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Correlation of signal transducer and activator of transcription-3 and β-catenin expression in laryngeal squamous cell carcinoma
OBJECTIVE: The specific roles of phosphorylated signal transducer and activator of transcription-3 (p-STAT3) and β-Catenin in laryngeal squamous cell carcinoma (LSCC) remain unclear. METHODS: In this study, the correlations between p-STAT3, β-Catenin, and clinicopathological characteristics were inv...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107985/ https://www.ncbi.nlm.nih.gov/pubmed/37032609 http://dx.doi.org/10.1177/03000605231166228 |
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author | Sun, Yajing Lu, Xiuying Li, Hui Li, Xiaoming |
author_facet | Sun, Yajing Lu, Xiuying Li, Hui Li, Xiaoming |
author_sort | Sun, Yajing |
collection | PubMed |
description | OBJECTIVE: The specific roles of phosphorylated signal transducer and activator of transcription-3 (p-STAT3) and β-Catenin in laryngeal squamous cell carcinoma (LSCC) remain unclear. METHODS: In this study, the correlations between p-STAT3, β-Catenin, and clinicopathological characteristics were investigated using tissues and clinical data from 124 LSCC cases. Immunohistochemistry and immunofluorescence assays were used to examine p-STAT3 and β-Catenin expression and localization in these samples. Kaplan–Meier survival and Cox regression analyses were performed to evaluate the prognostic significance of these proteins. LSCC cell lines were treated with a STAT3 inhibitor (dihydroartemisinin) or activator (interleukin-6) to explore the mechanism of p-STAT3 and β-Catenin. RESULTS: There was an inverse correlation between p-STAT3 and β-Catenin expression in the LSCC samples. Patients with high p-STAT3 and low β-Catenin expression levels had significantly worse overall survival. Multivariate Cox regression analysis revealed that lymph node metastasis and β-Catenin expression were both independently correlated with unfavorable overall survival. Cell treatment with the p-STAT3 inhibitor inhibited the nuclear accumulation of β-Catenin, while p-STAT3 activator treatment could promote β-Catenin translocation to the nucleus. CONCLUSION: Overall, our data indicate that p-STAT3 expression is associated with LSCC by promoting β-Catenin degradation. |
format | Online Article Text |
id | pubmed-10107985 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-101079852023-04-18 Correlation of signal transducer and activator of transcription-3 and β-catenin expression in laryngeal squamous cell carcinoma Sun, Yajing Lu, Xiuying Li, Hui Li, Xiaoming J Int Med Res Pre-Clinical Research Report OBJECTIVE: The specific roles of phosphorylated signal transducer and activator of transcription-3 (p-STAT3) and β-Catenin in laryngeal squamous cell carcinoma (LSCC) remain unclear. METHODS: In this study, the correlations between p-STAT3, β-Catenin, and clinicopathological characteristics were investigated using tissues and clinical data from 124 LSCC cases. Immunohistochemistry and immunofluorescence assays were used to examine p-STAT3 and β-Catenin expression and localization in these samples. Kaplan–Meier survival and Cox regression analyses were performed to evaluate the prognostic significance of these proteins. LSCC cell lines were treated with a STAT3 inhibitor (dihydroartemisinin) or activator (interleukin-6) to explore the mechanism of p-STAT3 and β-Catenin. RESULTS: There was an inverse correlation between p-STAT3 and β-Catenin expression in the LSCC samples. Patients with high p-STAT3 and low β-Catenin expression levels had significantly worse overall survival. Multivariate Cox regression analysis revealed that lymph node metastasis and β-Catenin expression were both independently correlated with unfavorable overall survival. Cell treatment with the p-STAT3 inhibitor inhibited the nuclear accumulation of β-Catenin, while p-STAT3 activator treatment could promote β-Catenin translocation to the nucleus. CONCLUSION: Overall, our data indicate that p-STAT3 expression is associated with LSCC by promoting β-Catenin degradation. SAGE Publications 2023-04-09 /pmc/articles/PMC10107985/ /pubmed/37032609 http://dx.doi.org/10.1177/03000605231166228 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Pre-Clinical Research Report Sun, Yajing Lu, Xiuying Li, Hui Li, Xiaoming Correlation of signal transducer and activator of transcription-3 and β-catenin expression in laryngeal squamous cell carcinoma |
title | Correlation of signal transducer and activator of transcription-3 and
β-catenin expression in laryngeal squamous cell
carcinoma |
title_full | Correlation of signal transducer and activator of transcription-3 and
β-catenin expression in laryngeal squamous cell
carcinoma |
title_fullStr | Correlation of signal transducer and activator of transcription-3 and
β-catenin expression in laryngeal squamous cell
carcinoma |
title_full_unstemmed | Correlation of signal transducer and activator of transcription-3 and
β-catenin expression in laryngeal squamous cell
carcinoma |
title_short | Correlation of signal transducer and activator of transcription-3 and
β-catenin expression in laryngeal squamous cell
carcinoma |
title_sort | correlation of signal transducer and activator of transcription-3 and
β-catenin expression in laryngeal squamous cell
carcinoma |
topic | Pre-Clinical Research Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107985/ https://www.ncbi.nlm.nih.gov/pubmed/37032609 http://dx.doi.org/10.1177/03000605231166228 |
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