Are circulating microRNAs suitable for the early detection of malignant mesothelioma? Results from a nested

Daniel Gilbert Weber1, Alexander Brik2, Swaantje Casjens2

  • 1Institute for Prevention and Occupational Medicine of the German Social Accident Insurance, Institute of the Ruhr University Bochum (IPA), Buerkle-de-la-Camp-Platz 1, 44789, Bochum, Germany. weber@ipa-dguv.de.

BMC Research Notes
|February 13, 2019
PubMed
Abstract

Insights

Investigating circulating microRNAs (miRNAs) like miR-132-3p, miR-126-3p, and miR-103a-3p for early malignant mesothelioma detection proved unsuccessful. These biomarkers did not show efficacy in prediagnostic plasma samples.

Area of Science:

  • Oncology
  • Molecular Biology
  • Biomarker Discovery

Background:

  • Malignant mesothelioma is an aggressive cancer requiring early detection methods.
  • Non- or minimally-invasive biomarkers are crucial for identifying mesothelioma at earlier stages.
  • Specific circulating microRNAs (miRNAs) have been investigated as potential diagnostic markers.

Purpose of the Study:

  • To evaluate the diagnostic potential of circulating miR-132-3p, miR-126-3p, and miR-103a-3p for early detection of malignant mesothelioma.
  • To assess the feasibility of these miRNAs as prediagnostic biomarkers in plasma samples.

Main Methods:

  • A nested case-control study design was employed.
  • Plasma samples from 17 prediagnostic malignant mesothelioma cases and 34 matched asbestos-exposed controls were analyzed.
  • Levels of miR-132-3p, miR-126-3p, and miR-103a-3p were quantified in prediagnostic samples.

Main Results:

  • The analyzed miRNAs (miR-132-3p, miR-126-3p, and miR-103a-3p) demonstrated 0% sensitivity at a specificity of 98%.
  • These miRNAs failed to detect malignant mesothelioma in prediagnostic plasma samples collected a median of 8.9 months prior to diagnosis.
  • The study indicates these miRNAs are not feasible for the early detection of malignant mesothelioma.

Conclusions:

  • Circulating miR-132-3p, miR-126-3p, and miR-103a-3p are not suitable biomarkers for the early detection of malignant mesothelioma.
  • Further research is warranted to explore the potential of these miRNAs as prognostic or predictive markers for therapy response.
  • Future studies should focus on different patient cohorts and experimental designs to validate potential roles beyond early diagnosis.

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