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Expression of yes-associated protein, β-catenin and smoothened, and their clinical significance in invasive breast cancer

The expression profile and role of yes-associated protein (YAP) in occurrence and development of breast cancer is ambiguous. The present study aimed to explore the relationship among the YAP, β-catenin and smoothened (SMO) signaling pathways to provide a theoretical basis for the clinical diagnosis...

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Autores principales: Liu, Pengju, Zeng, Jianfeng, Yang, Gaohua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9121206/
https://www.ncbi.nlm.nih.gov/pubmed/35607374
http://dx.doi.org/10.3892/etm.2022.11356
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author Liu, Pengju
Zeng, Jianfeng
Yang, Gaohua
author_facet Liu, Pengju
Zeng, Jianfeng
Yang, Gaohua
author_sort Liu, Pengju
collection PubMed
description The expression profile and role of yes-associated protein (YAP) in occurrence and development of breast cancer is ambiguous. The present study aimed to explore the relationship among the YAP, β-catenin and smoothened (SMO) signaling pathways to provide a theoretical basis for the clinical diagnosis and treatment of invasive breast cancer. Immunohistochemistry was used to determine the protein expression levels of YAP, β-catenin and SMO in tumor, tumor-adjacent and normal breast tissue. The possible association between the expression levels of these three proteins and the clinicopathological features of patients with breast cancer was then analyzed by the χ(2) test. The protein expression of YAP was found to be downregulated, whilst β-catenin and SMO expression were found to be upregulated in tumor tissues as compared with that in normal breast tissues. In addition, the expression of YAP in breast cancer tissues was found to be associated with that of human epidermal growth factor receptor 2 (HER2), progesterone and estrogen receptors. By contrast, the protein expression of β-catenin and SMO in breast cancer tissues was only associated with HER2. There was a negative correlation between the expression of YAP and SMO protein in breast cancer tissues. Compared with that in the changes in each of YAP, β-catenin and SMO protein expression levels individually, their combined changes in expression were demonstrated to associate significantly with the tumor histological grade. To conclude, data from the present study suggest that the combined protein expression of YAP, β-catenin and SMO can be used as a prognostic indicator for the treatment of invasive breast cancer.
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spelling pubmed-91212062022-05-22 Expression of yes-associated protein, β-catenin and smoothened, and their clinical significance in invasive breast cancer Liu, Pengju Zeng, Jianfeng Yang, Gaohua Exp Ther Med Articles The expression profile and role of yes-associated protein (YAP) in occurrence and development of breast cancer is ambiguous. The present study aimed to explore the relationship among the YAP, β-catenin and smoothened (SMO) signaling pathways to provide a theoretical basis for the clinical diagnosis and treatment of invasive breast cancer. Immunohistochemistry was used to determine the protein expression levels of YAP, β-catenin and SMO in tumor, tumor-adjacent and normal breast tissue. The possible association between the expression levels of these three proteins and the clinicopathological features of patients with breast cancer was then analyzed by the χ(2) test. The protein expression of YAP was found to be downregulated, whilst β-catenin and SMO expression were found to be upregulated in tumor tissues as compared with that in normal breast tissues. In addition, the expression of YAP in breast cancer tissues was found to be associated with that of human epidermal growth factor receptor 2 (HER2), progesterone and estrogen receptors. By contrast, the protein expression of β-catenin and SMO in breast cancer tissues was only associated with HER2. There was a negative correlation between the expression of YAP and SMO protein in breast cancer tissues. Compared with that in the changes in each of YAP, β-catenin and SMO protein expression levels individually, their combined changes in expression were demonstrated to associate significantly with the tumor histological grade. To conclude, data from the present study suggest that the combined protein expression of YAP, β-catenin and SMO can be used as a prognostic indicator for the treatment of invasive breast cancer. D.A. Spandidos 2022-06 2022-05-06 /pmc/articles/PMC9121206/ /pubmed/35607374 http://dx.doi.org/10.3892/etm.2022.11356 Text en Copyright: © Liu et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Liu, Pengju
Zeng, Jianfeng
Yang, Gaohua
Expression of yes-associated protein, β-catenin and smoothened, and their clinical significance in invasive breast cancer
title Expression of yes-associated protein, β-catenin and smoothened, and their clinical significance in invasive breast cancer
title_full Expression of yes-associated protein, β-catenin and smoothened, and their clinical significance in invasive breast cancer
title_fullStr Expression of yes-associated protein, β-catenin and smoothened, and their clinical significance in invasive breast cancer
title_full_unstemmed Expression of yes-associated protein, β-catenin and smoothened, and their clinical significance in invasive breast cancer
title_short Expression of yes-associated protein, β-catenin and smoothened, and their clinical significance in invasive breast cancer
title_sort expression of yes-associated protein, β-catenin and smoothened, and their clinical significance in invasive breast cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9121206/
https://www.ncbi.nlm.nih.gov/pubmed/35607374
http://dx.doi.org/10.3892/etm.2022.11356
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