Evidence map›Paper›PMID 36847936›Full record

ReviewMolecular neurobiology2023

Epigenetic Regulation of Ferroptosis in Central Nervous System Diseases.

Ting Lan, Ting Ting Sun, Chao Wei, Tian Cheng, Fei Yang, Jian-Nan Zhang, Qian Li

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular neurobiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
8.3field-weighted citation impact, top 2% 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

21 citing papers in PubMed, 32 citations in OpenAlex.

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  11. Mechanism of Ferroptosis and Its Role in Disease Development.International journal of biological sciences · 2025
    Review
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  13. Article
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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.

Ting Lan *Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Capital Medical University, Beijing, 100069, China.
Ting Ting Sun *Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Capital Medical University, Beijing, 100069, China.
Chao WeiDepartment of Neurobiology, School of Basic Medical Sciences, Capital Medical University, Beijing, 100069, China.
Tian ChengDepartment of Orthopedic, The 1st Affiliated Hospital of Zhengzhou University, 450052, Henan, China.
Fei YangDepartment of Neurobiology, School of Basic Medical Sciences, Capital Medical University, Beijing, 100069, China.
Jian-Nan ZhangDepartment of Neurobiology, School of Basic Medical Sciences, Capital Medical University, Beijing, 100069, China. jnzhang86@ccmu.edu.cn.ORCID http://orcid.org/0000-0001-5200-7368
Qian LiDepartment of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Capital Medical University, Beijing, 100069, China. qianli@ccmu.edu.cn.ORCID http://orcid.org/0000-0003-0359-5604
Capital Medical University · CNZhengzhou University · CN

Funding

Beijing Municipal Commission of Education KZ202010025033National Natural Science Foundation of China 32070735National Natural Science Foundation of China 81971037Science and Technology Project of Beijing Municipal Education Commission KM201910025030
6 · The paper itself

Abstract

Ferroptosis, a newly identified form of cell death, is characterized by iron overload and accumulation of lipid reactive oxygen species. Inactivation of pathways, such as glutathione/glutathione peroxidase 4, NAD(P)H/ferroptosis suppressor protein 1/ubiquinone, dihydroorotate dehydrogenase/ubiquinol, or guanosine triphosphate cyclohydrolase-1/6(R)-L-erythro-5,6,7,8-tetrahydrobiopterin pathways, have been found to induce ferroptosis. The accumulating data suggest that epigenetic regulation can determine cell sensitivity to ferroptosis at both the transcriptional and translational levels. While many of the effectors that regulate ferroptosis have been mapped, epigenetic regulation in ferroptosis is not yet fully understood. Neuronal ferroptosis is a driver in several central nervous system (CNS) diseases, such as stroke, Parkinson's disease, traumatic brain injury, and spinal cord injury, and thus, research on how to inhibit neuronal ferroptosis is required to develop novel therapies for these diseases. In this review, we have summarized epigenetic regulation of ferroptosis in these CNS diseases, focusing in particular on DNA methylation, non-coding RNA regulation, and histone modification. Understanding epigenetic regulation in ferroptosis will hasten the development of promising therapeutic strategies in CNS diseases associated with ferroptosis.

Indexed as

FerroptosisStrokeCell DeathEpigenesis, GeneticHumansLipid PeroxidationReactive Oxygen SpeciesReactive Oxygen SpeciesCentral nervous system diseasesEpigeneticsFerroptosisParkinson’s diseaseStrokeTraumatic brain injury

Identifiers

PMID36847936
OpenAlexW4322496398

What OpenQuestion holds

Textmetadata
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.