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Expression and functional role of CRIPTO-1 in cutaneous melanoma

BACKGROUND: CRIPTO-1 (CR-1) is involved in the pathogenesis and progression of human carcinoma of different histological origin. In this study we addressed the expression and the functional role of CR-1 in cutaneous melanoma. METHODS: Expression of CR-1 protein in melanomas and melanoma cell lines w...

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Autores principales: De Luca, A, Lamura, L, Strizzi, L, Roma, C, D'Antonio, A, Margaryan, N, Pirozzi, G, Hsu, M-Y, Botti, G, Mari, E, Hendrix, M J C, Salomon, D S, Normanno, N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185940/
https://www.ncbi.nlm.nih.gov/pubmed/21863025
http://dx.doi.org/10.1038/bjc.2011.324
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author De Luca, A
Lamura, L
Strizzi, L
Roma, C
D'Antonio, A
Margaryan, N
Pirozzi, G
Hsu, M-Y
Botti, G
Mari, E
Hendrix, M J C
Salomon, D S
Normanno, N
author_facet De Luca, A
Lamura, L
Strizzi, L
Roma, C
D'Antonio, A
Margaryan, N
Pirozzi, G
Hsu, M-Y
Botti, G
Mari, E
Hendrix, M J C
Salomon, D S
Normanno, N
author_sort De Luca, A
collection PubMed
description BACKGROUND: CRIPTO-1 (CR-1) is involved in the pathogenesis and progression of human carcinoma of different histological origin. In this study we addressed the expression and the functional role of CR-1 in cutaneous melanoma. METHODS: Expression of CR-1 protein in melanomas and melanoma cell lines was assessed by immunohistochemistry, western blotting and/or flow cytometry. Levels of mRNA were evaluated by real-time PCR. Invasion assays were performed in Matrigel-coated modified Boyden chambers. RESULTS: Expression of CR-1 protein and/or mRNA was found in 16 out of 37 primary human cutaneous melanomas and in 12 out of 21 melanoma cell lines. Recombinant CR-1 protein activated in melanoma cells c-Src and, at lesser extent, Smad signalling. In addition, CR-1 significantly increased the invasive ability of melanoma cells that was prevented by treatment with either the ALK4 inhibitor SB-431542 or the c-Src inhibitor saracatinib (AZD0530). Anti-CR-1 siRNAs produced a significant inhibition of the growth and the invasive ability of melanoma cells. Finally, a close correlation was found in melanoma cells between the levels of expression of CR-1 and the effects of saracatinib on cell growth. CONCLUSION: These data indicate that a significant fraction of cutaneous melanoma expresses CR-1 and that this growth factor is involved in the invasion and proliferation of melanoma cells.
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spelling pubmed-31859402012-09-27 Expression and functional role of CRIPTO-1 in cutaneous melanoma De Luca, A Lamura, L Strizzi, L Roma, C D'Antonio, A Margaryan, N Pirozzi, G Hsu, M-Y Botti, G Mari, E Hendrix, M J C Salomon, D S Normanno, N Br J Cancer Molecular Diagnostics BACKGROUND: CRIPTO-1 (CR-1) is involved in the pathogenesis and progression of human carcinoma of different histological origin. In this study we addressed the expression and the functional role of CR-1 in cutaneous melanoma. METHODS: Expression of CR-1 protein in melanomas and melanoma cell lines was assessed by immunohistochemistry, western blotting and/or flow cytometry. Levels of mRNA were evaluated by real-time PCR. Invasion assays were performed in Matrigel-coated modified Boyden chambers. RESULTS: Expression of CR-1 protein and/or mRNA was found in 16 out of 37 primary human cutaneous melanomas and in 12 out of 21 melanoma cell lines. Recombinant CR-1 protein activated in melanoma cells c-Src and, at lesser extent, Smad signalling. In addition, CR-1 significantly increased the invasive ability of melanoma cells that was prevented by treatment with either the ALK4 inhibitor SB-431542 or the c-Src inhibitor saracatinib (AZD0530). Anti-CR-1 siRNAs produced a significant inhibition of the growth and the invasive ability of melanoma cells. Finally, a close correlation was found in melanoma cells between the levels of expression of CR-1 and the effects of saracatinib on cell growth. CONCLUSION: These data indicate that a significant fraction of cutaneous melanoma expresses CR-1 and that this growth factor is involved in the invasion and proliferation of melanoma cells. Nature Publishing Group 2011-09-27 2011-08-23 /pmc/articles/PMC3185940/ /pubmed/21863025 http://dx.doi.org/10.1038/bjc.2011.324 Text en Copyright © 2011 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This 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 license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license 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 license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Molecular Diagnostics
De Luca, A
Lamura, L
Strizzi, L
Roma, C
D'Antonio, A
Margaryan, N
Pirozzi, G
Hsu, M-Y
Botti, G
Mari, E
Hendrix, M J C
Salomon, D S
Normanno, N
Expression and functional role of CRIPTO-1 in cutaneous melanoma
title Expression and functional role of CRIPTO-1 in cutaneous melanoma
title_full Expression and functional role of CRIPTO-1 in cutaneous melanoma
title_fullStr Expression and functional role of CRIPTO-1 in cutaneous melanoma
title_full_unstemmed Expression and functional role of CRIPTO-1 in cutaneous melanoma
title_short Expression and functional role of CRIPTO-1 in cutaneous melanoma
title_sort expression and functional role of cripto-1 in cutaneous melanoma
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185940/
https://www.ncbi.nlm.nih.gov/pubmed/21863025
http://dx.doi.org/10.1038/bjc.2011.324
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