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PTK7 overexpression in colorectal tumors: Clinicopathological correlation and prognosis relevance

Colorectal cancer (CRC) has one of the highest mortality rates in the worldwide and its incidence has been increasing in recent years. Protein tyrosine kinase-7 (PTK7) is an inactive member of receptor protein tyrosine kinase (RPTK)-like molecules, which is involved in tumorigenesis of a variety of...

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Autores principales: Tian, Xiuyun, Yan, Liang, Zhang, Donghai, Guan, Xiaoya, Dong, Bin, Zhao, Min, Hao, Chunyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5022898/
https://www.ncbi.nlm.nih.gov/pubmed/27499181
http://dx.doi.org/10.3892/or.2016.4983
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author Tian, Xiuyun
Yan, Liang
Zhang, Donghai
Guan, Xiaoya
Dong, Bin
Zhao, Min
Hao, Chunyi
author_facet Tian, Xiuyun
Yan, Liang
Zhang, Donghai
Guan, Xiaoya
Dong, Bin
Zhao, Min
Hao, Chunyi
author_sort Tian, Xiuyun
collection PubMed
description Colorectal cancer (CRC) has one of the highest mortality rates in the worldwide and its incidence has been increasing in recent years. Protein tyrosine kinase-7 (PTK7) is an inactive member of receptor protein tyrosine kinase (RPTK)-like molecules, which is involved in tumorigenesis of a variety of cancers. Our study aimed to investigate expression of PTK7 in colorectal tumors (including benign adenomas and malignant carcinomas), and its potential function in tumorigenesis and prognosis. A total of 209 CRC patients and 28 colonic adenoma patients were included in this study. Reverse transcription polymerase chain reaction (RT-PCR) and quantitative real-time PCR were performed in 14 pairs of fresh frozen tissues to evaluate mRNA expression of PTK7. Expression of PTK7 protein in 209 CRC tissues with paired non-cancerous mucosa and 28 adenoma specimens were tested using immunohistochemistry. The expression difference and its correlation with clinicopathological features and overall survival were assessed by SPSS statistics (version 22). P<0.05 was considered significant. RT-PCR and quantitative real-time PCR showed a higher expression of PTK7 mRNA in CRC compared with non-tumorous mucosa (4.87±3.71 vs. 1.33±1.05; P<0.001). PTK7 expression was significantly higher in adenoma (75%) and CRC (68.3%) than in non-tumorous mucosa (P<0.001). PTK7 expression was correlated with tumor differentiation (P=0.027), lymph node metastasis (P=0.005), distant metastasis (P=0.001) and TNM stage (P=0.028) of CRC patients. Significant correlation between PTK7 overexpression and favorable overall survival of CRC patients was observed (P=0.005). Therefore, it may act as a candidate biomarker to predict the occurrence and prognosis of colorectal tumor.
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spelling pubmed-50228982016-09-22 PTK7 overexpression in colorectal tumors: Clinicopathological correlation and prognosis relevance Tian, Xiuyun Yan, Liang Zhang, Donghai Guan, Xiaoya Dong, Bin Zhao, Min Hao, Chunyi Oncol Rep Articles Colorectal cancer (CRC) has one of the highest mortality rates in the worldwide and its incidence has been increasing in recent years. Protein tyrosine kinase-7 (PTK7) is an inactive member of receptor protein tyrosine kinase (RPTK)-like molecules, which is involved in tumorigenesis of a variety of cancers. Our study aimed to investigate expression of PTK7 in colorectal tumors (including benign adenomas and malignant carcinomas), and its potential function in tumorigenesis and prognosis. A total of 209 CRC patients and 28 colonic adenoma patients were included in this study. Reverse transcription polymerase chain reaction (RT-PCR) and quantitative real-time PCR were performed in 14 pairs of fresh frozen tissues to evaluate mRNA expression of PTK7. Expression of PTK7 protein in 209 CRC tissues with paired non-cancerous mucosa and 28 adenoma specimens were tested using immunohistochemistry. The expression difference and its correlation with clinicopathological features and overall survival were assessed by SPSS statistics (version 22). P<0.05 was considered significant. RT-PCR and quantitative real-time PCR showed a higher expression of PTK7 mRNA in CRC compared with non-tumorous mucosa (4.87±3.71 vs. 1.33±1.05; P<0.001). PTK7 expression was significantly higher in adenoma (75%) and CRC (68.3%) than in non-tumorous mucosa (P<0.001). PTK7 expression was correlated with tumor differentiation (P=0.027), lymph node metastasis (P=0.005), distant metastasis (P=0.001) and TNM stage (P=0.028) of CRC patients. Significant correlation between PTK7 overexpression and favorable overall survival of CRC patients was observed (P=0.005). Therefore, it may act as a candidate biomarker to predict the occurrence and prognosis of colorectal tumor. D.A. Spandidos 2016-10 2016-07-28 /pmc/articles/PMC5022898/ /pubmed/27499181 http://dx.doi.org/10.3892/or.2016.4983 Text en Copyright: © Tian et al. 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
Tian, Xiuyun
Yan, Liang
Zhang, Donghai
Guan, Xiaoya
Dong, Bin
Zhao, Min
Hao, Chunyi
PTK7 overexpression in colorectal tumors: Clinicopathological correlation and prognosis relevance
title PTK7 overexpression in colorectal tumors: Clinicopathological correlation and prognosis relevance
title_full PTK7 overexpression in colorectal tumors: Clinicopathological correlation and prognosis relevance
title_fullStr PTK7 overexpression in colorectal tumors: Clinicopathological correlation and prognosis relevance
title_full_unstemmed PTK7 overexpression in colorectal tumors: Clinicopathological correlation and prognosis relevance
title_short PTK7 overexpression in colorectal tumors: Clinicopathological correlation and prognosis relevance
title_sort ptk7 overexpression in colorectal tumors: clinicopathological correlation and prognosis relevance
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5022898/
https://www.ncbi.nlm.nih.gov/pubmed/27499181
http://dx.doi.org/10.3892/or.2016.4983
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