Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
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
_version_ 1782440878103592960
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
work_keys_str_mv AT pileripiero fat1apotentialtargetformonoclonalantibodytherapyincoloncancer
AT campagnolisusanna fat1apotentialtargetformonoclonalantibodytherapyincoloncancer
AT grandialberto fat1apotentialtargetformonoclonalantibodytherapyincoloncancer
AT parrimatteo fat1apotentialtargetformonoclonalantibodytherapyincoloncancer
AT decamillielisa fat1apotentialtargetformonoclonalantibodytherapyincoloncancer
AT songchaojun fat1apotentialtargetformonoclonalantibodytherapyincoloncancer
AT ganfiniluisa fat1apotentialtargetformonoclonalantibodytherapyincoloncancer
AT lacombeaurelien fat1apotentialtargetformonoclonalantibodytherapyincoloncancer
AT naldiilaria fat1apotentialtargetformonoclonalantibodytherapyincoloncancer
AT sarmientospaolo fat1apotentialtargetformonoclonalantibodytherapyincoloncancer
AT cinticaterina fat1apotentialtargetformonoclonalantibodytherapyincoloncancer
AT jinboquan fat1apotentialtargetformonoclonalantibodytherapyincoloncancer
AT grandiguido fat1apotentialtargetformonoclonalantibodytherapyincoloncancer
AT vialegiuseppe fat1apotentialtargetformonoclonalantibodytherapyincoloncancer
AT terraccianoluigi fat1apotentialtargetformonoclonalantibodytherapyincoloncancer
AT grifantinirenata fat1apotentialtargetformonoclonalantibodytherapyincoloncancer