Evidence map›Paper›PMID 41669255›Full record

ArticleFrontiers in oncology2025

Identification of unique biomarkers in colorectal cancer based on comprehensive analysis and machine learning.

Liwei Wang, Aigang Ren, Xiaolong Cui, Yuan Shen, Qingxing Huang

Abstract read
In one paragraph

Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Liwei Wang *Department of Colorectal and Anorectal Surgery, First Hospital of Shanxi Medical University, Taiyuan, China.
Aigang Ren *Department of Colorectal and Anorectal Surgery, First Hospital of Shanxi Medical University, Taiyuan, China.
Xiaolong CuiDepartment of Colorectal and Anorectal Surgery, First Hospital of Shanxi Medical University, Taiyuan, China.
Yuan ShenDepartment of Colorectal and Anorectal Surgery, First Hospital of Shanxi Medical University, Taiyuan, China.
Qingxing HuangDepartment of Colorectal and Anorectal Surgery, First Hospital of Shanxi Medical University, Taiyuan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Colorectal cancer (CRC) is a common malignant tumor with high incidence and poor prognosis. Identifying effective biomarkers is crucial for its diagnosis and treatment. Methods: Gene expression data were obtained from TCGA-CRC and GSE39582 datasets. After preprocessing, differentially expressed genes (DEGs) were screened using the limma package. Hub genes were identified via WGCNA, miRNA-hub/TF-hub gene network construction, and LASSO, SVM-RFE, and random forest algorithms. Subtype analysis, survival analysis, external validation, qRT-PCR, Western blot, and ferroptosis-related assays were performed. Results: Fourteen ferroptosis-mitochondria-RBP-related genes (IMRBPs) were identified, including seven hub RBP genes (APEX1, BRCA1, DNMT1, EZH2, PTTG1, SND1, UHRF1). APEX1 was downregulated in CRC, while the other six were upregulated. The diagnostic model based on these seven genes showed high AUC values (0.818-0.924) in multiple datasets. These hub genes were associated with ferroptosis suppression by regulating GSH/GSSGand Fe²⁺ levels. Discussion: The seven hub RBP genes are potential biomarkers for CRC, providing new insights and therapeutic targets. However, functional validation and larger sample sizes are needed for clinical application.

Indexed as

bioinformatics analysisbiomarkerscolorectal cancerferroptosismachine learning

Identifiers

PMID41669255
PMCPMC12883654

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