Evidence map›Paper›PMID 42584759›Full record

ReviewCell biochemistry and biophysics2026

Ferroptosis-Inflammation Crosstalk: Mechanistic Insights and Emerging Drug Targets.

Sanjivani Gupta, Sayali Mukherjee

Abstract readReview
PubMed Publisher
In one paragraph

Review in Cell biochemistry and biophysics, 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

2 authors.

Sanjivani GuptaAmity Institute of Biotechnology, Amity University Uttar Pradesh, Lucknow Campus, Lucknow, Uttar Pradesh, India.
Sayali MukherjeeAmity Institute of Biotechnology, Amity University Uttar Pradesh, Lucknow Campus, Lucknow, Uttar Pradesh, India. smukherjee@lko.amity.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ferroptosis, a non-apoptotic form of regulated cell death characterized by iron accumulation and lipid peroxidation, has recently established its crucial role in inflammation and immune - related diseases. The current review aims at offering a comprehensive synthesis of the Interaction between ferroptosis and inflammation that governs the ferroptosis-inflammation axis, in which the inflammation environment and cell death process operates that can influence each other through difficult molecular pathways. In this context, this article discusses how inflammatory signalling pathways works, in terms of the inflammation environment, as exemplified by the pathway of the IFN-γ JAK/STAT1 axis, that regulates the ferroptotic pathway by inhibiting system Xc

Indexed as

FerroptosisInflammationAnimalsAntioxidantsHumansInflammasomesIronIron Chelating AgentsLipid PeroxidationSignal TransductionAntioxidantsInflammasomesIronIron Chelating AgentsCytokinesDrug targetsFerroptosisInflammationIron overloadLipid peroxidation

Identifiers

PMID42584759

What Socratic 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 Socratic graph.