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MiR-21 Expression in the Tumor Stroma of Oral Squamous Cell Carcinoma: An Independent Biomarker of Disease Free Survival

Oral squamous cell carcinoma (OSCC) patients have a high mortality rate; thus, new clinical biomarkers and therapeutic options are needed. MicroRNAs (miRNAs) are short noncoding RNAs that regulate posttranscriptional gene expression and are commonly deregulated in OSCC and other cancers. MicroRNA-21...

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Autores principales: Hedbäck, Nora, Jensen, David H., Specht, Lena, Fiehn, Anne-Marie K., Therkildsen, Marianne H., Friis-Hansen, Lennart, Dabelsteen, Erik, von Buchwald, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995812/
https://www.ncbi.nlm.nih.gov/pubmed/24755828
http://dx.doi.org/10.1371/journal.pone.0095193
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author Hedbäck, Nora
Jensen, David H.
Specht, Lena
Fiehn, Anne-Marie K.
Therkildsen, Marianne H.
Friis-Hansen, Lennart
Dabelsteen, Erik
von Buchwald, Christian
author_facet Hedbäck, Nora
Jensen, David H.
Specht, Lena
Fiehn, Anne-Marie K.
Therkildsen, Marianne H.
Friis-Hansen, Lennart
Dabelsteen, Erik
von Buchwald, Christian
author_sort Hedbäck, Nora
collection PubMed
description Oral squamous cell carcinoma (OSCC) patients have a high mortality rate; thus, new clinical biomarkers and therapeutic options are needed. MicroRNAs (miRNAs) are short noncoding RNAs that regulate posttranscriptional gene expression and are commonly deregulated in OSCC and other cancers. MicroRNA-21 (miR-21) is the most consistently overexpressed miRNA in several types of cancer, and it might be a useful clinical biomarker and therapeutic target. To better understand the role of miR-21 in OSCC, paraffin-embedded tumor tissue samples from 86 patients with primary OSCC were analyzed by in situ hybridization. We found that miR-21 was primarily expressed in the tumor stroma and in some tumor-associated blood vessels with no expression in the adjacent normal epithelia or stroma. Using image analysis, we quantitatively estimated miR-21 expression levels specifically in the stroma of a cohort of OSCC samples. These miR-21 levels significantly correlated with disease free survival with the highest levels being located in the stroma. Stromal miR-21 expression was independently associated with a poorer prognosis, even after adjusting for clinical parameters (perineural invasion and N-stage) in a multivariate analysis. In summary, we have shown that miR-21 is located in the carcinoma cells, stroma and blood vessels of tumors, and its expression specifically in the stromal compartment has a negative prognostic value in OSCC.
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spelling pubmed-39958122014-04-25 MiR-21 Expression in the Tumor Stroma of Oral Squamous Cell Carcinoma: An Independent Biomarker of Disease Free Survival Hedbäck, Nora Jensen, David H. Specht, Lena Fiehn, Anne-Marie K. Therkildsen, Marianne H. Friis-Hansen, Lennart Dabelsteen, Erik von Buchwald, Christian PLoS One Research Article Oral squamous cell carcinoma (OSCC) patients have a high mortality rate; thus, new clinical biomarkers and therapeutic options are needed. MicroRNAs (miRNAs) are short noncoding RNAs that regulate posttranscriptional gene expression and are commonly deregulated in OSCC and other cancers. MicroRNA-21 (miR-21) is the most consistently overexpressed miRNA in several types of cancer, and it might be a useful clinical biomarker and therapeutic target. To better understand the role of miR-21 in OSCC, paraffin-embedded tumor tissue samples from 86 patients with primary OSCC were analyzed by in situ hybridization. We found that miR-21 was primarily expressed in the tumor stroma and in some tumor-associated blood vessels with no expression in the adjacent normal epithelia or stroma. Using image analysis, we quantitatively estimated miR-21 expression levels specifically in the stroma of a cohort of OSCC samples. These miR-21 levels significantly correlated with disease free survival with the highest levels being located in the stroma. Stromal miR-21 expression was independently associated with a poorer prognosis, even after adjusting for clinical parameters (perineural invasion and N-stage) in a multivariate analysis. In summary, we have shown that miR-21 is located in the carcinoma cells, stroma and blood vessels of tumors, and its expression specifically in the stromal compartment has a negative prognostic value in OSCC. Public Library of Science 2014-04-22 /pmc/articles/PMC3995812/ /pubmed/24755828 http://dx.doi.org/10.1371/journal.pone.0095193 Text en © 2014 Hedbäck et al http://creativecommons.org/licenses/by/4.0/ 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 author and source are properly credited.
spellingShingle Research Article
Hedbäck, Nora
Jensen, David H.
Specht, Lena
Fiehn, Anne-Marie K.
Therkildsen, Marianne H.
Friis-Hansen, Lennart
Dabelsteen, Erik
von Buchwald, Christian
MiR-21 Expression in the Tumor Stroma of Oral Squamous Cell Carcinoma: An Independent Biomarker of Disease Free Survival
title MiR-21 Expression in the Tumor Stroma of Oral Squamous Cell Carcinoma: An Independent Biomarker of Disease Free Survival
title_full MiR-21 Expression in the Tumor Stroma of Oral Squamous Cell Carcinoma: An Independent Biomarker of Disease Free Survival
title_fullStr MiR-21 Expression in the Tumor Stroma of Oral Squamous Cell Carcinoma: An Independent Biomarker of Disease Free Survival
title_full_unstemmed MiR-21 Expression in the Tumor Stroma of Oral Squamous Cell Carcinoma: An Independent Biomarker of Disease Free Survival
title_short MiR-21 Expression in the Tumor Stroma of Oral Squamous Cell Carcinoma: An Independent Biomarker of Disease Free Survival
title_sort mir-21 expression in the tumor stroma of oral squamous cell carcinoma: an independent biomarker of disease free survival
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995812/
https://www.ncbi.nlm.nih.gov/pubmed/24755828
http://dx.doi.org/10.1371/journal.pone.0095193
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