Exploring RNA cargo in extracellular vesicles for pleural mesothelioma detection

Abstract Background Pleural Mesothelioma (PM) is a highly aggressive cancer, for which effective early detection remains a challenge due to limited screening options and low sensitivity of biomarkers discovered so far. While extracellular vesicles (EVs) have emerged as promising candidates for blood...

Full description

Saved in:
Bibliographic Details
Main Authors: Agnieszka Kraft, Michaela B. Kirschner, Vanessa Orlowski, Manuel Ronner, Caroline Bodmer, Valentina Boeva, Isabelle Opitz, Mayura Meerang
Format: Article
Language:English
Published: BMC 2025-02-01
Series:BMC Cancer
Subjects:
Online Access:https://doi.org/10.1186/s12885-025-13617-y
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1823861947581333504
author Agnieszka Kraft
Michaela B. Kirschner
Vanessa Orlowski
Manuel Ronner
Caroline Bodmer
Valentina Boeva
Isabelle Opitz
Mayura Meerang
author_facet Agnieszka Kraft
Michaela B. Kirschner
Vanessa Orlowski
Manuel Ronner
Caroline Bodmer
Valentina Boeva
Isabelle Opitz
Mayura Meerang
author_sort Agnieszka Kraft
collection DOAJ
description Abstract Background Pleural Mesothelioma (PM) is a highly aggressive cancer, for which effective early detection remains a challenge due to limited screening options and low sensitivity of biomarkers discovered so far. While extracellular vesicles (EVs) have emerged as promising candidates for blood-based biomarkers, their role in PM has not been studied yet. In this study, we characterized the transcriptomic profile of EVs secreted by PM primary cells and explored their potential as a biomarker source for PM detection. Methods We collected cell culture supernatant from early-passage PM cell cultures derived from the pleural effusion of 4 PM patients. EVs were isolated from the supernatant using Qiagen exoEasy Maxi kit. RNA isolation from EVs was done using the mirVana PARIS kit. Finally, single-end RNA sequencing was done with Illumina Novaseq 6000. Results We identified a range of RNA species expressed in EVs secreted by PM cells, including protein-coding RNA (80%), long non-coding RNA (13%), pseudogenes (4.5%), and short non-coding RNA (1.6%). We detected a subset of genes associated with the previously identified epithelioid (32 genes) and sarcomatoid molecular components (36 genes) in PM-EVs. To investigate whether these markers could serve as biomarkers for PM detection in blood, we compared the RNA content of PM-EVs with the cargo of EVs isolated from the plasma of healthy donors (publicly available data). Majority of upregulated genes in PM-EVs were protein-coding and long non-coding RNAs. Interestingly, 25 of them were the sarcomatoid and epithelioid marker genes. Finally, functional analysis revealed that the PM-EV RNA cargo was associated with Epithelial-Mesenchymal transition, glycolysis, and hypoxia. Conclusions This is the first study to characterize the transcriptomic profile of EVs secreted by PM primary cell cultures, demonstrating their potential as biomarker source for early detection. Further investigation of the functional role of PM-EVs will provide new insights into disease biology and therapeutic avenues.
format Article
id doaj-art-29280558b3d142da85e80d693db7ddb0
institution Kabale University
issn 1471-2407
language English
publishDate 2025-02-01
publisher BMC
record_format Article
series BMC Cancer
spelling doaj-art-29280558b3d142da85e80d693db7ddb02025-02-09T12:41:46ZengBMCBMC Cancer1471-24072025-02-0125111710.1186/s12885-025-13617-yExploring RNA cargo in extracellular vesicles for pleural mesothelioma detectionAgnieszka Kraft0Michaela B. Kirschner1Vanessa Orlowski2Manuel Ronner3Caroline Bodmer4Valentina Boeva5Isabelle Opitz6Mayura Meerang7Department of Thoracic Surgery, University Hospital ZurichDepartment of Thoracic Surgery, University Hospital ZurichDepartment of Thoracic Surgery, University Hospital ZurichDepartment of Thoracic Surgery, University Hospital ZurichDepartment of Thoracic Surgery, University Hospital ZurichInstitute for Machine Learning, Department