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Label-Free Infrared Spectral Histology of Skin Tissue Part II: Impact of a Lumican-Derived Peptide on Melanoma Growth

Melanoma is the most aggressive type of cutaneous malignancies. In addition to its role as a regulator of extracellular matrix (ECM) integrity, lumican, a small leucine-rich proteoglycan, also exhibits anti-tumor properties in melanoma. This work focuses on the use of infrared spectral imaging (IRSI...

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Autores principales: Brézillon, Stéphane, Untereiner, Valérie, Mohamed, Hossam Taha, Ahallal, Estelle, Proult, Isabelle, Nizet, Pierre, Boulagnon-Rombi, Camille, Sockalingum, Ganesh. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7273845/
https://www.ncbi.nlm.nih.gov/pubmed/32548117
http://dx.doi.org/10.3389/fcell.2020.00377
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author Brézillon, Stéphane
Untereiner, Valérie
Mohamed, Hossam Taha
Ahallal, Estelle
Proult, Isabelle
Nizet, Pierre
Boulagnon-Rombi, Camille
Sockalingum, Ganesh. D.
author_facet Brézillon, Stéphane
Untereiner, Valérie
Mohamed, Hossam Taha
Ahallal, Estelle
Proult, Isabelle
Nizet, Pierre
Boulagnon-Rombi, Camille
Sockalingum, Ganesh. D.
author_sort Brézillon, Stéphane
collection PubMed
description Melanoma is the most aggressive type of cutaneous malignancies. In addition to its role as a regulator of extracellular matrix (ECM) integrity, lumican, a small leucine-rich proteoglycan, also exhibits anti-tumor properties in melanoma. This work focuses on the use of infrared spectral imaging (IRSI) and histopathology (IRSH) to study the effect of lumican-derived peptide (L9Mc) on B16F1 melanoma primary tumor growth. Female C57BL/6 mice were injected with B16F1 cells treated with L9Mc (n = 10) or its scrambled peptide (n = 8), and without peptide (control, n = 9). The melanoma primary tumors were subjected to histological and IR imaging analysis. In addition, immunohistochemical staining was performed using anti-Ki-67 and anti-cleaved caspase-3 antibodies. The IR images were analyzed by common K-means clustering to obtain high-contrast IRSH that allowed identifying different ECM tissue regions from the epidermis to the tumor area, which correlated well with H&E staining. Furthermore, IRSH showed good correlation with immunostaining data obtained with anti-Ki-67 and anti-cleaved caspase-3 antibodies, whereby the L9Mc peptide inhibited cell proliferation and increased strongly apoptosis of B16F1 cells in this mouse model of melanoma primary tumors.
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spelling pubmed-72738452020-06-15 Label-Free Infrared Spectral Histology of Skin Tissue Part II: Impact of a Lumican-Derived Peptide on Melanoma Growth Brézillon, Stéphane Untereiner, Valérie Mohamed, Hossam Taha Ahallal, Estelle Proult, Isabelle Nizet, Pierre Boulagnon-Rombi, Camille Sockalingum, Ganesh. D. Front Cell Dev Biol Cell and Developmental Biology Melanoma is the most aggressive type of cutaneous malignancies. In addition to its role as a regulator of extracellular matrix (ECM) integrity, lumican, a small leucine-rich proteoglycan, also exhibits anti-tumor properties in melanoma. This work focuses on the use of infrared spectral imaging (IRSI) and histopathology (IRSH) to study the effect of lumican-derived peptide (L9Mc) on B16F1 melanoma primary tumor growth. Female C57BL/6 mice were injected with B16F1 cells treated with L9Mc (n = 10) or its scrambled peptide (n = 8), and without peptide (control, n = 9). The melanoma primary tumors were subjected to histological and IR imaging analysis. In addition, immunohistochemical staining was performed using anti-Ki-67 and anti-cleaved caspase-3 antibodies. The IR images were analyzed by common K-means clustering to obtain high-contrast IRSH that allowed identifying different ECM tissue regions from the epidermis to the tumor area, which correlated well with H&E staining. Furthermore, IRSH showed good correlation with immunostaining data obtained with anti-Ki-67 and anti-cleaved caspase-3 antibodies, whereby the L9Mc peptide inhibited cell proliferation and increased strongly apoptosis of B16F1 cells in this mouse model of melanoma primary tumors. Frontiers Media S.A. 2020-05-29 /pmc/articles/PMC7273845/ /pubmed/32548117 http://dx.doi.org/10.3389/fcell.2020.00377 Text en Copyright © 2020 Brézillon, Untereiner, Mohamed, Ahallal, Proult, Nizet, Boulagnon-Rombi and Sockalingum. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Brézillon, Stéphane
Untereiner, Valérie
Mohamed, Hossam Taha
Ahallal, Estelle
Proult, Isabelle
Nizet, Pierre
Boulagnon-Rombi, Camille
Sockalingum, Ganesh. D.
Label-Free Infrared Spectral Histology of Skin Tissue Part II: Impact of a Lumican-Derived Peptide on Melanoma Growth
title Label-Free Infrared Spectral Histology of Skin Tissue Part II: Impact of a Lumican-Derived Peptide on Melanoma Growth
title_full Label-Free Infrared Spectral Histology of Skin Tissue Part II: Impact of a Lumican-Derived Peptide on Melanoma Growth
title_fullStr Label-Free Infrared Spectral Histology of Skin Tissue Part II: Impact of a Lumican-Derived Peptide on Melanoma Growth
title_full_unstemmed Label-Free Infrared Spectral Histology of Skin Tissue Part II: Impact of a Lumican-Derived Peptide on Melanoma Growth
title_short Label-Free Infrared Spectral Histology of Skin Tissue Part II: Impact of a Lumican-Derived Peptide on Melanoma Growth
title_sort label-free infrared spectral histology of skin tissue part ii: impact of a lumican-derived peptide on melanoma growth
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7273845/
https://www.ncbi.nlm.nih.gov/pubmed/32548117
http://dx.doi.org/10.3389/fcell.2020.00377
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