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HMGA1 and HMGA2 expression and comparative analyses of HMGA2, Lin28 and let-7 miRNAs in oral squamous cell carcinoma

BACKGROUND: Humans and dogs are affected by squamous cell carcinomas of the oral cavity (OSCC) in a considerably high frequency. The high mobility group A2 (HMGA2) protein was found to be highly expressed in human OSCC and its expression was suggested to act as a useful predictive and prognostic too...

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Autores principales: Sterenczak, Katharina Anna, Eckardt, Andre, Kampmann, Andreas, Willenbrock, Saskia, Eberle, Nina, Länger, Florian, Kleinschmidt, Sven, Hewicker-Trautwein, Marion, Kreipe, Hans, Nolte, Ingo, Escobar, Hugo Murua, Gellrich, Nils Claudius
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190370/
https://www.ncbi.nlm.nih.gov/pubmed/25245141
http://dx.doi.org/10.1186/1471-2407-14-694
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author Sterenczak, Katharina Anna
Eckardt, Andre
Kampmann, Andreas
Willenbrock, Saskia
Eberle, Nina
Länger, Florian
Kleinschmidt, Sven
Hewicker-Trautwein, Marion
Kreipe, Hans
Nolte, Ingo
Escobar, Hugo Murua
Gellrich, Nils Claudius
author_facet Sterenczak, Katharina Anna
Eckardt, Andre
Kampmann, Andreas
Willenbrock, Saskia
Eberle, Nina
Länger, Florian
Kleinschmidt, Sven
Hewicker-Trautwein, Marion
Kreipe, Hans
Nolte, Ingo
Escobar, Hugo Murua
Gellrich, Nils Claudius
author_sort Sterenczak, Katharina Anna
collection PubMed
description BACKGROUND: Humans and dogs are affected by squamous cell carcinomas of the oral cavity (OSCC) in a considerably high frequency. The high mobility group A2 (HMGA2) protein was found to be highly expressed in human OSCC and its expression was suggested to act as a useful predictive and prognostic tool in clinical management of oral carcinomas. Herein the expression of HMGA2 and its sister gene HMGA1 were analysed within human and canine OSCC samples. Additionally, the HMGA negatively regulating miRNAs of the let-7 family as well as the let-7 regulating gene Lin28 were also comparatively analysed. Deregulations of either one of these members could affect the progression of human and canine OSCC. METHODS: Expression levels of HMGA1, HMGA2, Lin28, let-7a and mir-98 were analysed via relative qPCR in primary human and canine OSCC, thereof derived cell lines and non-neoplastic samples. Additionally, comparative HMGA2 protein expression was analysed by immunohistochemistry. RESULTS: In both species, a significant up-regulation of the HMGA2 gene was found within the neoplastic samples while HMGA1 expression did not show significant deregulations. Comparative analyses showed down-regulation of mir-98 in human samples and up-regulation of let-7a and mir-98 in canine neoplastic samples. HMGA2 immunostainings showed higher intensities within the invasive front of the tumours than in the centre of the tumour in both species. CONCLUSIONS: HMGA2 could potentially serve as tumour marker in both species while HMGA1 might play a minor role in OSCC progression. Comparative studies indicate an inverse correlation of HMGA2 and mir-98 expression in human samples whereas in dogs no such characteristic could be found. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2407-14-694) contains supplementary material, which is available to authorized users.
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spelling pubmed-41903702014-10-10 HMGA1 and HMGA2 expression and comparative analyses of HMGA2, Lin28 and let-7 miRNAs in oral squamous cell carcinoma Sterenczak, Katharina Anna Eckardt, Andre Kampmann, Andreas Willenbrock, Saskia Eberle, Nina Länger, Florian Kleinschmidt, Sven Hewicker-Trautwein, Marion Kreipe, Hans Nolte, Ingo Escobar, Hugo Murua Gellrich, Nils Claudius BMC Cancer Research Article BACKGROUND: Humans and dogs are affected by squamous cell carcinomas of the oral cavity (OSCC) in a considerably high frequency. The high mobility group A2 (HMGA2) protein was found to be highly expressed in human OSCC and its expression was suggested to act as a useful predictive and prognostic tool in clinical management of oral carcinomas. Herein the expression of HMGA2 and its sister gene HMGA1 were analysed within human and canine OSCC samples. Additionally, the HMGA negatively regulating miRNAs of the let-7 family as well as the let-7 regulating gene Lin28 were also comparatively analysed. Deregulations of either one of these members could affect the progression of human and canine OSCC. METHODS: Expression levels of HMGA1, HMGA2, Lin28, let-7a and mir-98 were analysed via relative qPCR in primary human and canine OSCC, thereof derived cell lines and non-neoplastic samples. Additionally, comparative HMGA2 protein expression was analysed by immunohistochemistry. RESULTS: In both species, a significant up-regulation of the HMGA2 gene was found within the neoplastic samples while HMGA1 expression did not show significant deregulations. Comparative analyses showed down-regulation of mir-98 in human samples and up-regulation of let-7a and mir-98 in canine neoplastic samples. HMGA2 immunostainings showed higher intensities within the invasive front of the tumours than in the centre of the tumour in both species. CONCLUSIONS: HMGA2 could potentially serve as tumour marker in both species while HMGA1 might play a minor role in OSCC progression. Comparative studies indicate an inverse correlation of HMGA2 and mir-98 expression in human samples whereas in dogs no such characteristic could be found. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2407-14-694) contains supplementary material, which is available to authorized users. BioMed Central 2014-09-23 /pmc/articles/PMC4190370/ /pubmed/25245141 http://dx.doi.org/10.1186/1471-2407-14-694 Text en © Sterenczak et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Sterenczak, Katharina Anna
Eckardt, Andre
Kampmann, Andreas
Willenbrock, Saskia
Eberle, Nina
Länger, Florian
Kleinschmidt, Sven
Hewicker-Trautwein, Marion
Kreipe, Hans
Nolte, Ingo
Escobar, Hugo Murua
Gellrich, Nils Claudius
HMGA1 and HMGA2 expression and comparative analyses of HMGA2, Lin28 and let-7 miRNAs in oral squamous cell carcinoma
title HMGA1 and HMGA2 expression and comparative analyses of HMGA2, Lin28 and let-7 miRNAs in oral squamous cell carcinoma
title_full HMGA1 and HMGA2 expression and comparative analyses of HMGA2, Lin28 and let-7 miRNAs in oral squamous cell carcinoma
title_fullStr HMGA1 and HMGA2 expression and comparative analyses of HMGA2, Lin28 and let-7 miRNAs in oral squamous cell carcinoma
title_full_unstemmed HMGA1 and HMGA2 expression and comparative analyses of HMGA2, Lin28 and let-7 miRNAs in oral squamous cell carcinoma
title_short HMGA1 and HMGA2 expression and comparative analyses of HMGA2, Lin28 and let-7 miRNAs in oral squamous cell carcinoma
title_sort hmga1 and hmga2 expression and comparative analyses of hmga2, lin28 and let-7 mirnas in oral squamous cell carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190370/
https://www.ncbi.nlm.nih.gov/pubmed/25245141
http://dx.doi.org/10.1186/1471-2407-14-694
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