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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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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. |
format | Online Article Text |
id | pubmed-4756502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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