Evidence map›Paper›PMID 39974379›Full record

ArticleTranslational cancer research2025

Development and validation of a prognostic model based on disulfidptosis-related ferroptosis genes:

Nan Yi, Yuanzi Zhou, Dong Di, Xindong Yin, Xiao Feng, Wenya Xing, Chaoqun Ma, Cunbing Xia

Abstract read
In one paragraph

Article in Translational cancer research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

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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

8 authors.

Nan Yi *Department of General Surgery, Jiangsu Province Hospital of Chinese Medicine, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, China.
Yuanzi Zhou *Department of General Surgery, Jiangsu Province Hospital of Chinese Medicine, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, China.
Dong DiThe First Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, China.
Xindong YinDepartment of General Surgery, Jiangsu Province Hospital of Chinese Medicine, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, China.
Xiao FengDepartment of General Surgery, Jiangsu Province Hospital of Chinese Medicine, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, China.
Wenya XingDepartment of General Surgery, Jiangsu Province Hospital of Chinese Medicine, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, China.
Chaoqun MaDepartment of General Surgery, Jiangsu Province Hospital of Chinese Medicine, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, China.
Cunbing XiaDepartment of General Surgery, Jiangsu Province Hospital of Chinese Medicine, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Disulfidptosis and ferroptosis are emerging cell death modalities crucial to cancer progression, yet their prognostic potential in colon cancer (CC) remains underexplored. This study develops and validates a prognostic model based on Methods: Transcriptomic and clinical data from 476 CC samples and 41 normal colon samples were obtained from The Cancer Genome Atlas (TCGA) database, with 452 patient samples utilized for survival analysis. A training cohort and a validation cohort were generated through random allocation. Disulfidptosis-related ferroptosis genes (DRFGs) were identified using Pearson correlation analysis, and a prognostic model was built using the least absolute shrinkage and selection operator (LASSO) and Cox regression analysis. External validation was performed using the Gene Expression Omnibus (GEO) datasets (GSE17538 and GSE38832), and clinical samples were further analyzed through immunohistochemistry. Predictors in the nomogram included age, gender, tumor stage, and risk score. The C-index of the final model was used to assess its prognostic accuracy. Results: The results were validated using external cohorts from the GEO database and immunohistochemistry experiments. A prognostic model incorporating Conclusions: This DRFG-based prognostic model offers an effective tool for predicting clinical outcomes in CC and can guide personalized treatment strategies. The upregulation of

Indexed as

Colon cancer (CC)disulfidptosisferroptosisprognostic model

Identifiers

PMID39974379
PMCPMC11833425

What Socratic holds

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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.