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AP-2α expression in papillary thyroid carcinoma predicts tumor progression and poor prognosis

BACKGROUND: The activator protein (AP)-2α is involved in a wide variety of biologic processes in tumor. However, little is known about the role of AP-2α in human papillary thyroid carcinoma (PTC). METHODS: The immunohistochemical method was used to detect AP-2α expression in 63 PTC cases. Western bl...

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Autores principales: Wu, Hong Rong, Zhang, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6095110/
https://www.ncbi.nlm.nih.gov/pubmed/30147362
http://dx.doi.org/10.2147/CMAR.S167874
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author Wu, Hong Rong
Zhang, Jian
author_facet Wu, Hong Rong
Zhang, Jian
author_sort Wu, Hong Rong
collection PubMed
description BACKGROUND: The activator protein (AP)-2α is involved in a wide variety of biologic processes in tumor. However, little is known about the role of AP-2α in human papillary thyroid carcinoma (PTC). METHODS: The immunohistochemical method was used to detect AP-2α expression in 63 PTC cases. Western blotting was carried out to assess the change in expression of certain proteins. The bioinformatics analysis of 496 PTC samples comes from The Cancer Genome Atlas (TCGA). The Gene Set Enrichment Analysis (GSEA) was performed using TCGA data set. Cell transfection was used to induce related protein expression or to repress it by RNA interference procedures. RESULTS: Our results demonstrated that AP-2α expression was higher in tumor tissues than the corresponding adjacent nontumor tissues, the positive substances of AP-2α were observed mainly in the cytoplasm of PTC, and AP-2α was positively correlated with histologic type (P=0.026) of PTC patients. The high expression of AP-2α mRNA was associated significantly with tumor stages (P=0.011), histologic type (P=0.019), and independently predicted shorter overall survival (P=0.005) based on TCGA analysis. Patients with high AP-2α mRNA expression have shorter overall survival compared to those with low AP-2α mRNA expression, particularly in advanced tumor stages (III and IV) of PTC patients (P=0.011). Multivariate analysis suggested that AP-2α mRNA expression might be an independent prognostic indicator for the survival of patients with PTC (P=0.037). Moreover, the association between enhanced AP-2α expression and two pathways (notch signaling and focal adhesion) was revealed by GSEA, and then confirmed by cellular experiments. CONCLUSION: Taken together, our findings suggest that AP-2α may be a potential prognostic molecular marker and therapeutic target for PTC patients.
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spelling pubmed-60951102018-08-24 AP-2α expression in papillary thyroid carcinoma predicts tumor progression and poor prognosis Wu, Hong Rong Zhang, Jian Cancer Manag Res Original Research BACKGROUND: The activator protein (AP)-2α is involved in a wide variety of biologic processes in tumor. However, little is known about the role of AP-2α in human papillary thyroid carcinoma (PTC). METHODS: The immunohistochemical method was used to detect AP-2α expression in 63 PTC cases. Western blotting was carried out to assess the change in expression of certain proteins. The bioinformatics analysis of 496 PTC samples comes from The Cancer Genome Atlas (TCGA). The Gene Set Enrichment Analysis (GSEA) was performed using TCGA data set. Cell transfection was used to induce related protein expression or to repress it by RNA interference procedures. RESULTS: Our results demonstrated that AP-2α expression was higher in tumor tissues than the corresponding adjacent nontumor tissues, the positive substances of AP-2α were observed mainly in the cytoplasm of PTC, and AP-2α was positively correlated with histologic type (P=0.026) of PTC patients. The high expression of AP-2α mRNA was associated significantly with tumor stages (P=0.011), histologic type (P=0.019), and independently predicted shorter overall survival (P=0.005) based on TCGA analysis. Patients with high AP-2α mRNA expression have shorter overall survival compared to those with low AP-2α mRNA expression, particularly in advanced tumor stages (III and IV) of PTC patients (P=0.011). Multivariate analysis suggested that AP-2α mRNA expression might be an independent prognostic indicator for the survival of patients with PTC (P=0.037). Moreover, the association between enhanced AP-2α expression and two pathways (notch signaling and focal adhesion) was revealed by GSEA, and then confirmed by cellular experiments. CONCLUSION: Taken together, our findings suggest that AP-2α may be a potential prognostic molecular marker and therapeutic target for PTC patients. Dove Medical Press 2018-08-13 /pmc/articles/PMC6095110/ /pubmed/30147362 http://dx.doi.org/10.2147/CMAR.S167874 Text en © 2018 Wu and Zhang. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Wu, Hong Rong
Zhang, Jian
AP-2α expression in papillary thyroid carcinoma predicts tumor progression and poor prognosis
title AP-2α expression in papillary thyroid carcinoma predicts tumor progression and poor prognosis
title_full AP-2α expression in papillary thyroid carcinoma predicts tumor progression and poor prognosis
title_fullStr AP-2α expression in papillary thyroid carcinoma predicts tumor progression and poor prognosis
title_full_unstemmed AP-2α expression in papillary thyroid carcinoma predicts tumor progression and poor prognosis
title_short AP-2α expression in papillary thyroid carcinoma predicts tumor progression and poor prognosis
title_sort ap-2α expression in papillary thyroid carcinoma predicts tumor progression and poor prognosis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6095110/
https://www.ncbi.nlm.nih.gov/pubmed/30147362
http://dx.doi.org/10.2147/CMAR.S167874
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