of Computer Science, ETH ZurichDepartment of Thoracic Surgery, University Hospital ZurichDepartment of Thoracic Surgery, University Hospital ZurichAbstract Background Pleural Mesothelioma (PM) is a highly aggressive cancer, for which effective early detection remains a challenge due to limited screening options and low sensitivity of biomarkers discovered so far. While extracellular vesicles (EVs) have emerged as promising candidates for blood-based biomarkers, their role in PM has not been studied yet. In this study, we characterized the transcriptomic profile of EVs secreted by PM primary cells and explored their potential as a biomarker source for PM detection. Methods We collected cell culture supernatant from early-passage PM cell cultures derived from the pleural effusion of 4 PM patients. EVs were isolated from the supernatant using Qiagen exoEasy Maxi kit. RNA isolation from EVs was done using the mirVana PARIS kit. Finally, single-end RNA sequencing was done with Illumina Novaseq 6000. Results We identified a range of RNA species expressed in EVs secreted by PM cells, including protein-coding RNA (80%), long non-coding RNA (13%), pseudogenes (4.5%), and short non-coding RNA (1.6%). We detected a subset of genes associated with the previously identified epithelioid (32 genes) and sarcomatoid molecular components (36 genes) in PM-EVs. To investigate whether these markers could serve as biomarkers for PM detection in blood, we compared the RNA content of PM-EVs with the cargo of EVs isolated from the plasma of healthy donors (publicly available data). Majority of upregulated genes in PM-EVs were protein-coding and long non-coding RNAs. Interestingly, 25 of them were the sarcomatoid and epithelioid marker genes. Finally, functional analysis revealed that the PM-EV RNA cargo was associated with Epithelial-Mesenchymal transition, glycolysis, and hypoxia. Conclusions This is the first study to characterize the transcriptomic profile of EVs secreted by PM primary cell cultures, demonstrating their potential as biomarker source for early detection. Further investigation of the functional role of PM-EVs will provide new insights into disease biology and therapeutic avenues.https://doi.org/10.1186/s12885-025-13617-yPleural mesotheliomaBiomarkersExtracellular vesiclesTranscriptomicsDiagnosis
spellingShingle Agnieszka Kraft
Michaela B. Kirschner
Vanessa Orlowski
Manuel Ronner
Caroline Bodmer
Valentina Boeva
Isabelle Opitz
Mayura Meerang
Exploring RNA cargo in extracellular vesicles for pleural mesothelioma detection
BMC Cancer
Pleural mesothelioma
Biomarkers
Extracellular vesicles
Transcriptomics
Diagnosis
title Exploring RNA cargo in extracellular vesicles for pleural mesothelioma detection
title_full Exploring RNA cargo in extracellular vesicles for pleural mesothelioma detection
title_fullStr Exploring RNA cargo in extracellular vesicles for pleural mesothelioma detection
title_full_unstemmed Exploring RNA cargo in extracellular vesicles for pleural mesothelioma detection
title_short Exploring RNA cargo in extracellular vesicles for pleural mesothelioma detection
title_sort exploring rna cargo in extracellular vesicles for pleural mesothelioma detection
topic Pleural mesothelioma
Biomarkers
Extracellular vesicles
Transcriptomics
Diagnosis
url https://doi.org/10.1186/s12885-025-13617-y
work_keys_str_mv AT agnieszkakraft exploringrnacargoinextracellularvesiclesforpleuralmesotheliomadetection
AT michaelabkirschner exploringrnacargoinextracellularvesiclesforpleuralmesotheliomadetection
AT vanessaorlowski exploringrnacargoinextracellularvesiclesforpleuralmesotheliomadetection
AT manuelronner exploringrnacargoinextracellularvesiclesforpleuralmesotheliomadetection
AT carolinebodmer exploringrnacargoinextracellularvesiclesforpleuralmesotheliomadetection
AT valentinaboeva exploringrnacargoinextracellularvesiclesforpleuralmesotheliomadetection
AT isabelleopitz exploringrnacargoinextracellularvesiclesforpleuralmesotheliomadetection
AT mayurameerang exploringrnacargoinextracellularvesiclesforpleuralmesotheliomadetection