Evidence map›Paper›PMID 41427530›Full record

ArticleInternational journal of surgery (London, England)2026

Ferroptosis in renal cell carcinoma: integrative multi-omics insights and therapeutic perspectives.

Xing Wang, Jun Li, Yunfeng Zhang, Ruizhen Huang, Penglin Zhang, Honglin Hu

Abstract read
In one paragraph

Article in International journal of surgery (London, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Oncology research · 2026
    Article
  3. Review
  4. Review
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.

Xing WangDepartment of Urology, The Second Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, China.ORCID 0000-0001-5638-518
Jun Li
Yunfeng Zhang
Ruizhen Huang
Penglin Zhang
Honglin Hu

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renal cell carcinoma (RCC) exhibits marked heterogeneity in its molecular landscape and clinical behavior. Ferroptosis, an iron-dependent and lipid peroxidation-driven form of cell death, has emerged as a biologically relevant process in RCC pathogenesis. This review summarizes recent advances in the multi-omics dissection of ferroptosis in RCC, including findings from genomics, epigenomics, transcriptomics, proteomics, metabolomics, and microbiomics. Key molecular regulators such as VHL, SLC7A11, GPX4, and ACSL4 are highlighted for their roles in ferroptosis sensitivity or resistance. In parallel, insights from single-cell and spatial omics offer new perspectives on cell-type specificity and microenvironmental context. We also discuss the implications of ferroptosis in therapeutic modulation, including potential integration with immune checkpoint inhibitors and metabolic interventions. This review aims to provide a coherent overview of ferroptosis in RCC and inform future mechanistic studies and translational strategies.

Indexed as

ferroptosisglutathione peroxidase 4 (GPX4)multi-omics integrationrenal cell carcinoma (RCC)tumor microenvironment

Identifiers

PMID41427530
PMCPMC13105629

What OpenQuestion holds

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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.