Evidence map›Paper›PMID 37324946›Full record

ReviewInternational journal of biological sciences2023

The crosstalk between ferroptosis and mitochondrial dynamic regulatory networks.

Jie Li, Yu-Chen Jia, Yi-Xuan Ding, Jian Bai, Feng Cao, Fei Li

Open access · goldAbstract readReview
In one paragraph

Review in International journal of biological sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 205 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
205citing papers in PubMed, 1 pooled it
67.7field-weighted citation impact, top 1% 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

205 citing papers in PubMed, 1 synthesis or guideline pooled it, 262 citations in OpenAlex.

  1. Pooled it
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  5. Cancer biology & therapy · 2026
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145 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 2 countries.

Jie LiDepartment of General Surgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Yu-Chen JiaDepartment of General Surgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Yi-Xuan DingDepartment of General Surgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Jian BaiDepartment of General Surgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Feng CaoDepartment of General Surgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Fei LiDepartment of General Surgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Capital Medical University · CNPancreas Centre (Canada) · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ferroptosis is an iron-driven cell death modality characterized by iron accumulation and excessive lipid peroxidation. Ferroptosis is closely related to mitochondrial function, as indicated by studies showing that mitochondrial dysfunction and damage promote oxidative stress, which in turn induces ferroptosis. Mitochondria play crucial roles in cellular homeostasis, and abnormalities in their morphology and function are closely associated with the development of many diseases. Mitochondria are highly dynamic organelles, and their stability is maintained through a series of regulatory pathways. Mitochondrial homeostasis is dynamically regulated, mainly via key processes such as mitochondrial fission, mitochondrial fusion and mitophagy; however, mitochondrial processes are prone to dysregulation. Mitochondrial fission and fusion and mitophagy are intimately related to ferroptosis. Therefore, investigations into the dynamic regulation of mitochondrial processes during ferroptosis are important to provide a better understanding of the development of disease. In this paper, we systematically summarized changes in ferroptosis, mitochondrial fission and fusion and mitophagy to promote an in-depth understanding of the mechanism underlying ferroptosis and provide a corresponding reference for the treatment of related diseases.

Indexed as

FerroptosisIronMitochondriaMitochondrial DynamicsMitophagyReactive Oxygen SpeciesIronReactive Oxygen Speciesferroptosismitochondrial fissionmitochondrial fusionmitochondrial homeostasismitophagyreactive oxygen species

Identifiers

PMID37324946
PMCPMC10266069
OpenAlexW4379384673

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.