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Clinicopathologic features and prognostic implications of NOK/STYK1 protein expression in non-small cell lung cancer

BACKGROUND: The expression of novel oncogenic kinase (NOK), a member of the protein tyrosine kinase (PTK) family, has been observed in several human malignancies including non-small cell lung cancer (NSCLC). However, the clinic relevance of NOK expression in NSCLC remains unclear. METHODS: In this s...

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Autores principales: Chen, Peng, Li, Wei-Miao, Lu, Qiang, Wang, Jian, Yan, Xiao-Long, Zhang, Zhi-Pei, Li, Xiao-Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051150/
https://www.ncbi.nlm.nih.gov/pubmed/24894011
http://dx.doi.org/10.1186/1471-2407-14-402
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author Chen, Peng
Li, Wei-Miao
Lu, Qiang
Wang, Jian
Yan, Xiao-Long
Zhang, Zhi-Pei
Li, Xiao-Fei
author_facet Chen, Peng
Li, Wei-Miao
Lu, Qiang
Wang, Jian
Yan, Xiao-Long
Zhang, Zhi-Pei
Li, Xiao-Fei
author_sort Chen, Peng
collection PubMed
description BACKGROUND: The expression of novel oncogenic kinase (NOK), a member of the protein tyrosine kinase (PTK) family, has been observed in several human malignancies including non-small cell lung cancer (NSCLC). However, the clinic relevance of NOK expression in NSCLC remains unclear. METHODS: In this study, NOK expression in tumor cells was assessed using immunohistochemical methods in 191 patients with resected NSCLC. The association of NOK expression with clinicopathological parameters, including the Ki-67 labeling index (LI), was also evaluated. Kaplan-Meier survival analysis and Cox proportional hazards models were used to estimate the effect of NOK expression on survival. RESULTS: Data showed that NOK was expressed in 75.4% and 14.1% of cancer lesions and corresponding adjacent non-cancerous tissue, respectively. Out of all the clinicopathological factors analyzed, NOK expression was significantly correlated with the grade of tumor differentiation (P = 0.035), pTNM stage (P = 0.020), lymphatic metastasis (P = 0.005) and high Ki-67 LI (P < 0.001). NOK positive NSCLC patients had a significantly shorter survival time (P = 0.004, Log-rank test) and the prognostic significance of NOK expression was apparent in squamous cell carcinoma patients (P = 0.022). Multivariate analysis indicated that NOK expression may be an independent prognostic factor in NSCLC (hazard ratio [HR], 1.731; P = 0.043). CONCLUSIONS: Our results indicate that NOK expression is of clinical significance and can serve as a prognostic biomarker in NSCLC.
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spelling pubmed-40511502014-06-11 Clinicopathologic features and prognostic implications of NOK/STYK1 protein expression in non-small cell lung cancer Chen, Peng Li, Wei-Miao Lu, Qiang Wang, Jian Yan, Xiao-Long Zhang, Zhi-Pei Li, Xiao-Fei BMC Cancer Research Article BACKGROUND: The expression of novel oncogenic kinase (NOK), a member of the protein tyrosine kinase (PTK) family, has been observed in several human malignancies including non-small cell lung cancer (NSCLC). However, the clinic relevance of NOK expression in NSCLC remains unclear. METHODS: In this study, NOK expression in tumor cells was assessed using immunohistochemical methods in 191 patients with resected NSCLC. The association of NOK expression with clinicopathological parameters, including the Ki-67 labeling index (LI), was also evaluated. Kaplan-Meier survival analysis and Cox proportional hazards models were used to estimate the effect of NOK expression on survival. RESULTS: Data showed that NOK was expressed in 75.4% and 14.1% of cancer lesions and corresponding adjacent non-cancerous tissue, respectively. Out of all the clinicopathological factors analyzed, NOK expression was significantly correlated with the grade of tumor differentiation (P = 0.035), pTNM stage (P = 0.020), lymphatic metastasis (P = 0.005) and high Ki-67 LI (P < 0.001). NOK positive NSCLC patients had a significantly shorter survival time (P = 0.004, Log-rank test) and the prognostic significance of NOK expression was apparent in squamous cell carcinoma patients (P = 0.022). Multivariate analysis indicated that NOK expression may be an independent prognostic factor in NSCLC (hazard ratio [HR], 1.731; P = 0.043). CONCLUSIONS: Our results indicate that NOK expression is of clinical significance and can serve as a prognostic biomarker in NSCLC. BioMed Central 2014-06-04 /pmc/articles/PMC4051150/ /pubmed/24894011 http://dx.doi.org/10.1186/1471-2407-14-402 Text en Copyright © 2014 Chen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Chen, Peng
Li, Wei-Miao
Lu, Qiang
Wang, Jian
Yan, Xiao-Long
Zhang, Zhi-Pei
Li, Xiao-Fei
Clinicopathologic features and prognostic implications of NOK/STYK1 protein expression in non-small cell lung cancer
title Clinicopathologic features and prognostic implications of NOK/STYK1 protein expression in non-small cell lung cancer
title_full Clinicopathologic features and prognostic implications of NOK/STYK1 protein expression in non-small cell lung cancer
title_fullStr Clinicopathologic features and prognostic implications of NOK/STYK1 protein expression in non-small cell lung cancer
title_full_unstemmed Clinicopathologic features and prognostic implications of NOK/STYK1 protein expression in non-small cell lung cancer
title_short Clinicopathologic features and prognostic implications of NOK/STYK1 protein expression in non-small cell lung cancer
title_sort clinicopathologic features and prognostic implications of nok/styk1 protein expression in non-small cell lung cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051150/
https://www.ncbi.nlm.nih.gov/pubmed/24894011
http://dx.doi.org/10.1186/1471-2407-14-402
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