Evidence map›Paper›PMID 37860583›Full record

ReviewFrontiers in molecular biosciences2023

Recent progress in the effect of ferroptosis of HSCs on the development of liver fibrosis.

Rui Tang, Jing Luo, Xiaoxia Zhu, Pengyu Miao, Hong Tang, Yue Jian, Sibei Ruan, Feng Ling, Mingxi Tang

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in molecular biosciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.4field-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

18 citing papers in PubMed, 17 citations in OpenAlex.

  1. E3 Ubiquitin Ligases in MASH-Associated Liver Fibrosis: Mechanisms and Therapeutic Opportunities.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Review
  2. Ferroptosis in liver biology and diseases.Hepatology communications · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. The role and mechanisms of vitamin A in suppressing hepatic stellate cell activation.Apoptosis : an international journal on programmed cell death · 2026
    Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Article
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.

Rui TangSchool of Basic Medical Sciences, Southwest Medical University, Luzhou, Sichuan, China.
Jing LuoSchool of Basic Medical Sciences, Southwest Medical University, Luzhou, Sichuan, China.
Xiaoxia ZhuDepartment of Pathology, Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.
Pengyu MiaoSchool of Basic Medical Sciences, Southwest Medical University, Luzhou, Sichuan, China.
Hong TangDepartment of Pathology, Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.
Yue JianSchool of Basic Medical Sciences, Southwest Medical University, Luzhou, Sichuan, China.
Sibei RuanDepartment of Pathology, Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.
Feng LingDepartment of Pathology, Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.
Mingxi TangDepartment of Pathology, Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.
Affiliated Hospital of Southwest Medical University · CNSouthwest Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibrosis is a common pathological process that must take place for multiple chronic liver diseases to develop into cirrhosis and liver cancer. Liver fibrosis (LF) is regulated by various cytokines and signaling pathways in its occurrence and development. Ferroptosis is an important mode of cell death caused by iron-dependent oxidative damage and is regulated by iron metabolism and lipid peroxidation signaling pathways. In recent years, numerous studies have shown that ferroptosis is closely related to LF. As the main material secreted by the extracellular matrix, hepatic stellate cells (HSCs) are a general concern in the development of LF. Therefore, targeting HSC ferroptosis against LF is crucial. This review describes the current status of treating LF by inducing HSC ferroptosis that would aid studies in better understanding the current knowledge on ferroptosis in HSCs and the future research direction in this field.

Indexed as

ferroptosisHSCsiron ionslipid peroxidationliver fibrosis

Identifiers

PMID37860583
PMCPMC10584331
OpenAlexW4387098461

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.