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A novel microRNA signature for the detection of melanoma by liquid biopsy
BACKGROUND: Melanoma is the deadliest form of skin cancer and metastatic disease is associated with a significant survival rate drop. There is an urgent need for consistent tumor biomarkers to scale precision medicine and reduce cancer mortality. Here, we aimed to identify a melanoma-specific circul...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9571479/ https://www.ncbi.nlm.nih.gov/pubmed/36243798 http://dx.doi.org/10.1186/s12967-022-03668-1 |
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author | Sabato, Claudia Noviello, Teresa Maria Rosaria Covre, Alessia Coral, Sandra Caruso, Francesca Pia Besharat, Zein Mersini Splendiani, Elena Masuelli, Laura Battistelli, Cecilia Vacca, Alessandra Catanzaro, Giuseppina Po, Agnese Anichini, Andrea Maio, Michele Ceccarelli, Michele Di Giacomo, Anna Maria Ferretti, Elisabetta |
author_facet | Sabato, Claudia Noviello, Teresa Maria Rosaria Covre, Alessia Coral, Sandra Caruso, Francesca Pia Besharat, Zein Mersini Splendiani, Elena Masuelli, Laura Battistelli, Cecilia Vacca, Alessandra Catanzaro, Giuseppina Po, Agnese Anichini, Andrea Maio, Michele Ceccarelli, Michele Di Giacomo, Anna Maria Ferretti, Elisabetta |
author_sort | Sabato, Claudia |
collection | PubMed |
description | BACKGROUND: Melanoma is the deadliest form of skin cancer and metastatic disease is associated with a significant survival rate drop. There is an urgent need for consistent tumor biomarkers to scale precision medicine and reduce cancer mortality. Here, we aimed to identify a melanoma-specific circulating microRNA signature and assess its value as a diagnostic tool. METHODS: The study consisted of a discovery phase and two validation phases. Circulating plasma extracellular vesicles (pEV) associated microRNA profiles were obtained from a discovery cohort of metastatic melanoma patients and normal subjects as controls. A pEV-microRNA signature was obtained using a LASSO penalized logistic regression model. The pEV-microRNA signature was subsequently validated both in a publicly available dataset and in an independent internal cohort. RESULTS: We identified and validated in three independent cohorts a panel of melanoma-specific circulating microRNAs that showed high accuracy in differentiating melanoma patients from healthy subjects with an area under the curve (AUC) of 1.00, 0.94 and 0.75 respectively. Investigation of the function of the pEV-microRNA signature evidenced their possible immune suppressive role in melanoma patients. CONCLUSIONS: We demonstrate that a blood test based on circulating microRNAs can non-invasively detect melanoma, offering a novel diagnostic tool for improving standard care. Moreover, we revealed an immune suppressive role for melanoma pEV-microRNAs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12967-022-03668-1. |
format | Online Article Text |
id | pubmed-9571479 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-95714792022-10-17 A novel microRNA signature for the detection of melanoma by liquid biopsy Sabato, Claudia Noviello, Teresa Maria Rosaria Covre, Alessia Coral, Sandra Caruso, Francesca Pia Besharat, Zein Mersini Splendiani, Elena Masuelli, Laura Battistelli, Cecilia Vacca, Alessandra Catanzaro, Giuseppina Po, Agnese Anichini, Andrea Maio, Michele Ceccarelli, Michele Di Giacomo, Anna Maria Ferretti, Elisabetta J Transl Med Research BACKGROUND: Melanoma is the deadliest form of skin cancer and metastatic disease is associated with a significant survival rate drop. There is an urgent need for consistent tumor biomarkers to scale precision medicine and reduce cancer mortality. Here, we aimed to identify a melanoma-specific circulating microRNA signature and assess its value as a diagnostic tool. METHODS: The study consisted of a discovery phase and two validation phases. Circulating plasma extracellular vesicles (pEV) associated microRNA profiles were obtained from a discovery cohort of metastatic melanoma patients and normal subjects as controls. A pEV-microRNA signature was obtained using a LASSO penalized logistic regression model. The pEV-microRNA signature was subsequently validated both in a publicly available dataset and in an independent internal cohort. RESULTS: We identified and validated in three independent cohorts a panel of melanoma-specific circulating microRNAs that showed high accuracy in differentiating melanoma patients from healthy subjects with an area under the curve (AUC) of 1.00, 0.94 and 0.75 respectively. Investigation of the function of the pEV-microRNA signature evidenced their possible immune suppressive role in melanoma patients. CONCLUSIONS: We demonstrate that a blood test based on circulating microRNAs can non-invasively detect melanoma, offering a novel diagnostic tool for improving standard care. Moreover, we revealed an immune suppressive role for melanoma pEV-microRNAs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12967-022-03668-1. BioMed Central 2022-10-15 /pmc/articles/PMC9571479/ /pubmed/36243798 http://dx.doi.org/10.1186/s12967-022-03668-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Sabato, Claudia Noviello, Teresa Maria Rosaria Covre, Alessia Coral, Sandra Caruso, Francesca Pia Besharat, Zein Mersini Splendiani, Elena Masuelli, Laura Battistelli, Cecilia Vacca, Alessandra Catanzaro, Giuseppina Po, Agnese Anichini, Andrea Maio, Michele Ceccarelli, Michele Di Giacomo, Anna Maria Ferretti, Elisabetta A novel microRNA signature for the detection of melanoma by liquid biopsy |
title | A novel microRNA signature for the detection of melanoma by liquid biopsy |
title_full | A novel microRNA signature for the detection of melanoma by liquid biopsy |
title_fullStr | A novel microRNA signature for the detection of melanoma by liquid biopsy |
title_full_unstemmed | A novel microRNA signature for the detection of melanoma by liquid biopsy |
title_short | A novel microRNA signature for the detection of melanoma by liquid biopsy |
title_sort | novel microrna signature for the detection of melanoma by liquid biopsy |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9571479/ https://www.ncbi.nlm.nih.gov/pubmed/36243798 http://dx.doi.org/10.1186/s12967-022-03668-1 |
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