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Cancer cell-derived von Willebrand factor enhanced metastasis of gastric adenocarcinoma
Cancer prognosis is poor for patients with blood-borne metastasis. Platelets are known to assist cancer cells in transmigrating through the endothelium, but ligands for the platelet-mediated cancer metastasis remain poorly defined. von Willebrand factor (vWF) is a major platelet ligand that has been...
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/PMC5833464/ https://www.ncbi.nlm.nih.gov/pubmed/29362409 http://dx.doi.org/10.1038/s41389-017-0023-5 |
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author | Yang, Ai-jun Wang, Min Wang, Yan Cai, Wei Li, Qiang Zhao, Ting-ting Zhang, Li-han Houck, Katie Chen, Xu Jin, Yan-ling Mu, Ji-ying Dong, Jing-fei Li, Min |
author_facet | Yang, Ai-jun Wang, Min Wang, Yan Cai, Wei Li, Qiang Zhao, Ting-ting Zhang, Li-han Houck, Katie Chen, Xu Jin, Yan-ling Mu, Ji-ying Dong, Jing-fei Li, Min |
author_sort | Yang, Ai-jun |
collection | PubMed |
description | Cancer prognosis is poor for patients with blood-borne metastasis. Platelets are known to assist cancer cells in transmigrating through the endothelium, but ligands for the platelet-mediated cancer metastasis remain poorly defined. von Willebrand factor (vWF) is a major platelet ligand that has been widely used as a biomarker in cancer and associated inflammation. However, its functional role in cancer growth and metastasis is largely unknown. Here we report that gastric cancer cells from patients and cells from two well-established gastric cancer lines express vWF and secrete it into the circulation, upon which it rapidly becomes cell-bound to mediate cancer-cell aggregation and interaction with platelets and endothelial cells. The vWF-mediated homotypic and heterotypic cell–cell interactions promote the pulmonary graft of vWF-overexpressing gastric cancer BGC823 cells in a mouse model. The metastasis-promoting activity of vWF was blocked by antibodies against vWF and its platelet receptor GP Ibα. It was also reduced by an inhibitory siRNA that suppresses vWF expression. These findings demonstrate a causal role of cancer-cell-derived vWF in mediating gastric cancer metastasis and identify vWF as a new therapeutic target. |
format | Online Article Text |
id | pubmed-5833464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58334642018-03-06 Cancer cell-derived von Willebrand factor enhanced metastasis of gastric adenocarcinoma Yang, Ai-jun Wang, Min Wang, Yan Cai, Wei Li, Qiang Zhao, Ting-ting Zhang, Li-han Houck, Katie Chen, Xu Jin, Yan-ling Mu, Ji-ying Dong, Jing-fei Li, Min Oncogenesis Article Cancer prognosis is poor for patients with blood-borne metastasis. Platelets are known to assist cancer cells in transmigrating through the endothelium, but ligands for the platelet-mediated cancer metastasis remain poorly defined. von Willebrand factor (vWF) is a major platelet ligand that has been widely used as a biomarker in cancer and associated inflammation. However, its functional role in cancer growth and metastasis is largely unknown. Here we report that gastric cancer cells from patients and cells from two well-established gastric cancer lines express vWF and secrete it into the circulation, upon which it rapidly becomes cell-bound to mediate cancer-cell aggregation and interaction with platelets and endothelial cells. The vWF-mediated homotypic and heterotypic cell–cell interactions promote the pulmonary graft of vWF-overexpressing gastric cancer BGC823 cells in a mouse model. The metastasis-promoting activity of vWF was blocked by antibodies against vWF and its platelet receptor GP Ibα. It was also reduced by an inhibitory siRNA that suppresses vWF expression. These findings demonstrate a causal role of cancer-cell-derived vWF in mediating gastric cancer metastasis and identify vWF as a new therapeutic target. Nature Publishing Group UK 2018-01-24 /pmc/articles/PMC5833464/ /pubmed/29362409 http://dx.doi.org/10.1038/s41389-017-0023-5 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 Yang, Ai-jun Wang, Min Wang, Yan Cai, Wei Li, Qiang Zhao, Ting-ting Zhang, Li-han Houck, Katie Chen, Xu Jin, Yan-ling Mu, Ji-ying Dong, Jing-fei Li, Min Cancer cell-derived von Willebrand factor enhanced metastasis of gastric adenocarcinoma |
title | Cancer cell-derived von Willebrand factor enhanced metastasis of gastric adenocarcinoma |
title_full | Cancer cell-derived von Willebrand factor enhanced metastasis of gastric adenocarcinoma |
title_fullStr | Cancer cell-derived von Willebrand factor enhanced metastasis of gastric adenocarcinoma |
title_full_unstemmed | Cancer cell-derived von Willebrand factor enhanced metastasis of gastric adenocarcinoma |
title_short | Cancer cell-derived von Willebrand factor enhanced metastasis of gastric adenocarcinoma |
title_sort | cancer cell-derived von willebrand factor enhanced metastasis of gastric adenocarcinoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833464/ https://www.ncbi.nlm.nih.gov/pubmed/29362409 http://dx.doi.org/10.1038/s41389-017-0023-5 |
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