Evidence map›Paper›PMID 41898725›Full record

ReviewInternational journal of molecular sciences2026

The Mechanism of G Protein-Coupled Receptor Regulation of Ferroptosis in Hepatic Ischemia-Reperfusion Injury.

Die Hu, Lei Sun, Mei Su, Xuekun Xing

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Die HuSchool of Public Health, Guilin Medical University, Guilin 541199, China.
Lei SunSchool of Public Health, Guilin Medical University, Guilin 541199, China.ORCID 0009-0002-7643-4609
Mei SuSchool of Public Health, Guilin Medical University, Guilin 541199, China.
Xuekun XingSchool of Public Health, Guilin Medical University, Guilin 541199, China.

Funding

Guangxi Natural Science Foundation 2025JJA141021National Natural Science Foundation of China 82260802
6 · The paper itself

Abstract

Hepatic ischemia-reperfusion injury (HIRI) is a significant clinical challenge in the field of liver surgery and transplantation, and its pathological mechanisms are complex. In recent years, ferroptosis, a novel form of iron-dependent programmed cell death, plays a central role in this injury process. G protein-coupled receptors (GPCRs), as the largest family of membrane receptors in the body, regulate cellular stress and death through extensive signaling networks. This review elucidates the specific molecular mechanisms by which GPCRs regulate ferroptosis in HIRI by affecting key pathways such as lipid peroxidation, iron metabolism homeostasis, and antioxidant defense. It further explores potential therapeutic strategies targeting specific GPCRs to modulate ferroptosis, thereby alleviating liver injury and improving postoperative outcomes, to provide new insights and a theoretical basis for clinical translation.

Indexed as

FerroptosisLiverLiver DiseasesReceptors, G-Protein-CoupledReperfusion InjuryAnimalsHumansIronLipid PeroxidationSignal TransductionIronReceptors, G-Protein-CoupledferroptosisG protein-coupled receptorhepatic ischemia–reperfusion injuryiron metabolismlipid peroxidation

Identifiers

PMID41898725
PMCPMC13027305

What Socratic 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 Socratic graph.