Published June 4, 2014 | Version v1
Journal article

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

  • 1. Department of thoracic surgery, Tangdu hospital, Fourth Military Medical University, Xi'an (China)

Description

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. 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. 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). Our results indicate that NOK expression is of clinical significance and can serve as a prognostic biomarker in NSCLC

Availability note (English)

Available from http://dx.doi.org/10.1186/1471-2407-14-402; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051150

Additional details

Publishing Information

Journal Title
BMC cancer (Online)
Journal Volume
14
Journal Page Range
p. 402
ISSN
1471-2407

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
47000971
Subject category
S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
HAZARDS; LUNGS; MULTIVARIATE ANALYSIS; ONCOGENES; PATIENTS; PROTEINS; SURVIVAL TIME; TUMOR CELLS
Descriptors DEC
ANIMAL CELLS; BODY; GENES; MATHEMATICS; ORGANIC COMPOUNDS; ORGANS; RESPIRATORY SYSTEM; STATISTICS

Optional Information

Copyright
Copyright (c) 2014 Chen et al.
Notes
PMCID: PMC4051150; PUBLISHER-ID: 1471-2407-14-402; PMID: 24894011; OAI: oai:pubmedcentral.nih.gov:4051150; licensee BioMed Central Ltd.