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CDH22 hypermethylation is an independent prognostic biomarker in breast cancer

BACKGROUND: Cadherin-like protein 22 (CDH22) is a transmembrane glycoprotein involved in cell-cell adhesion and metastasis. Its role in cancer is controversial because it has been described as being upregulated in colorectal cancer, whereas it is downregulated in metastatic melanoma. However, its st...

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Autores principales: Martín-Sánchez, Esperanza, Mendaza, Saioa, Ulazia-Garmendia, Ane, Monreal-Santesteban, Iñaki, Córdoba, Alicia, Vicente-García, Francisco, Blanco-Luquin, Idoia, De La Cruz, Susana, Aramendia, Ana, Guerrero-Setas, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5270318/
https://www.ncbi.nlm.nih.gov/pubmed/28149335
http://dx.doi.org/10.1186/s13148-016-0309-z
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author Martín-Sánchez, Esperanza
Mendaza, Saioa
Ulazia-Garmendia, Ane
Monreal-Santesteban, Iñaki
Córdoba, Alicia
Vicente-García, Francisco
Blanco-Luquin, Idoia
De La Cruz, Susana
Aramendia, Ana
Guerrero-Setas, David
author_facet Martín-Sánchez, Esperanza
Mendaza, Saioa
Ulazia-Garmendia, Ane
Monreal-Santesteban, Iñaki
Córdoba, Alicia
Vicente-García, Francisco
Blanco-Luquin, Idoia
De La Cruz, Susana
Aramendia, Ana
Guerrero-Setas, David
author_sort Martín-Sánchez, Esperanza
collection PubMed
description BACKGROUND: Cadherin-like protein 22 (CDH22) is a transmembrane glycoprotein involved in cell-cell adhesion and metastasis. Its role in cancer is controversial because it has been described as being upregulated in colorectal cancer, whereas it is downregulated in metastatic melanoma. However, its status in breast cancer (BC) is unknown. The purpose of our study was to determine the molecular status and clinical value of CDH22 in BC. RESULTS: We observed by immunohistochemistry that the level of CDH22 expression was lower in BC tissues than in their matched adjacent-to-tumour and non-neoplastic tissues from reduction mammoplasties. Since epigenetic alteration is one of the main causes of gene silencing, we analysed the hypermethylation of 3 CpG sites in the CDH22 promoter by pyrosequencing in a series of 142 infiltrating duct BC cases. CDH22 was found to be hypermethylated in tumoral tissues relative to non-neoplastic mammary tissues. Importantly, this epigenetic alteration was already present in adjacent-to-tumour tissues, although to a lesser extent than in tumoral samples. Furthermore, CDH22 gene regulation was dynamically modulated in vitro by epigenetic drugs. Interestingly, CDH22 hypermethylation in all 3 CpG sites simultaneously, but not expression, was significantly associated with shorter progression-free survival (p = 0.015) and overall survival (p = 0.021) in our patient series. Importantly, CDH22 hypermethylation was an independent factor that predicts poor progression-free survival regardless of age and stage (p = 0.006). CONCLUSIONS: Our results are the first evidence that CDH22 is hypermethylated in BC and that this alteration is an independent prognostic factor in BC. Thus, CDH22 hypermethylation could be a potential biomarker of poor prognosis in BC. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13148-016-0309-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-52703182017-02-01 CDH22 hypermethylation is an independent prognostic biomarker in breast cancer Martín-Sánchez, Esperanza Mendaza, Saioa Ulazia-Garmendia, Ane Monreal-Santesteban, Iñaki Córdoba, Alicia Vicente-García, Francisco Blanco-Luquin, Idoia De La Cruz, Susana Aramendia, Ana Guerrero-Setas, David Clin Epigenetics Research BACKGROUND: Cadherin-like protein 22 (CDH22) is a transmembrane glycoprotein involved in cell-cell adhesion and metastasis. Its role in cancer is controversial because it has been described as being upregulated in colorectal cancer, whereas it is downregulated in metastatic melanoma. However, its status in breast cancer (BC) is unknown. The purpose of our study was to determine the molecular status and clinical value of CDH22 in BC. RESULTS: We observed by immunohistochemistry that the level of CDH22 expression was lower in BC tissues than in their matched adjacent-to-tumour and non-neoplastic tissues from reduction mammoplasties. Since epigenetic alteration is one of the main causes of gene silencing, we analysed the hypermethylation of 3 CpG sites in the CDH22 promoter by pyrosequencing in a series of 142 infiltrating duct BC cases. CDH22 was found to be hypermethylated in tumoral tissues relative to non-neoplastic mammary tissues. Importantly, this epigenetic alteration was already present in adjacent-to-tumour tissues, although to a lesser extent than in tumoral samples. Furthermore, CDH22 gene regulation was dynamically modulated in vitro by epigenetic drugs. Interestingly, CDH22 hypermethylation in all 3 CpG sites simultaneously, but not expression, was significantly associated with shorter progression-free survival (p = 0.015) and overall survival (p = 0.021) in our patient series. Importantly, CDH22 hypermethylation was an independent factor that predicts poor progression-free survival regardless of age and stage (p = 0.006). CONCLUSIONS: Our results are the first evidence that CDH22 is hypermethylated in BC and that this alteration is an independent prognostic factor in BC. Thus, CDH22 hypermethylation could be a potential biomarker of poor prognosis in BC. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13148-016-0309-z) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-24 /pmc/articles/PMC5270318/ /pubmed/28149335 http://dx.doi.org/10.1186/s13148-016-0309-z Text en © The Author(s). 2017 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
Martín-Sánchez, Esperanza
Mendaza, Saioa
Ulazia-Garmendia, Ane
Monreal-Santesteban, Iñaki
Córdoba, Alicia
Vicente-García, Francisco
Blanco-Luquin, Idoia
De La Cruz, Susana
Aramendia, Ana
Guerrero-Setas, David
CDH22 hypermethylation is an independent prognostic biomarker in breast cancer
title CDH22 hypermethylation is an independent prognostic biomarker in breast cancer
title_full CDH22 hypermethylation is an independent prognostic biomarker in breast cancer
title_fullStr CDH22 hypermethylation is an independent prognostic biomarker in breast cancer
title_full_unstemmed CDH22 hypermethylation is an independent prognostic biomarker in breast cancer
title_short CDH22 hypermethylation is an independent prognostic biomarker in breast cancer
title_sort cdh22 hypermethylation is an independent prognostic biomarker in breast cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5270318/
https://www.ncbi.nlm.nih.gov/pubmed/28149335
http://dx.doi.org/10.1186/s13148-016-0309-z
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