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In vivo evaluation of the early events associated with liver metastasis of circulating cancer cells
The mechanism of metastasis formation remains still largely unknown. Many studies underline the importance and complexity of the initial arrest of the circulating tumour cells in the target organ, a key stage in metastasis occurrence. In our study, we evaluated by visual means the metastasis formati...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2001
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364062/ https://www.ncbi.nlm.nih.gov/pubmed/11487277 http://dx.doi.org/10.1054/bjoc.2001.1911 |
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author | Ding, L Sunamura, M Kodama, T Yamauchi, J Duda, D G Shimamura, H Shibuya, K Takeda, K Matsuno, S |
author_facet | Ding, L Sunamura, M Kodama, T Yamauchi, J Duda, D G Shimamura, H Shibuya, K Takeda, K Matsuno, S |
author_sort | Ding, L |
collection | PubMed |
description | The mechanism of metastasis formation remains still largely unknown. Many studies underline the importance and complexity of the initial arrest of the circulating tumour cells in the target organ, a key stage in metastasis occurrence. In our study, we evaluated by visual means the metastasis formation using an in vivo microscopy system in a murine model. Moreover, we investigated the involvement of P-selectin in these processes using immunohistochemistry and P-selectin knockout mice. The present study offers direct evidence of distinct pathways for tumour metastasis formation by a lymphoma cell – EL-4 and a solid tumour cell – C26. Off-line analysis of the images and histological data confirmed that mechanical entrapment of the solid tumour cell, which had a bigger diameter than that of the liver sinusoids, promoted metastasis without any detectable involvement of adhesion molecules. On the other hand, we observed that lymphoma cells, in spite of their smaller diameter as compared to the sinusoids, promoted liver metastasis as well, but with the essential participation in their arrest of P-selectin, indicating an adhesion molecule-mediated pathway. © 2001 Cancer Research Campaign http://www.bjcancer.com |
format | Text |
id | pubmed-2364062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2001 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23640622009-09-10 In vivo evaluation of the early events associated with liver metastasis of circulating cancer cells Ding, L Sunamura, M Kodama, T Yamauchi, J Duda, D G Shimamura, H Shibuya, K Takeda, K Matsuno, S Br J Cancer Regular Article The mechanism of metastasis formation remains still largely unknown. Many studies underline the importance and complexity of the initial arrest of the circulating tumour cells in the target organ, a key stage in metastasis occurrence. In our study, we evaluated by visual means the metastasis formation using an in vivo microscopy system in a murine model. Moreover, we investigated the involvement of P-selectin in these processes using immunohistochemistry and P-selectin knockout mice. The present study offers direct evidence of distinct pathways for tumour metastasis formation by a lymphoma cell – EL-4 and a solid tumour cell – C26. Off-line analysis of the images and histological data confirmed that mechanical entrapment of the solid tumour cell, which had a bigger diameter than that of the liver sinusoids, promoted metastasis without any detectable involvement of adhesion molecules. On the other hand, we observed that lymphoma cells, in spite of their smaller diameter as compared to the sinusoids, promoted liver metastasis as well, but with the essential participation in their arrest of P-selectin, indicating an adhesion molecule-mediated pathway. © 2001 Cancer Research Campaign http://www.bjcancer.com Nature Publishing Group 2001-08 /pmc/articles/PMC2364062/ /pubmed/11487277 http://dx.doi.org/10.1054/bjoc.2001.1911 Text en Copyright © 2001 Cancer Research Campaign https://creativecommons.org/licenses/by/4.0/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 https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Regular Article Ding, L Sunamura, M Kodama, T Yamauchi, J Duda, D G Shimamura, H Shibuya, K Takeda, K Matsuno, S In vivo evaluation of the early events associated with liver metastasis of circulating cancer cells |
title | In vivo evaluation of the early events associated with liver metastasis of circulating cancer cells |
title_full | In vivo evaluation of the early events associated with liver metastasis of circulating cancer cells |
title_fullStr | In vivo evaluation of the early events associated with liver metastasis of circulating cancer cells |
title_full_unstemmed | In vivo evaluation of the early events associated with liver metastasis of circulating cancer cells |
title_short | In vivo evaluation of the early events associated with liver metastasis of circulating cancer cells |
title_sort | in vivo evaluation of the early events associated with liver metastasis of circulating cancer cells |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364062/ https://www.ncbi.nlm.nih.gov/pubmed/11487277 http://dx.doi.org/10.1054/bjoc.2001.1911 |
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