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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)...

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Autores principales: Yip, King Tuo, Zhong, Xue Yin, Seibel, Nadia, Pütz, Stefanie, Autzen, Jasmin, Gasper, Raphael, Hofmann, Eckhard, Scherkenbeck, Jürgen, Stoll, Raphael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
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.
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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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