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Inhibition of breast cancer growth and metastasis by a biomimetic peptide
Metastasis is the main cause of mortality in cancer patients. Though there are many anti-cancer drugs targeting primary tumor growth, anti-metastatic agents are rarely developed. Angiogenesis and lymphangiogenesis are crucial for cancer progression, particularly, lymphangiogenesis is pivotal for met...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4238022/ https://www.ncbi.nlm.nih.gov/pubmed/25409905 http://dx.doi.org/10.1038/srep07139 |
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author | Lee, Esak Lee, Seung Jae Koskimaki, Jacob E. Han, Zheyi Pandey, Niranjan B. Popel, Aleksander S. |
author_facet | Lee, Esak Lee, Seung Jae Koskimaki, Jacob E. Han, Zheyi Pandey, Niranjan B. Popel, Aleksander S. |
author_sort | Lee, Esak |
collection | PubMed |
description | Metastasis is the main cause of mortality in cancer patients. Though there are many anti-cancer drugs targeting primary tumor growth, anti-metastatic agents are rarely developed. Angiogenesis and lymphangiogenesis are crucial for cancer progression, particularly, lymphangiogenesis is pivotal for metastasis in breast cancer. Here we report that a novel collagen IV derived biomimetic peptide inhibits breast cancer growth and metastasis by blocking angiogenesis and lymphangiogenesis. The peptide inhibits blood and lymphatic endothelial cell viability, migration, adhesion, and tube formation by targeting IGF1R and Met signals. The peptide blocks MDA-MB-231 tumor growth by inhibiting tumor angiogenesis in vivo. Moreover, the peptide inhibits lymphangiogenesis in primary tumors. MDA-MB-231 tumor conditioned media (TCM) was employed to accelerate spontaneous metastasis in tumor xenografts, and the anti-metastatic activity of the peptide was tested in this model. The peptide prevents metastasis to the lungs and lymph nodes by inhibiting TCM-induced lymphangiogenesis and angiogenesis in the pre-metastatic organs. In summary, a novel biomimetic peptide inhibits breast cancer growth and metastasis by blocking angiogenesis and lymphangiogenesis in the pre-metastatic organs as well as primary tumors. |
format | Online Article Text |
id | pubmed-4238022 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-42380222014-11-25 Inhibition of breast cancer growth and metastasis by a biomimetic peptide Lee, Esak Lee, Seung Jae Koskimaki, Jacob E. Han, Zheyi Pandey, Niranjan B. Popel, Aleksander S. Sci Rep Article Metastasis is the main cause of mortality in cancer patients. Though there are many anti-cancer drugs targeting primary tumor growth, anti-metastatic agents are rarely developed. Angiogenesis and lymphangiogenesis are crucial for cancer progression, particularly, lymphangiogenesis is pivotal for metastasis in breast cancer. Here we report that a novel collagen IV derived biomimetic peptide inhibits breast cancer growth and metastasis by blocking angiogenesis and lymphangiogenesis. The peptide inhibits blood and lymphatic endothelial cell viability, migration, adhesion, and tube formation by targeting IGF1R and Met signals. The peptide blocks MDA-MB-231 tumor growth by inhibiting tumor angiogenesis in vivo. Moreover, the peptide inhibits lymphangiogenesis in primary tumors. MDA-MB-231 tumor conditioned media (TCM) was employed to accelerate spontaneous metastasis in tumor xenografts, and the anti-metastatic activity of the peptide was tested in this model. The peptide prevents metastasis to the lungs and lymph nodes by inhibiting TCM-induced lymphangiogenesis and angiogenesis in the pre-metastatic organs. In summary, a novel biomimetic peptide inhibits breast cancer growth and metastasis by blocking angiogenesis and lymphangiogenesis in the pre-metastatic organs as well as primary tumors. Nature Publishing Group 2014-11-20 /pmc/articles/PMC4238022/ /pubmed/25409905 http://dx.doi.org/10.1038/srep07139 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 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 in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Article Lee, Esak Lee, Seung Jae Koskimaki, Jacob E. Han, Zheyi Pandey, Niranjan B. Popel, Aleksander S. Inhibition of breast cancer growth and metastasis by a biomimetic peptide |
title | Inhibition of breast cancer growth and metastasis by a biomimetic peptide |
title_full | Inhibition of breast cancer growth and metastasis by a biomimetic peptide |
title_fullStr | Inhibition of breast cancer growth and metastasis by a biomimetic peptide |
title_full_unstemmed | Inhibition of breast cancer growth and metastasis by a biomimetic peptide |
title_short | Inhibition of breast cancer growth and metastasis by a biomimetic peptide |
title_sort | inhibition of breast cancer growth and metastasis by a biomimetic peptide |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4238022/ https://www.ncbi.nlm.nih.gov/pubmed/25409905 http://dx.doi.org/10.1038/srep07139 |
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