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Tumor endothelial marker 8 promotes cancer progression and metastasis
Every year more than 8 million people suffer from cancer-related deaths worldwide [1]. Metastasis, the spread of cancer to distant sites, accounts for 90% of these deaths. A promising target for blocking tumor progression, without causing severe side effects [2], is Tumor Endothelial Marker 8 (TEM8)...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6059023/ https://www.ncbi.nlm.nih.gov/pubmed/30046396 http://dx.doi.org/10.18632/oncotarget.25734 |
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author | Høye, Anette M. Tolstrup, Sofie D. Horton, Edward R. Nicolau, Monica Frost, Helen Woo, Jung H. Mauldin, Jeremy P. Frankel, Arthur E. Cox, Thomas R. Erler, Janine T. |
author_facet | Høye, Anette M. Tolstrup, Sofie D. Horton, Edward R. Nicolau, Monica Frost, Helen Woo, Jung H. Mauldin, Jeremy P. Frankel, Arthur E. Cox, Thomas R. Erler, Janine T. |
author_sort | Høye, Anette M. |
collection | PubMed |
description | Every year more than 8 million people suffer from cancer-related deaths worldwide [1]. Metastasis, the spread of cancer to distant sites, accounts for 90% of these deaths. A promising target for blocking tumor progression, without causing severe side effects [2], is Tumor Endothelial Marker 8 (TEM8), an integrin-like cell surface protein expressed predominantly in the tumor endothelium and in cancer cells [3, 4]. Here, we have investigated the role of TEM8 in cancer progression, angiogenesis and metastasis in invasive breast cancer, and validated the main findings and important results in colorectal cancer. We show that the loss of TEM8 in cancer cells results in inhibition of cancer progression, reduction in tumor angiogenesis and reduced metastatic burden in breast cancer mouse models. Furthermore, we show that TEM8 regulates cancer progression by affecting the expression levels of cell cycle-related genes. Taken together, our findings may have broad clinical and therapeutic potential for breast and colorectal primary tumor and metastasis treatment by targeting TEM8. |
format | Online Article Text |
id | pubmed-6059023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-60590232018-07-25 Tumor endothelial marker 8 promotes cancer progression and metastasis Høye, Anette M. Tolstrup, Sofie D. Horton, Edward R. Nicolau, Monica Frost, Helen Woo, Jung H. Mauldin, Jeremy P. Frankel, Arthur E. Cox, Thomas R. Erler, Janine T. Oncotarget Research Paper Every year more than 8 million people suffer from cancer-related deaths worldwide [1]. Metastasis, the spread of cancer to distant sites, accounts for 90% of these deaths. A promising target for blocking tumor progression, without causing severe side effects [2], is Tumor Endothelial Marker 8 (TEM8), an integrin-like cell surface protein expressed predominantly in the tumor endothelium and in cancer cells [3, 4]. Here, we have investigated the role of TEM8 in cancer progression, angiogenesis and metastasis in invasive breast cancer, and validated the main findings and important results in colorectal cancer. We show that the loss of TEM8 in cancer cells results in inhibition of cancer progression, reduction in tumor angiogenesis and reduced metastatic burden in breast cancer mouse models. Furthermore, we show that TEM8 regulates cancer progression by affecting the expression levels of cell cycle-related genes. Taken together, our findings may have broad clinical and therapeutic potential for breast and colorectal primary tumor and metastasis treatment by targeting TEM8. Impact Journals LLC 2018-07-10 /pmc/articles/PMC6059023/ /pubmed/30046396 http://dx.doi.org/10.18632/oncotarget.25734 Text en Copyright: © 2018 Høye et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Høye, Anette M. Tolstrup, Sofie D. Horton, Edward R. Nicolau, Monica Frost, Helen Woo, Jung H. Mauldin, Jeremy P. Frankel, Arthur E. Cox, Thomas R. Erler, Janine T. Tumor endothelial marker 8 promotes cancer progression and metastasis |
title | Tumor endothelial marker 8 promotes cancer progression and metastasis |
title_full | Tumor endothelial marker 8 promotes cancer progression and metastasis |
title_fullStr | Tumor endothelial marker 8 promotes cancer progression and metastasis |
title_full_unstemmed | Tumor endothelial marker 8 promotes cancer progression and metastasis |
title_short | Tumor endothelial marker 8 promotes cancer progression and metastasis |
title_sort | tumor endothelial marker 8 promotes cancer progression and metastasis |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6059023/ https://www.ncbi.nlm.nih.gov/pubmed/30046396 http://dx.doi.org/10.18632/oncotarget.25734 |
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