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Serum Expression of β-Catenin Is a Potential Detection Marker in Patients with Colorectal Cancer

OBJECT: To investigate the correlation between the level of serum β-catenin and the disease progression of colorectal polyp (CRP) and colorectal cancer (CRC) and find its potential diagnostic value. METHODS: A total of 327 clinical serum samples and their electronic medical records were collected. D...

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Autores principales: Li, Shue, Huang, Mao, Liu, Qiao, Wang, Ding, Wu, Rui, Zhang, Xiuyu, Chen, Weixian, Duan, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6855041/
https://www.ncbi.nlm.nih.gov/pubmed/31781302
http://dx.doi.org/10.1155/2019/5070524
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author Li, Shue
Huang, Mao
Liu, Qiao
Wang, Ding
Wu, Rui
Zhang, Xiuyu
Chen, Weixian
Duan, Liang
author_facet Li, Shue
Huang, Mao
Liu, Qiao
Wang, Ding
Wu, Rui
Zhang, Xiuyu
Chen, Weixian
Duan, Liang
author_sort Li, Shue
collection PubMed
description OBJECT: To investigate the correlation between the level of serum β-catenin and the disease progression of colorectal polyp (CRP) and colorectal cancer (CRC) and find its potential diagnostic value. METHODS: A total of 327 clinical serum samples and their electronic medical records were collected. Detecting by enzyme-linked immunosorbent assay (ELISA), the correlations of serum β-catenin with tumor marker carcinoembryonic antigen (CEA) and CRC clinicopathological parameters and the receiver operating characteristic (ROC) curve were analyzed. RESULTS: Serum β-catenin levels in the CRP and CRC patients were significantly higher than those in the healthy control (HC) group (P < 0.05 and P < 0.001). Compared with CRP, serum β-catenin level in CRC was also increased (P < 0.05). However, there was no significant difference in gender, age, location, tumor size, Dukes staging, or metastasis (P > 0.05) between serum β-catenin and clinical parameters of CRC. There was no correlation between serum β-catenin levels and CEA in CRC patients (P = 0.14). ROC curve analysis showed that serum β-catenin possessed the maximum diagnostic efficiency in CRP (AUC = 0.73, P < 0.05) with 86.41% sensitivity and 51.56% specificity. β-Catenin combined with CEA had the highest diagnostic efficiency (AUC = 0.88, P < 0.05) with 81.88% sensitivity and 73.44% specificity. With CRC patients from CRP patients, ROC analysis of the combining detection (AUC = 0.70, P < 0.05) had the 70% sensitivity and 84.5% specificity. CONCLUSION: The serum β-catenin levels are gradually increased in CRP and CRC, while there is no correlation between its levels and CRC disease process. Single serum β-catenin or combined CEA would be one of the potential candidate biomarkers for colorectal disease diagnosis.
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spelling pubmed-68550412019-11-28 Serum Expression of β-Catenin Is a Potential Detection Marker in Patients with Colorectal Cancer Li, Shue Huang, Mao Liu, Qiao Wang, Ding Wu, Rui Zhang, Xiuyu Chen, Weixian Duan, Liang Dis Markers Research Article OBJECT: To investigate the correlation between the level of serum β-catenin and the disease progression of colorectal polyp (CRP) and colorectal cancer (CRC) and find its potential diagnostic value. METHODS: A total of 327 clinical serum samples and their electronic medical records were collected. Detecting by enzyme-linked immunosorbent assay (ELISA), the correlations of serum β-catenin with tumor marker carcinoembryonic antigen (CEA) and CRC clinicopathological parameters and the receiver operating characteristic (ROC) curve were analyzed. RESULTS: Serum β-catenin levels in the CRP and CRC patients were significantly higher than those in the healthy control (HC) group (P < 0.05 and P < 0.001). Compared with CRP, serum β-catenin level in CRC was also increased (P < 0.05). However, there was no significant difference in gender, age, location, tumor size, Dukes staging, or metastasis (P > 0.05) between serum β-catenin and clinical parameters of CRC. There was no correlation between serum β-catenin levels and CEA in CRC patients (P = 0.14). ROC curve analysis showed that serum β-catenin possessed the maximum diagnostic efficiency in CRP (AUC = 0.73, P < 0.05) with 86.41% sensitivity and 51.56% specificity. β-Catenin combined with CEA had the highest diagnostic efficiency (AUC = 0.88, P < 0.05) with 81.88% sensitivity and 73.44% specificity. With CRC patients from CRP patients, ROC analysis of the combining detection (AUC = 0.70, P < 0.05) had the 70% sensitivity and 84.5% specificity. CONCLUSION: The serum β-catenin levels are gradually increased in CRP and CRC, while there is no correlation between its levels and CRC disease process. Single serum β-catenin or combined CEA would be one of the potential candidate biomarkers for colorectal disease diagnosis. Hindawi 2019-10-24 /pmc/articles/PMC6855041/ /pubmed/31781302 http://dx.doi.org/10.1155/2019/5070524 Text en Copyright © 2019 Shue Li et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Li, Shue
Huang, Mao
Liu, Qiao
Wang, Ding
Wu, Rui
Zhang, Xiuyu
Chen, Weixian
Duan, Liang
Serum Expression of β-Catenin Is a Potential Detection Marker in Patients with Colorectal Cancer
title Serum Expression of β-Catenin Is a Potential Detection Marker in Patients with Colorectal Cancer
title_full Serum Expression of β-Catenin Is a Potential Detection Marker in Patients with Colorectal Cancer
title_fullStr Serum Expression of β-Catenin Is a Potential Detection Marker in Patients with Colorectal Cancer
title_full_unstemmed Serum Expression of β-Catenin Is a Potential Detection Marker in Patients with Colorectal Cancer
title_short Serum Expression of β-Catenin Is a Potential Detection Marker in Patients with Colorectal Cancer
title_sort serum expression of β-catenin is a potential detection marker in patients with colorectal cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6855041/
https://www.ncbi.nlm.nih.gov/pubmed/31781302
http://dx.doi.org/10.1155/2019/5070524
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