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Mutually exclusive lymphangiogenesis or perineural infiltration in human skin squamous-cell carcinoma

Although tumor-associated lymphangiogenesis correlates with metastasis and poor prognosis in several cancers, it also supports T cell infiltration into the tumor and predicts favorable outcome to immunotherapy. The role of lymphatic vessels in skin squamous-cell carcinoma (sSCC), the second most com...

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Autores principales: Schaller, Julien, Hajjami, Hélène Maby-El, Rusakiewicz, Sylvie, Ioannidou, Kalliopi, Piazzon, Nathalie, Miles, Alexandra, Golshayan, Déla, Gaide, Olivier, Hohl, Daniel, Speiser, Daniel E., Schaeuble, Karin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8021034/
https://www.ncbi.nlm.nih.gov/pubmed/33868585
http://dx.doi.org/10.18632/oncotarget.27915
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author Schaller, Julien
Hajjami, Hélène Maby-El
Rusakiewicz, Sylvie
Ioannidou, Kalliopi
Piazzon, Nathalie
Miles, Alexandra
Golshayan, Déla
Gaide, Olivier
Hohl, Daniel
Speiser, Daniel E.
Schaeuble, Karin
author_facet Schaller, Julien
Hajjami, Hélène Maby-El
Rusakiewicz, Sylvie
Ioannidou, Kalliopi
Piazzon, Nathalie
Miles, Alexandra
Golshayan, Déla
Gaide, Olivier
Hohl, Daniel
Speiser, Daniel E.
Schaeuble, Karin
author_sort Schaller, Julien
collection PubMed
description Although tumor-associated lymphangiogenesis correlates with metastasis and poor prognosis in several cancers, it also supports T cell infiltration into the tumor and predicts favorable outcome to immunotherapy. The role of lymphatic vessels in skin squamous-cell carcinoma (sSCC), the second most common form of skin cancer, remains mostly unknown. Although anti-PD-1 therapy is beneficial for some patients with advanced sSCC, a greater understanding of disease mechanisms is still needed to develop better therapies. Using quantitative multiplex immunohistochemistry, we analyzed sSCC sections from 36 patients. CD8+ T cell infiltration showed great differences between patients, whereby these cells were mainly excluded from the tumor mass. Similar to our data in melanoma, sSCC with high density of lymphatic endothelial cells showed increased CD8+ T cell density in tumor areas. An entirely new observation is that sSCC with perineural infiltration but without metastasis was characterized by low lymphatic endothelial cell density. Since both, metastasis and perineural infiltration are known to affect tumor progression and patients’ prognosis, it is important to identify the molecular drivers, opening future options for therapeutic targeting. Our data suggest that the mechanisms underlying perineural infiltration may be linked with the biology of lymphatic vessels and thus stroma.
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spelling pubmed-80210342021-04-15 Mutually exclusive lymphangiogenesis or perineural infiltration in human skin squamous-cell carcinoma Schaller, Julien Hajjami, Hélène Maby-El Rusakiewicz, Sylvie Ioannidou, Kalliopi Piazzon, Nathalie Miles, Alexandra Golshayan, Déla Gaide, Olivier Hohl, Daniel Speiser, Daniel E. Schaeuble, Karin Oncotarget Research Paper Although tumor-associated lymphangiogenesis correlates with metastasis and poor prognosis in several cancers, it also supports T cell infiltration into the tumor and predicts favorable outcome to immunotherapy. The role of lymphatic vessels in skin squamous-cell carcinoma (sSCC), the second most common form of skin cancer, remains mostly unknown. Although anti-PD-1 therapy is beneficial for some patients with advanced sSCC, a greater understanding of disease mechanisms is still needed to develop better therapies. Using quantitative multiplex immunohistochemistry, we analyzed sSCC sections from 36 patients. CD8+ T cell infiltration showed great differences between patients, whereby these cells were mainly excluded from the tumor mass. Similar to our data in melanoma, sSCC with high density of lymphatic endothelial cells showed increased CD8+ T cell density in tumor areas. An entirely new observation is that sSCC with perineural infiltration but without metastasis was characterized by low lymphatic endothelial cell density. Since both, metastasis and perineural infiltration are known to affect tumor progression and patients’ prognosis, it is important to identify the molecular drivers, opening future options for therapeutic targeting. Our data suggest that the mechanisms underlying perineural infiltration may be linked with the biology of lymphatic vessels and thus stroma. Impact Journals LLC 2021-03-30 /pmc/articles/PMC8021034/ /pubmed/33868585 http://dx.doi.org/10.18632/oncotarget.27915 Text en Copyright: © 2021 Schaller et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Schaller, Julien
Hajjami, Hélène Maby-El
Rusakiewicz, Sylvie
Ioannidou, Kalliopi
Piazzon, Nathalie
Miles, Alexandra
Golshayan, Déla
Gaide, Olivier
Hohl, Daniel
Speiser, Daniel E.
Schaeuble, Karin
Mutually exclusive lymphangiogenesis or perineural infiltration in human skin squamous-cell carcinoma
title Mutually exclusive lymphangiogenesis or perineural infiltration in human skin squamous-cell carcinoma
title_full Mutually exclusive lymphangiogenesis or perineural infiltration in human skin squamous-cell carcinoma
title_fullStr Mutually exclusive lymphangiogenesis or perineural infiltration in human skin squamous-cell carcinoma
title_full_unstemmed Mutually exclusive lymphangiogenesis or perineural infiltration in human skin squamous-cell carcinoma
title_short Mutually exclusive lymphangiogenesis or perineural infiltration in human skin squamous-cell carcinoma
title_sort mutually exclusive lymphangiogenesis or perineural infiltration in human skin squamous-cell carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8021034/
https://www.ncbi.nlm.nih.gov/pubmed/33868585
http://dx.doi.org/10.18632/oncotarget.27915
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