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The FAK inhibitor BI 853520 exerts anti-tumor effects in breast cancer
Focal adhesion kinase (FAK) is a cytoplasmic tyrosine kinase that regulates a plethora of downstream signaling pathways essential for cell migration, proliferation and death, processes that are exploited by cancer cells during malignant progression. These well-established tumorigenic activities, tog...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148276/ https://www.ncbi.nlm.nih.gov/pubmed/30237500 http://dx.doi.org/10.1038/s41389-018-0083-1 |
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author | Tiede, Stefanie Meyer-Schaller, Nathalie Kalathur, Ravi Kiran Reddy Ivanek, Robert Fagiani, Ernesta Schmassmann, Philip Stillhard, Patrick Häfliger, Simon Kraut, Norbert Schweifer, Norbert Waizenegger, Irene C. Bill, Ruben Christofori, Gerhard |
author_facet | Tiede, Stefanie Meyer-Schaller, Nathalie Kalathur, Ravi Kiran Reddy Ivanek, Robert Fagiani, Ernesta Schmassmann, Philip Stillhard, Patrick Häfliger, Simon Kraut, Norbert Schweifer, Norbert Waizenegger, Irene C. Bill, Ruben Christofori, Gerhard |
author_sort | Tiede, Stefanie |
collection | PubMed |
description | Focal adhesion kinase (FAK) is a cytoplasmic tyrosine kinase that regulates a plethora of downstream signaling pathways essential for cell migration, proliferation and death, processes that are exploited by cancer cells during malignant progression. These well-established tumorigenic activities, together with its high expression and activity in different cancer types, highlight FAK as an attractive target for cancer therapy. We have assessed and characterized the therapeutic potential and the biological effects of BI 853520, a novel small chemical inhibitor of FAK, in several preclinical mouse models of breast cancer. Treatment with BI 853520 elicits a significant reduction in primary tumor growth caused by an anti-proliferative activity by BI 853520. In contrast, BI 853520 exerts effects with varying degrees of robustness on the different stages of the metastatic cascade. Together, the data demonstrate that the repression of FAK activity by the specific FAK inhibitor BI 853520 offers a promising anti-proliferative approach for cancer therapy. |
format | Online Article Text |
id | pubmed-6148276 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61482762018-09-25 The FAK inhibitor BI 853520 exerts anti-tumor effects in breast cancer Tiede, Stefanie Meyer-Schaller, Nathalie Kalathur, Ravi Kiran Reddy Ivanek, Robert Fagiani, Ernesta Schmassmann, Philip Stillhard, Patrick Häfliger, Simon Kraut, Norbert Schweifer, Norbert Waizenegger, Irene C. Bill, Ruben Christofori, Gerhard Oncogenesis Article Focal adhesion kinase (FAK) is a cytoplasmic tyrosine kinase that regulates a plethora of downstream signaling pathways essential for cell migration, proliferation and death, processes that are exploited by cancer cells during malignant progression. These well-established tumorigenic activities, together with its high expression and activity in different cancer types, highlight FAK as an attractive target for cancer therapy. We have assessed and characterized the therapeutic potential and the biological effects of BI 853520, a novel small chemical inhibitor of FAK, in several preclinical mouse models of breast cancer. Treatment with BI 853520 elicits a significant reduction in primary tumor growth caused by an anti-proliferative activity by BI 853520. In contrast, BI 853520 exerts effects with varying degrees of robustness on the different stages of the metastatic cascade. Together, the data demonstrate that the repression of FAK activity by the specific FAK inhibitor BI 853520 offers a promising anti-proliferative approach for cancer therapy. Nature Publishing Group UK 2018-09-20 /pmc/articles/PMC6148276/ /pubmed/30237500 http://dx.doi.org/10.1038/s41389-018-0083-1 Text en © The Author(s) 2018 Open Access 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 http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Tiede, Stefanie Meyer-Schaller, Nathalie Kalathur, Ravi Kiran Reddy Ivanek, Robert Fagiani, Ernesta Schmassmann, Philip Stillhard, Patrick Häfliger, Simon Kraut, Norbert Schweifer, Norbert Waizenegger, Irene C. Bill, Ruben Christofori, Gerhard The FAK inhibitor BI 853520 exerts anti-tumor effects in breast cancer |
title | The FAK inhibitor BI 853520 exerts anti-tumor effects in breast cancer |
title_full | The FAK inhibitor BI 853520 exerts anti-tumor effects in breast cancer |
title_fullStr | The FAK inhibitor BI 853520 exerts anti-tumor effects in breast cancer |
title_full_unstemmed | The FAK inhibitor BI 853520 exerts anti-tumor effects in breast cancer |
title_short | The FAK inhibitor BI 853520 exerts anti-tumor effects in breast cancer |
title_sort | fak inhibitor bi 853520 exerts anti-tumor effects in breast cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148276/ https://www.ncbi.nlm.nih.gov/pubmed/30237500 http://dx.doi.org/10.1038/s41389-018-0083-1 |
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