Evidence map›Paper›PMID 40959429›Full record

ArticleFrontiers in medicine2025

A mitochondrial ferroptosis-related gene signature predicts prognosis and immune landscape in colon cancer.

Hou Wang

Abstract read
In one paragraph

Article in Frontiers in medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

1 citing paper in PubMed.

  1. 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

1 author.

Hou WangDepartment of Endocrinology and Metabolism, Ningbo No. 2 Hospital, Ningbo, Zhejiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Colon cancer is a highly aggressive gastrointestinal malignancy with significant global health implications. Although mitochondrial ferroptosis-related genes have been implicated in colon cancer progression, their prognostic significance remains inadequately understood. Methods: We conducted a comprehensive analysis of the expression patterns and prognostic value of mitochondrial ferroptosis-related genes in patients with colon cancer, utilizing data from the TCGA and GEO databases. A prognostic risk model was established, followed by evaluations of the tumor microenvironment (TME), immune cell infiltration, tumor mutation burden (TMB), and predicted drug sensitivity. P4HA1, recognized as an important mitochondrial ferroptosis-associated gene, was selected for functional characterization using Results: Four key mitochondrial ferroptosis-associated genes-PDSS2, GRSF1, SLC39A8, and P4HA1-were identified. A nomogram combining the risk score and pTNM stage was constructed to predict patient outcomes. Immune microenvironment analysis revealed distinct differences in immune cell infiltration between the high- and low-risk groups. The risk score was significantly correlated with the expression of TME-related genes and immune checkpoint molecules, suggesting a more immunosuppressive microenvironment in high-risk patients. Furthermore, integrating the risk score with TMB enhanced the accuracy of survival prediction. Silencing P4HA1 markedly reduces the proliferative and migratory abilities of colorectal cancer cells Conclusion: This mitochondrial ferroptosis-based risk model represents a promising prognostic biomarker and may offer valuable insights for personalized treatment strategies in colon cancer management. P4HA1 facilitates the advancement of colorectal cancer, while its suppression diminishes the

Indexed as

colon cancerdrug sensitivityimmunotherapymitochondrial ferroptosisprognostic biomarkertumor microenvironment

Identifiers

PMID40959429
PMCPMC12434033

What Socratic holds

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Registered trials

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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.