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Generation and Characterisation of a Canine EGFP-HMGA2 Prostate Cancer In Vitro Model

The architectural transcription factor HMGA2 is abundantly expressed during embryonic development. In several malignant neoplasias including prostate cancer, high re-expression of HMGA2 is correlated with malignancy and poor prognosis. The let-7 miRNA family is described to regulate HMGA2 negatively...

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Autores principales: Willenbrock, Saskia, Wagner, Siegfried, Reimann-Berg, Nicola, Moulay, Mohammed, Hewicker-Trautwein, Marion, Nolte, Ingo, Escobar, Hugo Murua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051699/
https://www.ncbi.nlm.nih.gov/pubmed/24914948
http://dx.doi.org/10.1371/journal.pone.0098788
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author Willenbrock, Saskia
Wagner, Siegfried
Reimann-Berg, Nicola
Moulay, Mohammed
Hewicker-Trautwein, Marion
Nolte, Ingo
Escobar, Hugo Murua
author_facet Willenbrock, Saskia
Wagner, Siegfried
Reimann-Berg, Nicola
Moulay, Mohammed
Hewicker-Trautwein, Marion
Nolte, Ingo
Escobar, Hugo Murua
author_sort Willenbrock, Saskia
collection PubMed
description The architectural transcription factor HMGA2 is abundantly expressed during embryonic development. In several malignant neoplasias including prostate cancer, high re-expression of HMGA2 is correlated with malignancy and poor prognosis. The let-7 miRNA family is described to regulate HMGA2 negatively. The balance of let-7 and HMGA2 is discussed to play a major role in tumour aetiology. To further analyse the role of HMGA2 in prostate cancer a stable and highly reproducible in vitro model system is precondition. Herein we established a canine CT1258-EGFP-HMGA2 prostate cancer cell line stably overexpressing HMGA2 linked to EGFP and in addition the reference cell line CT1258-EGFP expressing solely EGFP to exclude EGFP-induced effects. Both recombinant cell lines were characterised by fluorescence microscopy, flow cytometry and immunocytochemistry. The proliferative effect of ectopically overexpressed HMGA2 was determined via BrdU assays. Comparative karyotyping of the derived and the initial CT1258 cell lines was performed to analyse chromosome consistency. The impact of the ectopic HMGA2 expression on its regulator let-7a was analysed by quantitative real-time PCR. Fluorescence microscopy and immunocytochemistry detected successful expression of the EGFP-HMGA2 fusion protein exclusively accumulating in the nucleus. Gene expression analyses confirmed HMGA2 overexpression in CT1258-EGFP-HMGA2 in comparison to CT1258-EGFP and native cells. Significantly higher let-7a expression levels were found in CT1258-EGFP-HMGA2 and CT1258-EGFP. The BrdU assays detected an increased proliferation of CT1258-HMGA2-EGFP cells compared to CT1258-EGFP and native CT1258. The cytogenetic analyses of CT1258-EGFP and CT1258-EGFP-HMGA2 resulted in a comparable hyperdiploid karyotype as described for native CT1258 cells. To further investigate the impact of recombinant overexpressed HMGA2 on CT1258 cells, other selected targets described to underlie HMGA2 regulation were screened in addition. The new fluorescent CT1258-EGFP-HMGA2 cell line is a stable tool enabling in vitro and in vivo analyses of the HMGA2-mediated effects on cells and the development and pathogenesis of prostate cancer.
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spelling pubmed-40516992014-06-18 Generation and Characterisation of a Canine EGFP-HMGA2 Prostate Cancer In Vitro Model Willenbrock, Saskia Wagner, Siegfried Reimann-Berg, Nicola Moulay, Mohammed Hewicker-Trautwein, Marion Nolte, Ingo Escobar, Hugo Murua PLoS One Research Article The architectural transcription factor HMGA2 is abundantly expressed during embryonic development. In several malignant neoplasias including prostate cancer, high re-expression of HMGA2 is correlated with malignancy and poor prognosis. The let-7 miRNA family is described to regulate HMGA2 negatively. The balance of let-7 and HMGA2 is discussed to play a major role in tumour aetiology. To further analyse the role of HMGA2 in prostate cancer a stable and highly reproducible in vitro model system is precondition. Herein we established a canine CT1258-EGFP-HMGA2 prostate cancer cell line stably overexpressing HMGA2 linked to EGFP and in addition the reference cell line CT1258-EGFP expressing solely EGFP to exclude EGFP-induced effects. Both recombinant cell lines were characterised by fluorescence microscopy, flow cytometry and immunocytochemistry. The proliferative effect of ectopically overexpressed HMGA2 was determined via BrdU assays. Comparative karyotyping of the derived and the initial CT1258 cell lines was performed to analyse chromosome consistency. The impact of the ectopic HMGA2 expression on its regulator let-7a was analysed by quantitative real-time PCR. Fluorescence microscopy and immunocytochemistry detected successful expression of the EGFP-HMGA2 fusion protein exclusively accumulating in the nucleus. Gene expression analyses confirmed HMGA2 overexpression in CT1258-EGFP-HMGA2 in comparison to CT1258-EGFP and native cells. Significantly higher let-7a expression levels were found in CT1258-EGFP-HMGA2 and CT1258-EGFP. The BrdU assays detected an increased proliferation of CT1258-HMGA2-EGFP cells compared to CT1258-EGFP and native CT1258. The cytogenetic analyses of CT1258-EGFP and CT1258-EGFP-HMGA2 resulted in a comparable hyperdiploid karyotype as described for native CT1258 cells. To further investigate the impact of recombinant overexpressed HMGA2 on CT1258 cells, other selected targets described to underlie HMGA2 regulation were screened in addition. The new fluorescent CT1258-EGFP-HMGA2 cell line is a stable tool enabling in vitro and in vivo analyses of the HMGA2-mediated effects on cells and the development and pathogenesis of prostate cancer. Public Library of Science 2014-06-10 /pmc/articles/PMC4051699/ /pubmed/24914948 http://dx.doi.org/10.1371/journal.pone.0098788 Text en © 2014 Willenbrock 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
Willenbrock, Saskia
Wagner, Siegfried
Reimann-Berg, Nicola
Moulay, Mohammed
Hewicker-Trautwein, Marion
Nolte, Ingo
Escobar, Hugo Murua
Generation and Characterisation of a Canine EGFP-HMGA2 Prostate Cancer In Vitro Model
title Generation and Characterisation of a Canine EGFP-HMGA2 Prostate Cancer In Vitro Model
title_full Generation and Characterisation of a Canine EGFP-HMGA2 Prostate Cancer In Vitro Model
title_fullStr Generation and Characterisation of a Canine EGFP-HMGA2 Prostate Cancer In Vitro Model
title_full_unstemmed Generation and Characterisation of a Canine EGFP-HMGA2 Prostate Cancer In Vitro Model
title_short Generation and Characterisation of a Canine EGFP-HMGA2 Prostate Cancer In Vitro Model
title_sort generation and characterisation of a canine egfp-hmga2 prostate cancer in vitro model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051699/
https://www.ncbi.nlm.nih.gov/pubmed/24914948
http://dx.doi.org/10.1371/journal.pone.0098788
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