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FAT1: a potential target for monoclonal antibody therapy in colon cancer
BACKGROUND: Colorectal cancer (CRC) is one of the major causes of cancer-associated mortality worldwide. The currently approved therapeutic agents have limited efficacy. METHODS: The atypical cadherin FAT1 was discovered as a novel CRC-associated protein by using a monoclonal antibody (mAb198.3). FA...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931367/ https://www.ncbi.nlm.nih.gov/pubmed/27328312 http://dx.doi.org/10.1038/bjc.2016.145 |
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author | Pileri, Piero Campagnoli, Susanna Grandi, Alberto Parri, Matteo De Camilli, Elisa Song, Chaojun Ganfini, Luisa Lacombe, Aurelien Naldi, Ilaria Sarmientos, Paolo Cinti, Caterina Jin, Boquan Grandi, Guido Viale, Giuseppe Terracciano, Luigi Grifantini, Renata |
author_facet | Pileri, Piero Campagnoli, Susanna Grandi, Alberto Parri, Matteo De Camilli, Elisa Song, Chaojun Ganfini, Luisa Lacombe, Aurelien Naldi, Ilaria Sarmientos, Paolo Cinti, Caterina Jin, Boquan Grandi, Guido Viale, Giuseppe Terracciano, Luigi Grifantini, Renata |
author_sort | Pileri, Piero |
collection | PubMed |
description | BACKGROUND: Colorectal cancer (CRC) is one of the major causes of cancer-associated mortality worldwide. The currently approved therapeutic agents have limited efficacy. METHODS: The atypical cadherin FAT1 was discovered as a novel CRC-associated protein by using a monoclonal antibody (mAb198.3). FAT1 expression was assessed in CRC cells by immunohistochemistry (IHC), immunoblots, flow cytometry and confocal microscopy. In addition, in vitro and in vivo tumour models were done to assess FAT1 potential value for therapeutic applications. RESULTS: The study shows that FAT1 is broadly expressed in primary and metastatic CRC stages and detected by mAb198.3, regardless of KRAS and BRAF mutations. FAT1 mainly accumulates at the plasma membrane of cancer cells, whereas it is only marginally detected in normal human samples. Moreover, the study shows that FAT1 has an important role in cell invasiveness while it does not significantly influence apoptosis. mAb198.3 specifically recognises FAT1 on the surface of colon cancer cells and is efficiently internalised. Furthermore, it reduces cancer growth in a colon cancer xenograft model. CONCLUSIONS: This study provides evidence that FAT1 and mAb198.3 may offer new therapeutic opportunities for CRC including the tumours resistant to current EGFR-targeted therapies. |
format | Online Article Text |
id | pubmed-4931367 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49313672017-06-28 FAT1: a potential target for monoclonal antibody therapy in colon cancer Pileri, Piero Campagnoli, Susanna Grandi, Alberto Parri, Matteo De Camilli, Elisa Song, Chaojun Ganfini, Luisa Lacombe, Aurelien Naldi, Ilaria Sarmientos, Paolo Cinti, Caterina Jin, Boquan Grandi, Guido Viale, Giuseppe Terracciano, Luigi Grifantini, Renata Br J Cancer Translational Therapeutics BACKGROUND: Colorectal cancer (CRC) is one of the major causes of cancer-associated mortality worldwide. The currently approved therapeutic agents have limited efficacy. METHODS: The atypical cadherin FAT1 was discovered as a novel CRC-associated protein by using a monoclonal antibody (mAb198.3). FAT1 expression was assessed in CRC cells by immunohistochemistry (IHC), immunoblots, flow cytometry and confocal microscopy. In addition, in vitro and in vivo tumour models were done to assess FAT1 potential value for therapeutic applications. RESULTS: The study shows that FAT1 is broadly expressed in primary and metastatic CRC stages and detected by mAb198.3, regardless of KRAS and BRAF mutations. FAT1 mainly accumulates at the plasma membrane of cancer cells, whereas it is only marginally detected in normal human samples. Moreover, the study shows that FAT1 has an important role in cell invasiveness while it does not significantly influence apoptosis. mAb198.3 specifically recognises FAT1 on the surface of colon cancer cells and is efficiently internalised. Furthermore, it reduces cancer growth in a colon cancer xenograft model. CONCLUSIONS: This study provides evidence that FAT1 and mAb198.3 may offer new therapeutic opportunities for CRC including the tumours resistant to current EGFR-targeted therapies. Nature Publishing Group 2016-06-28 2016-06-21 /pmc/articles/PMC4931367/ /pubmed/27328312 http://dx.doi.org/10.1038/bjc.2016.145 Text en Copyright © 2016 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Translational Therapeutics Pileri, Piero Campagnoli, Susanna Grandi, Alberto Parri, Matteo De Camilli, Elisa Song, Chaojun Ganfini, Luisa Lacombe, Aurelien Naldi, Ilaria Sarmientos, Paolo Cinti, Caterina Jin, Boquan Grandi, Guido Viale, Giuseppe Terracciano, Luigi Grifantini, Renata FAT1: a potential target for monoclonal antibody therapy in colon cancer |
title | FAT1: a potential target for monoclonal antibody therapy in colon cancer |
title_full | FAT1: a potential target for monoclonal antibody therapy in colon cancer |
title_fullStr | FAT1: a potential target for monoclonal antibody therapy in colon cancer |
title_full_unstemmed | FAT1: a potential target for monoclonal antibody therapy in colon cancer |
title_short | FAT1: a potential target for monoclonal antibody therapy in colon cancer |
title_sort | fat1: a potential target for monoclonal antibody therapy in colon cancer |
topic | Translational Therapeutics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931367/ https://www.ncbi.nlm.nih.gov/pubmed/27328312 http://dx.doi.org/10.1038/bjc.2016.145 |
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