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August 3, 20250 citations

Bioinformatic Screen with Clinical Validation for the Identification of Novel Stool Based mRNA Biomarkers for the Detection of Colorectal Lesions Including Advanced Precancerous Lesions

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HLHoucong LiuLHLoren HansenCSChangpu Song

Key Points

  • The study identifies mRNA biomarkers for colorectal cancer and advanced precancerous lesions based on expression profiles.
  • Top 20 mRNA genes were analyzed in 113 clinical samples, revealing significant differential expression in 14 genes.
  • The combined AUC for CRC detection using clinical stool samples was 0.94, indicating high diagnostic performance.
  • Utilizing existing public datasets can streamline the identification process for clinically relevant mRNA biomarkers.

Abstract

Abstract Messenger RNA (mRNA) stool based biomarkers represent a promising approach for the diagnosis of colorectal cancer (CRC) and advanced precancerous lesions (AA). But it is unclear which mRNA biomarkers have the most clinical utility. This study aims to partially fill this gap by performing an analysis which first ranks genes based on their expression profile in RNA-seq tissue datasets. The diagnostic performance of the top 20 ranked genes was then tested using 113 clinical samples (CRC N=33, AA N=28, Controls N=53). Fourteen of the genes had significant differential expression in the stool of CRC patients compared to controls (false discovery rate or FDR < 0.05). The Pearson correlation coefficient between tissue and stool expression was 0.57 (p-value = 0.007). The combined performance of the 20 genes in clinical stool samples had an area under the receiver operator curve (AUC) of 0.94 for CRC detection (sensitivity 75.5%, specificity 95%) and an AUC of 0.83 (sensitivity 55.8%, specificity 92.6%) for AA detection. The ability to use existing public transcriptomic datasets to identify promising candidate genes can substantially reduce the cost and effort required to screen for clinically useful mRNA biomarkers.

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Cite This Study

Liu et al. (2025) studied this question.

synapsesocial.com/papers/689a0c7be6551bb0af8d076dhttps://doi.org/10.1101/2025.07.16.25331674
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