Evidence map›Paper›PMID 34829907›Full record

ReviewBiomedicines2021

Ferroptosis as a Major Factor and Therapeutic Target for Neuroinflammation in Parkinson's Disease.

Chih-Jan Ko, Shih-Ling Gao, Tsu-Kung Lin, Pei-Yi Chu, Hung-Yu Lin

Open access · goldAbstract readReview
In one paragraph

Review in Biomedicines, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
5.3field-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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

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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

5 authors at 5 institutions in 1 country.

Chih-Jan KoDepartment of General Surgery, Changhua Christian Hospital, 135 Nanhsiao Street, Changhua 500, Taiwan.
Shih-Ling GaoDepartment of Nursing, Changhua Christian Hospital, 135 Nanhsiao Street, Changhua 500, Taiwan.
Tsu-Kung LinCenter for Mitochondrial Research and Medicine, Kaohsiung Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Kaohsiung 833, Taiwan.ORCID 0000-0001-6656-1319
Pei-Yi ChuCollege of Medicine, National Chung Hsing University, Taichung 402, Taiwan.ORCID 0000-0001-7336-2465
Hung-Yu LinResearch Assistant Center, Show Chwan Memorial Hospital, Changhua 500, Taiwan.ORCID 0000-0002-9035-5408
Chang Bing Show Chwan Memorial Hospital · TWChang Gung University · TWChanghua Christian Hospital · TWFu Jen Catholic University · TWKaohsiung Medical University · TW

Funding

Ministry of Science and Technology, Taiwan MOST 106-2314-B-442-001-MY3, MOST 109-2314-B-442-001- and MOST 109-2314-B-075B-002National Health Research Institutes, Taiwan NHRI-109BCCO-MF-202015-01Show Chwan Memorial Hospital, Taiwan SRD-109024 and SRD-109025
6 · The paper itself

Abstract

Mounting evidence suggests that ferroptosis is not just a consequence but also a fundamental contributor to the development and progression of Parkinson's disease (PD). Ferroptosis is characterized as iron-dependent regulated cell death caused by excessive lipid peroxidation, leading to plasma membrane rupture, release of damage-associated molecular patterns, and neuroinflammation. Due to the crucial role of intracellular iron in mediating the production of reactive oxygen species and the formation of lipid peroxides, ferroptosis is intimately controlled by regulators involved in many aspects of iron metabolism, including iron uptake, storage and export, and by pathways constituting the antioxidant systems. Translational and transcriptional regulation of iron homeostasis and redox status provide an integrated network to determine the sensitivity of ferroptosis. We herein review recent advances related to ferroptosis, ranging from fundamental mechanistic discoveries and cutting-edge preclinical animal studies, to clinical trials in PD and the regulation of neuroinflammation via ferroptosis pathways. Elucidating the roles of ferroptosis in the survival of dopaminergic neurons and microglial activity can enhance our understanding of the pathogenesis of PD and provide opportunities for the development of novel prevention and treatment strategies.

Indexed as

antioxidant defenseferroptosisironlipid peroxidationneuroinflammationParkinson’s disease

Identifiers

PMID34829907
PMCPMC8615560
OpenAlexW3213364147

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.