Gastrointestinal Disorders (Aug 2022)

Identification of a Five-MiRNA Expression Assay to Aid Colorectal Cancer Diagnosis

  • Matthew G. Davey,
  • Gerard Feeney,
  • Heidi Annuk,
  • Maxwell Paganga,
  • Emma Holian,
  • Aoife J. Lowery,
  • Michael J. Kerin,
  • Nicola Miller

DOI
https://doi.org/10.3390/gidisord4030018
Journal volume & issue
Vol. 4, no. 3
pp. 190 – 204

Abstract

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Introduction: One-third of colorectal cancer (CRC) patients present with advanced disease, and establishing control remains a challenge. Identifying novel biomarkers to facilitate earlier diagnosis is imperative in enhancing oncological outcomes. We aimed to create miRNA oncogenic signature to aid CRC diagnosis. Methods: Tumour and tumour-associated normal (TAN) were extracted from 74 patients during surgery for CRC. RNA was isolated and target miRNAs were quantified using real-time reverse transcriptase polymerase chain reaction. Regression analyses were performed in order to identify miRNA targets capable of differentiating CRC from TAN and compared with two endogenous controls (miR-16 and miR-345) in each sample. Areas under the curve (AUCs) in Receiver Operating Characteristic (ROC) analyses were determined. Results: MiR-21 (β-coefficient:3.661, SE:1.720, p = 0.033), miR-31 (β-coefficient:2.783, SE:0.918, p = 0.002), and miR-150 (β-coefficient:−4.404, SE:0.526, p = 0.004) expression profiles differentiated CRC from TAN. In multivariable analyses, increased miR-31 (β-coefficient:2.431, SE:0.715, p p p p = 0.001), miR-31 (p = 0.001), and miR-150 (p p = 0.476), miR-31 (p = 0.933), and miR-150 (p = 0.148) failed to differentiate these groups. Conclusion: This study identified a five-miRNA signature capable of distinguishing CRC from normal tissues with a high diagnostic test accuracy. Further experimentation with this signature is required to elucidate its diagnostic relevance in the circulation of CRC patients.

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