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LIN7A is a major determinant of cell-polarity defects in breast carcinomas

BACKGROUND: Polarity defects are a hallmark of most carcinomas. Cells from invasive micropapillary carcinomas (IMPCs) of the breast are characterized by a striking cell polarity inversion and represent an interesting model for the analysis of polarity abnormalities. METHODS: In-depth investigation o...

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Autores principales: Gruel, Nadège, Fuhrmann, Laetitia, Lodillinsky, Catalina, Benhamo, Vanessa, Mariani, Odette, Cédenot, Aurélie, Arnould, Laurent, Macgrogan, Gaëtan, Sastre-Garau, Xavier, Chavrier, Philippe, Delattre, Olivier, Vincent-Salomon, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756502/
https://www.ncbi.nlm.nih.gov/pubmed/26887652
http://dx.doi.org/10.1186/s13058-016-0680-x
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author Gruel, Nadège
Fuhrmann, Laetitia
Lodillinsky, Catalina
Benhamo, Vanessa
Mariani, Odette
Cédenot, Aurélie
Arnould, Laurent
Macgrogan, Gaëtan
Sastre-Garau, Xavier
Chavrier, Philippe
Delattre, Olivier
Vincent-Salomon, Anne
author_facet Gruel, Nadège
Fuhrmann, Laetitia
Lodillinsky, Catalina
Benhamo, Vanessa
Mariani, Odette
Cédenot, Aurélie
Arnould, Laurent
Macgrogan, Gaëtan
Sastre-Garau, Xavier
Chavrier, Philippe
Delattre, Olivier
Vincent-Salomon, Anne
author_sort Gruel, Nadège
collection PubMed
description BACKGROUND: Polarity defects are a hallmark of most carcinomas. Cells from invasive micropapillary carcinomas (IMPCs) of the breast are characterized by a striking cell polarity inversion and represent an interesting model for the analysis of polarity abnormalities. METHODS: In-depth investigation of polarity proteins in 24 IMPCs and a gene expression profiling, comparing IMPC (n = 73) with invasive carcinomas of no special type (ICNST) (n = 51) have been performed. RESULTS: IMPCs showed a profound disorganization of the investigated polarity proteins and revealed major abnormalities in their subcellular localization. Gene expression profiling experiments highlighted a number of deregulated genes in the IMPCs that have a role in apico-basal polarity, adhesion and migration. LIN7A, a Crumbs-complex polarity gene, was one of the most differentially over-expressed genes in the IMPCs. Upon LIN7A over-expression, we observed hyperproliferation, invasion and a complete absence of lumen formation, revealing strong polarity defects. CONCLUSION: This study therefore shows that LIN7A has a crucial role in the polarity abnormalities associated with breast carcinogenesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13058-016-0680-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-47565022016-02-18 LIN7A is a major determinant of cell-polarity defects in breast carcinomas Gruel, Nadège Fuhrmann, Laetitia Lodillinsky, Catalina Benhamo, Vanessa Mariani, Odette Cédenot, Aurélie Arnould, Laurent Macgrogan, Gaëtan Sastre-Garau, Xavier Chavrier, Philippe Delattre, Olivier Vincent-Salomon, Anne Breast Cancer Res Research Article BACKGROUND: Polarity defects are a hallmark of most carcinomas. Cells from invasive micropapillary carcinomas (IMPCs) of the breast are characterized by a striking cell polarity inversion and represent an interesting model for the analysis of polarity abnormalities. METHODS: In-depth investigation of polarity proteins in 24 IMPCs and a gene expression profiling, comparing IMPC (n = 73) with invasive carcinomas of no special type (ICNST) (n = 51) have been performed. RESULTS: IMPCs showed a profound disorganization of the investigated polarity proteins and revealed major abnormalities in their subcellular localization. Gene expression profiling experiments highlighted a number of deregulated genes in the IMPCs that have a role in apico-basal polarity, adhesion and migration. LIN7A, a Crumbs-complex polarity gene, was one of the most differentially over-expressed genes in the IMPCs. Upon LIN7A over-expression, we observed hyperproliferation, invasion and a complete absence of lumen formation, revealing strong polarity defects. CONCLUSION: This study therefore shows that LIN7A has a crucial role in the polarity abnormalities associated with breast carcinogenesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13058-016-0680-x) contains supplementary material, which is available to authorized users. BioMed Central 2016-02-17 2016 /pmc/articles/PMC4756502/ /pubmed/26887652 http://dx.doi.org/10.1186/s13058-016-0680-x Text en © Gruel et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Gruel, Nadège
Fuhrmann, Laetitia
Lodillinsky, Catalina
Benhamo, Vanessa
Mariani, Odette
Cédenot, Aurélie
Arnould, Laurent
Macgrogan, Gaëtan
Sastre-Garau, Xavier
Chavrier, Philippe
Delattre, Olivier
Vincent-Salomon, Anne
LIN7A is a major determinant of cell-polarity defects in breast carcinomas
title LIN7A is a major determinant of cell-polarity defects in breast carcinomas
title_full LIN7A is a major determinant of cell-polarity defects in breast carcinomas
title_fullStr LIN7A is a major determinant of cell-polarity defects in breast carcinomas
title_full_unstemmed LIN7A is a major determinant of cell-polarity defects in breast carcinomas
title_short LIN7A is a major determinant of cell-polarity defects in breast carcinomas
title_sort lin7a is a major determinant of cell-polarity defects in breast carcinomas
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756502/
https://www.ncbi.nlm.nih.gov/pubmed/26887652
http://dx.doi.org/10.1186/s13058-016-0680-x
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