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Serum carboxypeptidaseA4 levels predict liver metastasis in colorectal carcinoma

Hepatic metastasis is the most critical prognostic factor for colorectal cancer (CRC), and early detection of CRC liver metastasis can significantly improve cancer patient outcomes. In this study, we examined the levels of CPA4 in CRC samples, and assessed the potential of serum CPA4 as a biomarker...

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Autores principales: Sun, Lichao, Guo, Chunguang, Burnett, Joseph, Yang, Zhihua, Ran, Yuliang, Sun, Duxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346670/
https://www.ncbi.nlm.nih.gov/pubmed/27780921
http://dx.doi.org/10.18632/oncotarget.12798
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author Sun, Lichao
Guo, Chunguang
Burnett, Joseph
Yang, Zhihua
Ran, Yuliang
Sun, Duxin
author_facet Sun, Lichao
Guo, Chunguang
Burnett, Joseph
Yang, Zhihua
Ran, Yuliang
Sun, Duxin
author_sort Sun, Lichao
collection PubMed
description Hepatic metastasis is the most critical prognostic factor for colorectal cancer (CRC), and early detection of CRC liver metastasis can significantly improve cancer patient outcomes. In this study, we examined the levels of CPA4 in CRC samples, and assessed the potential of serum CPA4 as a biomarker for predicting CRC liver metastasis. CPA4 positivity was observed in 68.4% (130/190) colorectal cancer tissues, and significantly correlated with Depth of invasion, Lymph node metastasis, Distant metastasis and Stage. In addition, high CPA4 expression was associated with poor overall survival, and was an independent prognostic marker in patients with CRC. In CRC serum samples, serum CPA4 concentrations in CRC-M1(S) patients (3717.89 ± 375.98 pg/mL) were significantly increased as compared to in CRC-M1(H) patients (3692.12 ± 261.51 pg/mL), CRC patients without liver metastasis (2480.47 ± 507.90 pg/mL) or healthy controls (2183.7 ± 621.7 pg/mL) (P < 0.05). Furthermore, high CPA4 concentration was significantly correlated with Distant metastasis, Lymph node involvement, Stage and poor overall survival of the patients with CRC. Logistic regression analysis revealed that serum CPA4 level and Lymph node metastasis were the significant parameters for predicting CRC liver metastasis. In leave-one-out-cross-validation, these two markers resulted in sensitivity (90.0%) and specificity (93.8%) for hepatic metastasis detection. Moreover, this combination could correctly classify 49 cases of the 50 CRC patients with heterochronous liver metastasis in an independent test set. Therefore, our results suggest that CPA4 is closely associated with CRC liver metastasis, and serum CPA4 concentration combined with lymph node involvement may be used as accurate predictors of liver metastasis in colorectal cancer.
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spelling pubmed-53466702017-03-30 Serum carboxypeptidaseA4 levels predict liver metastasis in colorectal carcinoma Sun, Lichao Guo, Chunguang Burnett, Joseph Yang, Zhihua Ran, Yuliang Sun, Duxin Oncotarget Research Paper Hepatic metastasis is the most critical prognostic factor for colorectal cancer (CRC), and early detection of CRC liver metastasis can significantly improve cancer patient outcomes. In this study, we examined the levels of CPA4 in CRC samples, and assessed the potential of serum CPA4 as a biomarker for predicting CRC liver metastasis. CPA4 positivity was observed in 68.4% (130/190) colorectal cancer tissues, and significantly correlated with Depth of invasion, Lymph node metastasis, Distant metastasis and Stage. In addition, high CPA4 expression was associated with poor overall survival, and was an independent prognostic marker in patients with CRC. In CRC serum samples, serum CPA4 concentrations in CRC-M1(S) patients (3717.89 ± 375.98 pg/mL) were significantly increased as compared to in CRC-M1(H) patients (3692.12 ± 261.51 pg/mL), CRC patients without liver metastasis (2480.47 ± 507.90 pg/mL) or healthy controls (2183.7 ± 621.7 pg/mL) (P < 0.05). Furthermore, high CPA4 concentration was significantly correlated with Distant metastasis, Lymph node involvement, Stage and poor overall survival of the patients with CRC. Logistic regression analysis revealed that serum CPA4 level and Lymph node metastasis were the significant parameters for predicting CRC liver metastasis. In leave-one-out-cross-validation, these two markers resulted in sensitivity (90.0%) and specificity (93.8%) for hepatic metastasis detection. Moreover, this combination could correctly classify 49 cases of the 50 CRC patients with heterochronous liver metastasis in an independent test set. Therefore, our results suggest that CPA4 is closely associated with CRC liver metastasis, and serum CPA4 concentration combined with lymph node involvement may be used as accurate predictors of liver metastasis in colorectal cancer. Impact Journals LLC 2016-10-21 /pmc/articles/PMC5346670/ /pubmed/27780921 http://dx.doi.org/10.18632/oncotarget.12798 Text en Copyright: © 2016 Sun et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Sun, Lichao
Guo, Chunguang
Burnett, Joseph
Yang, Zhihua
Ran, Yuliang
Sun, Duxin
Serum carboxypeptidaseA4 levels predict liver metastasis in colorectal carcinoma
title Serum carboxypeptidaseA4 levels predict liver metastasis in colorectal carcinoma
title_full Serum carboxypeptidaseA4 levels predict liver metastasis in colorectal carcinoma
title_fullStr Serum carboxypeptidaseA4 levels predict liver metastasis in colorectal carcinoma
title_full_unstemmed Serum carboxypeptidaseA4 levels predict liver metastasis in colorectal carcinoma
title_short Serum carboxypeptidaseA4 levels predict liver metastasis in colorectal carcinoma
title_sort serum carboxypeptidasea4 levels predict liver metastasis in colorectal carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346670/
https://www.ncbi.nlm.nih.gov/pubmed/27780921
http://dx.doi.org/10.18632/oncotarget.12798
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