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E-Cadherin gene expression in oral cancer: Clinical and prospective data
BACKGROUND: Low protein expression of E-cadherin in oral squamous cell carcinoma (OSCC) has been associated with clinical and histopathological traits such as metastases, recurrence, low survival and poor tumor differentiation, and it is considered a high-risk marker of malignancy. However, it is st...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medicina Oral S.L.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6667017/ https://www.ncbi.nlm.nih.gov/pubmed/31256188 http://dx.doi.org/10.4317/medoral.23029 |
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author | López-Verdín, Sandra Martínez-Fierro, Margarita de la Luz Garza-Veloz, Idalia Zamora-Perez, Ana Grajeda-Cruz, Jonathan González-González, Rogelio Molina-Frechero, Nelly Arocena, Miguel Bologna-Molina, Ronell |
author_facet | López-Verdín, Sandra Martínez-Fierro, Margarita de la Luz Garza-Veloz, Idalia Zamora-Perez, Ana Grajeda-Cruz, Jonathan González-González, Rogelio Molina-Frechero, Nelly Arocena, Miguel Bologna-Molina, Ronell |
author_sort | López-Verdín, Sandra |
collection | PubMed |
description | BACKGROUND: Low protein expression of E-cadherin in oral squamous cell carcinoma (OSCC) has been associated with clinical and histopathological traits such as metastases, recurrence, low survival and poor tumor differentiation, and it is considered a high-risk marker of malignancy. However, it is still unknown whether low expression of E-cadherin is also present at the mRNA level in OSCC cases. Objective: The aim of this study was to compare E-cadherin mRNA expression in OSCC patients and controls and to correlate the expression with clinical and prospective characteristics. MATERIAL AND METHODS: Forty patients and 40 controls were enrolled. E-cadherin mRNA expression was evaluated by quantitative real-time polymerase chain reaction using TaqMan probes. RESULTS: E-cadherin mRNA expression was significantly decreased in OSCC patients compared to that of controls (p<0.001). Whereas no significant association between clinical parameters and E-cadherin expression levels was observed, we noted lower E-cadherin expression levels in patients with positive lymph node metastasis. CONCLUSIONS: E-cadherin mRNA expression was markedly diminished in OSCC, in agreement with previous results that examined E-cadherin expression at the protein level. E-cadherin is downregulated in the early clinical stages of OSCC, and its mRNA levels do not change significantly in the advanced stages, suggesting that there is limited usefulness of this parameter for predicting disease progression. Key words:Oral cancer, E-Cadherin, gene expression. |
format | Online Article Text |
id | pubmed-6667017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Medicina Oral S.L. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66670172019-08-02 E-Cadherin gene expression in oral cancer: Clinical and prospective data López-Verdín, Sandra Martínez-Fierro, Margarita de la Luz Garza-Veloz, Idalia Zamora-Perez, Ana Grajeda-Cruz, Jonathan González-González, Rogelio Molina-Frechero, Nelly Arocena, Miguel Bologna-Molina, Ronell Med Oral Patol Oral Cir Bucal Research BACKGROUND: Low protein expression of E-cadherin in oral squamous cell carcinoma (OSCC) has been associated with clinical and histopathological traits such as metastases, recurrence, low survival and poor tumor differentiation, and it is considered a high-risk marker of malignancy. However, it is still unknown whether low expression of E-cadherin is also present at the mRNA level in OSCC cases. Objective: The aim of this study was to compare E-cadherin mRNA expression in OSCC patients and controls and to correlate the expression with clinical and prospective characteristics. MATERIAL AND METHODS: Forty patients and 40 controls were enrolled. E-cadherin mRNA expression was evaluated by quantitative real-time polymerase chain reaction using TaqMan probes. RESULTS: E-cadherin mRNA expression was significantly decreased in OSCC patients compared to that of controls (p<0.001). Whereas no significant association between clinical parameters and E-cadherin expression levels was observed, we noted lower E-cadherin expression levels in patients with positive lymph node metastasis. CONCLUSIONS: E-cadherin mRNA expression was markedly diminished in OSCC, in agreement with previous results that examined E-cadherin expression at the protein level. E-cadherin is downregulated in the early clinical stages of OSCC, and its mRNA levels do not change significantly in the advanced stages, suggesting that there is limited usefulness of this parameter for predicting disease progression. Key words:Oral cancer, E-Cadherin, gene expression. Medicina Oral S.L. 2019-07 /pmc/articles/PMC6667017/ /pubmed/31256188 http://dx.doi.org/10.4317/medoral.23029 Text en Copyright: © 2019 Medicina Oral S.L. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research López-Verdín, Sandra Martínez-Fierro, Margarita de la Luz Garza-Veloz, Idalia Zamora-Perez, Ana Grajeda-Cruz, Jonathan González-González, Rogelio Molina-Frechero, Nelly Arocena, Miguel Bologna-Molina, Ronell E-Cadherin gene expression in oral cancer: Clinical and prospective data |
title | E-Cadherin gene expression in oral cancer: Clinical and prospective data |
title_full | E-Cadherin gene expression in oral cancer: Clinical and prospective data |
title_fullStr | E-Cadherin gene expression in oral cancer: Clinical and prospective data |
title_full_unstemmed | E-Cadherin gene expression in oral cancer: Clinical and prospective data |
title_short | E-Cadherin gene expression in oral cancer: Clinical and prospective data |
title_sort | e-cadherin gene expression in oral cancer: clinical and prospective data |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6667017/ https://www.ncbi.nlm.nih.gov/pubmed/31256188 http://dx.doi.org/10.4317/medoral.23029 |
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