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High expression of phosphorylated focal adhesion kinase predicts a poor prognosis in human colorectal cancer

Background: Phosphorylated Focal adhesion kinase (FAK) has been reported to be intimately involved in various malignant tumors. The effect of p-FAK on colorectal cancer (CRC) is still disputable. The purpose of this study is to investigate the role of p-FAK in the prognosis of colorectal cancer. Met...

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Autores principales: Yu, Guanyu, Xu, Mengnan, Zhou, Leqi, Zheng, Kuo, Zhu, Xiaoming, Sui, Jinke, Xin, Cheng, Chang, Wenjun, Zhang, Wei, Cao, Fuao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9513477/
https://www.ncbi.nlm.nih.gov/pubmed/36176444
http://dx.doi.org/10.3389/fphar.2022.989999
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author Yu, Guanyu
Xu, Mengnan
Zhou, Leqi
Zheng, Kuo
Zhu, Xiaoming
Sui, Jinke
Xin, Cheng
Chang, Wenjun
Zhang, Wei
Cao, Fuao
author_facet Yu, Guanyu
Xu, Mengnan
Zhou, Leqi
Zheng, Kuo
Zhu, Xiaoming
Sui, Jinke
Xin, Cheng
Chang, Wenjun
Zhang, Wei
Cao, Fuao
author_sort Yu, Guanyu
collection PubMed
description Background: Phosphorylated Focal adhesion kinase (FAK) has been reported to be intimately involved in various malignant tumors. The effect of p-FAK on colorectal cancer (CRC) is still disputable. The purpose of this study is to investigate the role of p-FAK in the prognosis of colorectal cancer. Methods: The clinical significance of p-FAK expression in CRC was evaluated by immunohistochemistry in a large cohort, including carcinoma and para-carcinoma tissues from 908 patients, and normal tissues, adenoma, and metastasis tissues. The correlation between p-FAK expression and CRC occurrence was investigated in tumor and other tissues. Factors contributing to prognosis were evaluated using Kaplan-Meier survival analysis and Cox regression model. Results: p-FAK is apparently overexpressed in CRC and metastasis tissues. Compared with low p-FAK expression, patients with high p-FAK expression had shorter overall survival [hazard ratio (HR), 2.200; 95% confidence interval (CI), 1.265–3.452; p < 0.01] and disease-free survival (HR, 2.004; 95% CI 1.262–3.382; p < 0.01) in multivariate Cox analysis after adjusting other prognostic factors. High p-FAK expression was also related to a worse chemotherapeutic response in patients who achieved adjuvant chemotherapy (p < 0.01). Conclusion: Expression level of p-FAK is an independent risk factor and can serve as a prognostic biomarker for CRC. High p-FAK expression predicts an unfavorable prognosis of CRC as well as poor chemotherapeutic response.
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spelling pubmed-95134772022-09-28 High expression of phosphorylated focal adhesion kinase predicts a poor prognosis in human colorectal cancer Yu, Guanyu Xu, Mengnan Zhou, Leqi Zheng, Kuo Zhu, Xiaoming Sui, Jinke Xin, Cheng Chang, Wenjun Zhang, Wei Cao, Fuao Front Pharmacol Pharmacology Background: Phosphorylated Focal adhesion kinase (FAK) has been reported to be intimately involved in various malignant tumors. The effect of p-FAK on colorectal cancer (CRC) is still disputable. The purpose of this study is to investigate the role of p-FAK in the prognosis of colorectal cancer. Methods: The clinical significance of p-FAK expression in CRC was evaluated by immunohistochemistry in a large cohort, including carcinoma and para-carcinoma tissues from 908 patients, and normal tissues, adenoma, and metastasis tissues. The correlation between p-FAK expression and CRC occurrence was investigated in tumor and other tissues. Factors contributing to prognosis were evaluated using Kaplan-Meier survival analysis and Cox regression model. Results: p-FAK is apparently overexpressed in CRC and metastasis tissues. Compared with low p-FAK expression, patients with high p-FAK expression had shorter overall survival [hazard ratio (HR), 2.200; 95% confidence interval (CI), 1.265–3.452; p < 0.01] and disease-free survival (HR, 2.004; 95% CI 1.262–3.382; p < 0.01) in multivariate Cox analysis after adjusting other prognostic factors. High p-FAK expression was also related to a worse chemotherapeutic response in patients who achieved adjuvant chemotherapy (p < 0.01). Conclusion: Expression level of p-FAK is an independent risk factor and can serve as a prognostic biomarker for CRC. High p-FAK expression predicts an unfavorable prognosis of CRC as well as poor chemotherapeutic response. Frontiers Media S.A. 2022-09-13 /pmc/articles/PMC9513477/ /pubmed/36176444 http://dx.doi.org/10.3389/fphar.2022.989999 Text en Copyright © 2022 Yu, Xu, Zhou, Zheng, Zhu, Sui, Xin, Chang, Zhang and Cao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Yu, Guanyu
Xu, Mengnan
Zhou, Leqi
Zheng, Kuo
Zhu, Xiaoming
Sui, Jinke
Xin, Cheng
Chang, Wenjun
Zhang, Wei
Cao, Fuao
High expression of phosphorylated focal adhesion kinase predicts a poor prognosis in human colorectal cancer
title High expression of phosphorylated focal adhesion kinase predicts a poor prognosis in human colorectal cancer
title_full High expression of phosphorylated focal adhesion kinase predicts a poor prognosis in human colorectal cancer
title_fullStr High expression of phosphorylated focal adhesion kinase predicts a poor prognosis in human colorectal cancer
title_full_unstemmed High expression of phosphorylated focal adhesion kinase predicts a poor prognosis in human colorectal cancer
title_short High expression of phosphorylated focal adhesion kinase predicts a poor prognosis in human colorectal cancer
title_sort high expression of phosphorylated focal adhesion kinase predicts a poor prognosis in human colorectal cancer
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9513477/
https://www.ncbi.nlm.nih.gov/pubmed/36176444
http://dx.doi.org/10.3389/fphar.2022.989999
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