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CTGF is overexpressed in malignant melanoma and promotes cell invasion and migration

BACKGROUND: Malignant melanoma cells are known to have altered expression of growth factors compared with normal human melanocytes. These changes most likely favour tumour growth and progression, and influence tumour environment. The induction of transforming growth factor beta1, 2 and 3 as well as...

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Autores principales: Braig, S, Wallner, S, Junglas, B, Fuchshofer, R, Bosserhoff, A-K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3142806/
https://www.ncbi.nlm.nih.gov/pubmed/21673687
http://dx.doi.org/10.1038/bjc.2011.226
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author Braig, S
Wallner, S
Junglas, B
Fuchshofer, R
Bosserhoff, A-K
author_facet Braig, S
Wallner, S
Junglas, B
Fuchshofer, R
Bosserhoff, A-K
author_sort Braig, S
collection PubMed
description BACKGROUND: Malignant melanoma cells are known to have altered expression of growth factors compared with normal human melanocytes. These changes most likely favour tumour growth and progression, and influence tumour environment. The induction of transforming growth factor beta1, 2 and 3 as well as BMP4 and BMP7 expression in malignant melanoma has been reported before, whereas the expression of an important modulator of these molecules, connective tissue growth factor (CTGF), has not been investigated in melanomas until now. METHODS: Expression of CTGF was analysed in melanoma cell lines and tissue samples by qRT–PCR and immunohistochemistry. To determine the regulation of CTGF expression in malignant melanoma, specific siRNA was used. Additionally, migration, invasion and attachment assays were carried out. RESULTS: We were able to demonstrate that CTGF expression is upregulated in nine melanoma cell lines and in primary and metastatic melanoma in situ. The transcription factor HIF-1α was revealed as a positive regulator for CTGF expression. Melanoma cells, in which CTGF expression is diminished, show a strong reduction of migratory and invasive properties when compared with controls. Further, treatment of normal human epidermal melanocytes with recombinant CTGF leads to an increase of migratory and invasive behaviour of these cells. CONCLUSION: These results suggest that CTGF promotes melanoma cell invasion and migration and, therefore, has an important role in the progression of malignant melanoma.
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spelling pubmed-31428062012-07-12 CTGF is overexpressed in malignant melanoma and promotes cell invasion and migration Braig, S Wallner, S Junglas, B Fuchshofer, R Bosserhoff, A-K Br J Cancer Molecular Diagnostics BACKGROUND: Malignant melanoma cells are known to have altered expression of growth factors compared with normal human melanocytes. These changes most likely favour tumour growth and progression, and influence tumour environment. The induction of transforming growth factor beta1, 2 and 3 as well as BMP4 and BMP7 expression in malignant melanoma has been reported before, whereas the expression of an important modulator of these molecules, connective tissue growth factor (CTGF), has not been investigated in melanomas until now. METHODS: Expression of CTGF was analysed in melanoma cell lines and tissue samples by qRT–PCR and immunohistochemistry. To determine the regulation of CTGF expression in malignant melanoma, specific siRNA was used. Additionally, migration, invasion and attachment assays were carried out. RESULTS: We were able to demonstrate that CTGF expression is upregulated in nine melanoma cell lines and in primary and metastatic melanoma in situ. The transcription factor HIF-1α was revealed as a positive regulator for CTGF expression. Melanoma cells, in which CTGF expression is diminished, show a strong reduction of migratory and invasive properties when compared with controls. Further, treatment of normal human epidermal melanocytes with recombinant CTGF leads to an increase of migratory and invasive behaviour of these cells. CONCLUSION: These results suggest that CTGF promotes melanoma cell invasion and migration and, therefore, has an important role in the progression of malignant melanoma. Nature Publishing Group 2011-07-12 2011-06-14 /pmc/articles/PMC3142806/ /pubmed/21673687 http://dx.doi.org/10.1038/bjc.2011.226 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
Braig, S
Wallner, S
Junglas, B
Fuchshofer, R
Bosserhoff, A-K
CTGF is overexpressed in malignant melanoma and promotes cell invasion and migration
title CTGF is overexpressed in malignant melanoma and promotes cell invasion and migration
title_full CTGF is overexpressed in malignant melanoma and promotes cell invasion and migration
title_fullStr CTGF is overexpressed in malignant melanoma and promotes cell invasion and migration
title_full_unstemmed CTGF is overexpressed in malignant melanoma and promotes cell invasion and migration
title_short CTGF is overexpressed in malignant melanoma and promotes cell invasion and migration
title_sort ctgf is overexpressed in malignant melanoma and promotes cell invasion and migration
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3142806/
https://www.ncbi.nlm.nih.gov/pubmed/21673687
http://dx.doi.org/10.1038/bjc.2011.226
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