Circulating microRNAs as biomarkers for risk assessment and prognostic stratification of pleural mesothelioma

Evgeniya Sharova1, Paola Del Bianco2, Loredana Urso1

  • 1Immunology and Molecular Oncology Diagnostics, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy.

PubMed
Abstract

Insights

Circulating microRNAs (miRNAs) show promise as non-invasive biomarkers for detecting pleural mesothelioma (PM) and assessing patient risk. These miRNA signatures can aid in early diagnosis and personalized treatment strategies.

Area of Science:

  • Oncology
  • Molecular Biology
  • Biomarker Discovery

Background:

  • Pleural mesothelioma (PM) is an aggressive cancer linked to asbestos exposure.
  • Current diagnostic and prognostic tools for PM are limited, posing clinical challenges.
  • Minimally invasive biomarkers are needed for early detection and risk stratification.

Purpose of the Study:

  • To evaluate circulating microRNAs (miRNAs) as potential non-invasive biomarkers for pleural mesothelioma (PM).
  • To assess the utility of plasma miRNA signatures for early PM detection.
  • To determine if circulating miRNAs can stratify PM patients based on prognosis.

Main Methods:

  • Plasma samples were collected from 56 PM patients and 32 asbestos-exposed controls.
  • Quantitative RT-PCR was used to screen 92 miRNAs in a discovery cohort.
  • Candidate miRNAs were validated in the full cohort to identify diagnostic and prognostic signatures.

Main Results:

  • Specific plasma miRNA ratios (miR-24-3p, miR-146a-5p, miR-191-5p, miR-200a-3p, miR-222-3p, miR-223-3p, miR-1260a) accurately differentiated PM patients from controls.
  • Circulating miRNA ratios (miR-146a-5p, miR-200a-3p, miR-222-3p, miR-191-5p) stratified epithelioid PM into high- and low-risk groups.
  • High accuracy and sensitivity were achieved in detecting PM and stratifying risk.

Conclusions:

  • Circulating miRNA signatures are promising non-invasive biomarkers for early PM detection.
  • These miRNA profiles can aid in prognostic stratification, especially for epithelioid PM.
  • Integrating these biomarkers into clinical practice may enable personalized treatment and optimize surgical patient selection.