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Tumor-associated factors are enriched in lymphatic exudate compared to plasma in metastatic melanoma patients
Liquid biopsies allow monitoring of cancer progression and detection of relapse, but reliable biomarkers in melanoma are lacking. Because secreted factors preferentially drain to lymphatic vessels before dilution in the blood, we hypothesized that lymph should be vastly enriched in cancer biomarkers...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6504224/ https://www.ncbi.nlm.nih.gov/pubmed/30975896 http://dx.doi.org/10.1084/jem.20181618 |
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author | Broggi, Maria A.S. Maillat, Lea Clement, Cristina C. Bordry, Natacha Corthésy, Patricia Auger, Aymeric Matter, Maurice Hamelin, Romain Potin, Lambert Demurtas, Davide Romano, Emanuela Harari, Alexandre Speiser, Daniel E. Santambrogio, Laura Swartz, Melody A. |
author_facet | Broggi, Maria A.S. Maillat, Lea Clement, Cristina C. Bordry, Natacha Corthésy, Patricia Auger, Aymeric Matter, Maurice Hamelin, Romain Potin, Lambert Demurtas, Davide Romano, Emanuela Harari, Alexandre Speiser, Daniel E. Santambrogio, Laura Swartz, Melody A. |
author_sort | Broggi, Maria A.S. |
collection | PubMed |
description | Liquid biopsies allow monitoring of cancer progression and detection of relapse, but reliable biomarkers in melanoma are lacking. Because secreted factors preferentially drain to lymphatic vessels before dilution in the blood, we hypothesized that lymph should be vastly enriched in cancer biomarkers. We characterized postoperative lymphatic exudate and plasma of metastatic melanoma patients after lymphadenectomy and found a dramatic enrichment in lymphatic exudate of tumor-derived factors and especially extracellular vesicles containing melanoma-associated proteins and miRNAs, with unique protein signatures reflecting early versus advanced metastatic spread. Furthermore, lymphatic exudate was enriched in memory T cells, including tumor-reactive CD137(+) and stem cell–like types. In mice, lymph vessels were the major route of extracellular vesicle transport from tumors to the systemic circulation. We suggest that lymphatic exudate provides a rich source of tumor-derived factors for enabling the discovery of novel biomarkers that may reflect disease stage and therapeutic response. |
format | Online Article Text |
id | pubmed-6504224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-65042242019-11-06 Tumor-associated factors are enriched in lymphatic exudate compared to plasma in metastatic melanoma patients Broggi, Maria A.S. Maillat, Lea Clement, Cristina C. Bordry, Natacha Corthésy, Patricia Auger, Aymeric Matter, Maurice Hamelin, Romain Potin, Lambert Demurtas, Davide Romano, Emanuela Harari, Alexandre Speiser, Daniel E. Santambrogio, Laura Swartz, Melody A. J Exp Med Research Articles Liquid biopsies allow monitoring of cancer progression and detection of relapse, but reliable biomarkers in melanoma are lacking. Because secreted factors preferentially drain to lymphatic vessels before dilution in the blood, we hypothesized that lymph should be vastly enriched in cancer biomarkers. We characterized postoperative lymphatic exudate and plasma of metastatic melanoma patients after lymphadenectomy and found a dramatic enrichment in lymphatic exudate of tumor-derived factors and especially extracellular vesicles containing melanoma-associated proteins and miRNAs, with unique protein signatures reflecting early versus advanced metastatic spread. Furthermore, lymphatic exudate was enriched in memory T cells, including tumor-reactive CD137(+) and stem cell–like types. In mice, lymph vessels were the major route of extracellular vesicle transport from tumors to the systemic circulation. We suggest that lymphatic exudate provides a rich source of tumor-derived factors for enabling the discovery of novel biomarkers that may reflect disease stage and therapeutic response. Rockefeller University Press 2019-05-06 2019-04-11 /pmc/articles/PMC6504224/ /pubmed/30975896 http://dx.doi.org/10.1084/jem.20181618 Text en © 2019 Broggi et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Research Articles Broggi, Maria A.S. Maillat, Lea Clement, Cristina C. Bordry, Natacha Corthésy, Patricia Auger, Aymeric Matter, Maurice Hamelin, Romain Potin, Lambert Demurtas, Davide Romano, Emanuela Harari, Alexandre Speiser, Daniel E. Santambrogio, Laura Swartz, Melody A. Tumor-associated factors are enriched in lymphatic exudate compared to plasma in metastatic melanoma patients |
title | Tumor-associated factors are enriched in lymphatic exudate compared to plasma in metastatic melanoma patients |
title_full | Tumor-associated factors are enriched in lymphatic exudate compared to plasma in metastatic melanoma patients |
title_fullStr | Tumor-associated factors are enriched in lymphatic exudate compared to plasma in metastatic melanoma patients |
title_full_unstemmed | Tumor-associated factors are enriched in lymphatic exudate compared to plasma in metastatic melanoma patients |
title_short | Tumor-associated factors are enriched in lymphatic exudate compared to plasma in metastatic melanoma patients |
title_sort | tumor-associated factors are enriched in lymphatic exudate compared to plasma in metastatic melanoma patients |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6504224/ https://www.ncbi.nlm.nih.gov/pubmed/30975896 http://dx.doi.org/10.1084/jem.20181618 |
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