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pmid:38542291

Unveiling Prognostic RNA Biomarkers through a Multi-Cohort Study in Colorectal Cancer.

Zehwan Kim · Jaebon Lee · Ye Eun Yoon · Jae Won Yun

International journal of molecular sciences · 2024 doi:10.3390/ijms25063317

Paper

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Experiment

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Data

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Analysis

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Execution

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title
Unveiling Prognostic RNA Biomarkers through a Multi-Cohort Study in Colorectal Cancer.
doi
10.3390/ijms25063317
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38542291
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Zehwan Kim
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Jaebon Lee
[2]
Ye Eun Yoon
[3]
Jae Won Yun
journal
International journal of molecular sciences
year
2024
abstract
Because cancer is a leading cause of death and is thought to be caused by genetic errors or genomic instability in many circumstances, there have been studies exploring cancer's genetic basis using microarray and RNA-seq methods, linking gene expression data to patient survival. This research introduces a methodological framework, combining heterogeneous gene expression data, random forest selection, and pathway analysis, alongside clinical information and Cox regression analysis, to discover prognostic biomarkers. Heterogeneous gene expression data for colorectal cancer were collected from TCGA-COAD (RNA-seq), and GSE17536 and GSE39582 (microarray), and were integrated with Entrez Gene IDs. Using Cox regression analysis and random forest, genes with consistent hazard ratios and significantly affecting patient survivability were chosen. Predictive accuracy was evaluated using ROC curves. Pathway analysis identified potential RNA biomarkers. The authors identified 28 RNA biomarkers. Pathway analysis revealed enrichment in cancer-related pathways, notably EGFR downstream signaling and IGF1R signaling. Three RNA biomarkers (ZEB1-AS1, PI4K2A, and ITGB8-AS1) and two clinical biomarkers (stage and age) were chosen for a prognostic model, improving predictive performance compared to using clinical biomarkers alone. Despite biomarker identification challenges, this study underscores integration of heterogenous gene expression data for discovery.
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Utilizing a multiple Cox regression model that accounted for factors such as age, sex, and tumor stage, 28 RNA biomarkers were identified by filtering for those with significant p-values and consistent hazard ratio direction (HR > 1 in all cohorts or HR < 1 in all cohorts) across the three cohorts (Table 2).
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sections[4] "2.2. Cox Regression Analysis Test Result" paragraph 2
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Utilizing a multiple Cox regression model that accounted for factors such as age, sex, and tumor stage, 28 RNA biomarkers were identified by filtering for those with significant p-values and consistent hazard ratio direction (HR > 1 in all cohorts or HR < 1 in all cohorts) across the three cohorts (Table 2).
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The RNA expression data and clinical data are available in the GEO under the accession number GSE17536 and GSE39582 and in the UCSC XENA website (https://xena.ucsc.edu/, accessed on 6 January 2024).
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The authors identified 28 RNA biomarkers.
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Homo sapiens
title
Gene expression Classification of Colon Cancer defines six molecular subtypes with distinct clinical, molecular and survival characteristics [Expression]
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2026-11-01T15:39:54Z
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Utilizing a multiple Cox regression model that accounted for factors such as age, sex, and tumor stage, 28 RNA biomarkers were identified by filtering for those with significant p-values and consistent hazard ratio direction (HR > 1 in all cohorts or HR < 1 in all cohorts) across the three cohorts (Table 2).
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The RNA expression data and clinical data are available in the GEO under the accession number GSE17536 and GSE39582 and in the UCSC XENA website (https://xena.ucsc.edu/, accessed on 6 January 2024).
basis
The paper names GSE17536, GSE39582 in NCBI GEO and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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Utilizing a multiple Cox regression model that accounted for factors such as age, sex, and tumor stage, 28 RNA biomarkers were identified by filtering for those with significant p-values and consistent hazard ratio direction (HR > 1 in all cohorts or HR < 1 in all cohorts) across the three cohorts (Table 2).
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:38542291", "kind": "science-record", "revision": 3, "content_hash": "sha256:faef9a8e601b981dcf7731bddce2b3bf166bc4689a51417e1056ec14ed33ee73", "created_at": "2026-11-01T19:20:29Z", "updated_at": "2026-11-01T22:11:32Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Unveiling Prognostic RNA Biomarkers through a Multi-Cohort Study in Colorectal Cancer.", "doi": "10.3390/ijms25063317", "pmid": "38542291", "authors": ["Zehwan Kim", "Jaebon Lee", "Ye Eun Yoon", "Jae Won Yun"], "journal": "International journal of molecular sciences", "year": 2024, "abstract": "Because cancer is a leading cause of death and is thought to be caused by genetic errors or genomic instability in many circumstances, there have been studies exploring cancer's genetic basis using microarray and RNA-seq methods, linking gene expression data to patient survival. This research introduces a methodological framework, combining heterogeneous gene expression data, random forest selection, and pathway analysis, alongside clinical information and Cox regression analysis, to discover prognostic biomarkers. Heterogeneous gene expression data for colorectal cancer were collected from TCGA-COAD (RNA-seq), and GSE17536 and GSE39582 (microarray), and were integrated with Entrez Gene IDs. Using Cox regression analysis and random forest, genes with consistent hazard ratios and significantly affecting patient survivability were chosen. Predictive accuracy was evaluated using ROC curves. Pathway analysis identified potential RNA biomarkers. The authors identified 28 RNA biomarkers. Pathway analysis revealed enrichment in cancer-related pathways, notably EGFR downstream signaling and IGF1R signaling. 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