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A complex of α(6) integrin and E-cadherin drives liver metastasis of colorectal cancer cells through hepatic angiopoietin-like 6
Homing of colorectal cancer (CRC) cells to the liver is a non-random process driven by a crosstalk between tumour cells and components of the host tissue. Here we report the isolation of a liver metastasis-specific peptide ligand (CGIYRLRSC) that binds a complex of E-cadherin and α(6) integrin on th...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY-VCH Verlag
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3494873/ https://www.ncbi.nlm.nih.gov/pubmed/23070965 http://dx.doi.org/10.1002/emmm.201101164 |
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author | Marchiò, Serena Soster, Marco Cardaci, Sabrina Muratore, Andrea Bartolini, Alice Barone, Vanessa Ribero, Dario Monti, Maria Bovino, Paola Sun, Jessica Giavazzi, Raffaella Asioli, Sofia Cassoni, Paola Capussotti, Lorenzo Pucci, Piero Bugatti, Antonella Rusnati, Marco Pasqualini, Renata Arap, Wadih Bussolino, Federico |
author_facet | Marchiò, Serena Soster, Marco Cardaci, Sabrina Muratore, Andrea Bartolini, Alice Barone, Vanessa Ribero, Dario Monti, Maria Bovino, Paola Sun, Jessica Giavazzi, Raffaella Asioli, Sofia Cassoni, Paola Capussotti, Lorenzo Pucci, Piero Bugatti, Antonella Rusnati, Marco Pasqualini, Renata Arap, Wadih Bussolino, Federico |
author_sort | Marchiò, Serena |
collection | PubMed |
description | Homing of colorectal cancer (CRC) cells to the liver is a non-random process driven by a crosstalk between tumour cells and components of the host tissue. Here we report the isolation of a liver metastasis-specific peptide ligand (CGIYRLRSC) that binds a complex of E-cadherin and α(6) integrin on the surface of CRC cells. We identify angiopoietin-like 6 protein as a peptide-mimicked natural ligand enriched in hepatic blood vessels of CRC patients. We demonstrate that an interaction between hepatic angiopoietin-like 6 and tumoural α(6) integrin/E-cadherin drives liver homing and colonization by CRC cells, and that CGIYRLRSC inhibits liver metastasis through interference with this ligand/receptor system. Our results indicate a mechanism for metastasis whereby a soluble factor accumulated in normal vessels functions as a specific ligand for circulating cancer cells. Consistently, we show that high amounts of coexpressed α(6) integrin and E-cadherin in primary tumours represent a poor prognostic factor for patients with advanced CRC. |
format | Online Article Text |
id | pubmed-3494873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | WILEY-VCH Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-34948732012-11-13 A complex of α(6) integrin and E-cadherin drives liver metastasis of colorectal cancer cells through hepatic angiopoietin-like 6 Marchiò, Serena Soster, Marco Cardaci, Sabrina Muratore, Andrea Bartolini, Alice Barone, Vanessa Ribero, Dario Monti, Maria Bovino, Paola Sun, Jessica Giavazzi, Raffaella Asioli, Sofia Cassoni, Paola Capussotti, Lorenzo Pucci, Piero Bugatti, Antonella Rusnati, Marco Pasqualini, Renata Arap, Wadih Bussolino, Federico EMBO Mol Med Research Articles Homing of colorectal cancer (CRC) cells to the liver is a non-random process driven by a crosstalk between tumour cells and components of the host tissue. Here we report the isolation of a liver metastasis-specific peptide ligand (CGIYRLRSC) that binds a complex of E-cadherin and α(6) integrin on the surface of CRC cells. We identify angiopoietin-like 6 protein as a peptide-mimicked natural ligand enriched in hepatic blood vessels of CRC patients. We demonstrate that an interaction between hepatic angiopoietin-like 6 and tumoural α(6) integrin/E-cadherin drives liver homing and colonization by CRC cells, and that CGIYRLRSC inhibits liver metastasis through interference with this ligand/receptor system. Our results indicate a mechanism for metastasis whereby a soluble factor accumulated in normal vessels functions as a specific ligand for circulating cancer cells. Consistently, we show that high amounts of coexpressed α(6) integrin and E-cadherin in primary tumours represent a poor prognostic factor for patients with advanced CRC. WILEY-VCH Verlag 2012-11 2012-10-16 /pmc/articles/PMC3494873/ /pubmed/23070965 http://dx.doi.org/10.1002/emmm.201101164 Text en Copyright © 2012 The Authors. Published by John Wiley and Sons, Ltd on behalf of EMBO http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Research Articles Marchiò, Serena Soster, Marco Cardaci, Sabrina Muratore, Andrea Bartolini, Alice Barone, Vanessa Ribero, Dario Monti, Maria Bovino, Paola Sun, Jessica Giavazzi, Raffaella Asioli, Sofia Cassoni, Paola Capussotti, Lorenzo Pucci, Piero Bugatti, Antonella Rusnati, Marco Pasqualini, Renata Arap, Wadih Bussolino, Federico A complex of α(6) integrin and E-cadherin drives liver metastasis of colorectal cancer cells through hepatic angiopoietin-like 6 |
title | A complex of α(6) integrin and E-cadherin drives liver metastasis of colorectal cancer cells through hepatic angiopoietin-like 6 |
title_full | A complex of α(6) integrin and E-cadherin drives liver metastasis of colorectal cancer cells through hepatic angiopoietin-like 6 |
title_fullStr | A complex of α(6) integrin and E-cadherin drives liver metastasis of colorectal cancer cells through hepatic angiopoietin-like 6 |
title_full_unstemmed | A complex of α(6) integrin and E-cadherin drives liver metastasis of colorectal cancer cells through hepatic angiopoietin-like 6 |
title_short | A complex of α(6) integrin and E-cadherin drives liver metastasis of colorectal cancer cells through hepatic angiopoietin-like 6 |
title_sort | complex of α(6) integrin and e-cadherin drives liver metastasis of colorectal cancer cells through hepatic angiopoietin-like 6 |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3494873/ https://www.ncbi.nlm.nih.gov/pubmed/23070965 http://dx.doi.org/10.1002/emmm.201101164 |
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