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Small Molecules Antagonise the MIA-Fibronectin Interaction in Malignant Melanoma
Melanoma inhibitory activity (MIA), an extracellular protein highly expressed by malignant melanoma cells, plays an important functional role in melanoma development, progression, and metastasis. After its secretion, MIA directly interacts with extracellular matrix proteins, such as fibronectin (FN)...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4858652/ https://www.ncbi.nlm.nih.gov/pubmed/27151361 http://dx.doi.org/10.1038/srep25119 |
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author | Yip, King Tuo Zhong, Xue Yin Seibel, Nadia Pütz, Stefanie Autzen, Jasmin Gasper, Raphael Hofmann, Eckhard Scherkenbeck, Jürgen Stoll, Raphael |
author_facet | Yip, King Tuo Zhong, Xue Yin Seibel, Nadia Pütz, Stefanie Autzen, Jasmin Gasper, Raphael Hofmann, Eckhard Scherkenbeck, Jürgen Stoll, Raphael |
author_sort | Yip, King Tuo |
collection | PubMed |
description | Melanoma inhibitory activity (MIA), an extracellular protein highly expressed by malignant melanoma cells, plays an important functional role in melanoma development, progression, and metastasis. After its secretion, MIA directly interacts with extracellular matrix proteins, such as fibronectin (FN). By this mechanism, MIA actively facilitates focal cell detachment from surrounding structures and strongly promotes tumour cell invasion and migration. Hence, the molecular understanding of MIA’s function provides a promising target for the development of new strategies in malignant melanoma therapy. Here, we describe for the first time the discovery of small molecules that are able to disrupt the MIA-FN complex by selectively binding to a new druggable pocket, which we could identify on MIA by structural analysis and fragment-based screening. Our findings may inspire novel drug discovery efforts aiming at a therapeutically effective treatment of melanoma by targeting MIA. |
format | Online Article Text |
id | pubmed-4858652 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48586522016-05-19 Small Molecules Antagonise the MIA-Fibronectin Interaction in Malignant Melanoma Yip, King Tuo Zhong, Xue Yin Seibel, Nadia Pütz, Stefanie Autzen, Jasmin Gasper, Raphael Hofmann, Eckhard Scherkenbeck, Jürgen Stoll, Raphael Sci Rep Article Melanoma inhibitory activity (MIA), an extracellular protein highly expressed by malignant melanoma cells, plays an important functional role in melanoma development, progression, and metastasis. After its secretion, MIA directly interacts with extracellular matrix proteins, such as fibronectin (FN). By this mechanism, MIA actively facilitates focal cell detachment from surrounding structures and strongly promotes tumour cell invasion and migration. Hence, the molecular understanding of MIA’s function provides a promising target for the development of new strategies in malignant melanoma therapy. Here, we describe for the first time the discovery of small molecules that are able to disrupt the MIA-FN complex by selectively binding to a new druggable pocket, which we could identify on MIA by structural analysis and fragment-based screening. Our findings may inspire novel drug discovery efforts aiming at a therapeutically effective treatment of melanoma by targeting MIA. Nature Publishing Group 2016-05-06 /pmc/articles/PMC4858652/ /pubmed/27151361 http://dx.doi.org/10.1038/srep25119 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Yip, King Tuo Zhong, Xue Yin Seibel, Nadia Pütz, Stefanie Autzen, Jasmin Gasper, Raphael Hofmann, Eckhard Scherkenbeck, Jürgen Stoll, Raphael Small Molecules Antagonise the MIA-Fibronectin Interaction in Malignant Melanoma |
title | Small Molecules Antagonise the MIA-Fibronectin Interaction in Malignant Melanoma |
title_full | Small Molecules Antagonise the MIA-Fibronectin Interaction in Malignant Melanoma |
title_fullStr | Small Molecules Antagonise the MIA-Fibronectin Interaction in Malignant Melanoma |
title_full_unstemmed | Small Molecules Antagonise the MIA-Fibronectin Interaction in Malignant Melanoma |
title_short | Small Molecules Antagonise the MIA-Fibronectin Interaction in Malignant Melanoma |
title_sort | small molecules antagonise the mia-fibronectin interaction in malignant melanoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4858652/ https://www.ncbi.nlm.nih.gov/pubmed/27151361 http://dx.doi.org/10.1038/srep25119 |
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