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Diagnostic Potential of Exosomal microRNAs in Colorectal Cancer

Background: Despite the significance of colonoscopy for early diagnosis of colorectal adenocarcinoma (CRC), population-wide screening remains challenging, mainly because of low acceptance rates. Herein, exosomal (exo-miR) and free circulating microRNA (c-miR) may be used as liquid biopsies in CRC to...

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Autores principales: Dohmen, Jonas, Semaan, Alexander, Kobilay, Makbule, Zaleski, Martin, Branchi, Vittorio, Schlierf, Anja, Hettwer, Karina, Uhlig, Steffen, Hartmann, Gunther, Kalff, Jörg C., Matthaei, Hanno, Lingohr, Philipp, Holdenrieder, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9221658/
https://www.ncbi.nlm.nih.gov/pubmed/35741223
http://dx.doi.org/10.3390/diagnostics12061413
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author Dohmen, Jonas
Semaan, Alexander
Kobilay, Makbule
Zaleski, Martin
Branchi, Vittorio
Schlierf, Anja
Hettwer, Karina
Uhlig, Steffen
Hartmann, Gunther
Kalff, Jörg C.
Matthaei, Hanno
Lingohr, Philipp
Holdenrieder, Stefan
author_facet Dohmen, Jonas
Semaan, Alexander
Kobilay, Makbule
Zaleski, Martin
Branchi, Vittorio
Schlierf, Anja
Hettwer, Karina
Uhlig, Steffen
Hartmann, Gunther
Kalff, Jörg C.
Matthaei, Hanno
Lingohr, Philipp
Holdenrieder, Stefan
author_sort Dohmen, Jonas
collection PubMed
description Background: Despite the significance of colonoscopy for early diagnosis of colorectal adenocarcinoma (CRC), population-wide screening remains challenging, mainly because of low acceptance rates. Herein, exosomal (exo-miR) and free circulating microRNA (c-miR) may be used as liquid biopsies in CRC to identify individuals at risk. Direct comparison of both compartments has shown inconclusive results, which is why we directly compared a panel of 10 microRNAs in this entity. Methods: Exo-miR and c-miR levels were measured using real-time quantitative PCR after isolation from serum specimens in a cohort of 69 patients. Furthermore, results were compared to established tumor markers CEA and CA 19-9. Results: Direct comparison of exo- and c-miR biopsy results showed significantly higher microRNA levels in the exosomal compartment (p < 0.001). Exo-Let7, exo-miR-16 and exo-miR-23 significantly differed between CRC and healthy controls (all p < 0.05), while no c-miR showed this potential. Sensitivity and specificity can be further enhanced using combinations of multiple exosomal miRNAs. Conclusions: Exosomal microRNA should be considered as a promising biomarker in CRC for future studies. Nonetheless, results may show interference with common comorbidities, which must be taken into account in future studies.
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spelling pubmed-92216582022-06-24 Diagnostic Potential of Exosomal microRNAs in Colorectal Cancer Dohmen, Jonas Semaan, Alexander Kobilay, Makbule Zaleski, Martin Branchi, Vittorio Schlierf, Anja Hettwer, Karina Uhlig, Steffen Hartmann, Gunther Kalff, Jörg C. Matthaei, Hanno Lingohr, Philipp Holdenrieder, Stefan Diagnostics (Basel) Article Background: Despite the significance of colonoscopy for early diagnosis of colorectal adenocarcinoma (CRC), population-wide screening remains challenging, mainly because of low acceptance rates. Herein, exosomal (exo-miR) and free circulating microRNA (c-miR) may be used as liquid biopsies in CRC to identify individuals at risk. Direct comparison of both compartments has shown inconclusive results, which is why we directly compared a panel of 10 microRNAs in this entity. Methods: Exo-miR and c-miR levels were measured using real-time quantitative PCR after isolation from serum specimens in a cohort of 69 patients. Furthermore, results were compared to established tumor markers CEA and CA 19-9. Results: Direct comparison of exo- and c-miR biopsy results showed significantly higher microRNA levels in the exosomal compartment (p < 0.001). Exo-Let7, exo-miR-16 and exo-miR-23 significantly differed between CRC and healthy controls (all p < 0.05), while no c-miR showed this potential. Sensitivity and specificity can be further enhanced using combinations of multiple exosomal miRNAs. Conclusions: Exosomal microRNA should be considered as a promising biomarker in CRC for future studies. Nonetheless, results may show interference with common comorbidities, which must be taken into account in future studies. MDPI 2022-06-08 /pmc/articles/PMC9221658/ /pubmed/35741223 http://dx.doi.org/10.3390/diagnostics12061413 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Dohmen, Jonas
Semaan, Alexander
Kobilay, Makbule
Zaleski, Martin
Branchi, Vittorio
Schlierf, Anja
Hettwer, Karina
Uhlig, Steffen
Hartmann, Gunther
Kalff, Jörg C.
Matthaei, Hanno
Lingohr, Philipp
Holdenrieder, Stefan
Diagnostic Potential of Exosomal microRNAs in Colorectal Cancer
title Diagnostic Potential of Exosomal microRNAs in Colorectal Cancer
title_full Diagnostic Potential of Exosomal microRNAs in Colorectal Cancer
title_fullStr Diagnostic Potential of Exosomal microRNAs in Colorectal Cancer
title_full_unstemmed Diagnostic Potential of Exosomal microRNAs in Colorectal Cancer
title_short Diagnostic Potential of Exosomal microRNAs in Colorectal Cancer
title_sort diagnostic potential of exosomal micrornas in colorectal cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9221658/
https://www.ncbi.nlm.nih.gov/pubmed/35741223
http://dx.doi.org/10.3390/diagnostics12061413
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