technology Support Program 2022YFS0636-B4Sichuan Province Science and Technology Support Program 2022YFS0636-C4
6 · The paper itself

Abstract

In multicellular organisms, regulatory cell death is a crucial aspect of growth and development. Ferroptosis, which was postulated roughly ten years ago, is a mode of cell death that differs from apoptosis, autophagy, and pyrodeath. This distinct pattern of cell death is triggered by an imbalance between oxidants and antioxidants and strongly associated with the metabolism of iron, lipids, amino acids, and glutathione. A growing body of research has implicated ferroptosis in the incidence and progression of many organ traumas and degenerative diseases. Recently, ferroptosis has gained attention as a crucial regulatory mechanism underlying the initiation and development of a variety of cardiovascular diseases, including myocardial ischemia/reperfusion injury, cardiomyopathy, arrhythmia, chemotherapy, and Corona Virus-2-induced cardiac injury. Pharmacological therapies that inhibit ferroptosis have great potential for the management of cardiovascular disorders. This review discusses the prevalence and regulatory mechanisms of ferroptosis, effect of ferroptosis on the immune system, significance of ferroptosis in cardiovascular diseases, and potential therapeutic value of regulating ferroptosis in a variety of heart diseases.

Indexed as

Cardiovascular diseaseCorona Virus-2FerroptosisRegulated cell death

Identifiers

PMID38102663
PMCPMC10724928
OpenAlexW4389818430

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.