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Tenascin-C serum levels and its prognostic power in non-small cell lung cancer

BACKGROUND: Tenascin-C is overexpressed in the stroma of most solid malignancies and may function as a diagnostic tumor marker. This study was conducted to evaluate the potential significance of Tenascin-C as a predictive marker for tumor progression in the sera of non-small cell lung cancer (NSCLC)...

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Autores principales: Gebauer, Florian, Gelis, Suyin, Zander, Hilke, Meyer, Karl-Frederick, Wolters-Eisfeld, Gerrit, Izbicki, Jakob R., Bockhorn, Maximilian, Tachezy, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4991503/
https://www.ncbi.nlm.nih.gov/pubmed/26967391
http://dx.doi.org/10.18632/oncotarget.7976
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author Gebauer, Florian
Gelis, Suyin
Zander, Hilke
Meyer, Karl-Frederick
Wolters-Eisfeld, Gerrit
Izbicki, Jakob R.
Bockhorn, Maximilian
Tachezy, Michael
author_facet Gebauer, Florian
Gelis, Suyin
Zander, Hilke
Meyer, Karl-Frederick
Wolters-Eisfeld, Gerrit
Izbicki, Jakob R.
Bockhorn, Maximilian
Tachezy, Michael
author_sort Gebauer, Florian
collection PubMed
description BACKGROUND: Tenascin-C is overexpressed in the stroma of most solid malignancies and may function as a diagnostic tumor marker. This study was conducted to evaluate the potential significance of Tenascin-C as a predictive marker for tumor progression in the sera of non-small cell lung cancer (NSCLC) patients. RESULTS: Serum concentration of Tenascin-C is significantly elevated in NSCLC patients compared to healthy controls (p=0.013). The sensitivity of Tenascin-C in detecting NSCLC was 74% at a specificity of 57%. Elevated Tenascin-C serum values are associated with larger tumor size and lymph node involvement (p=0.022 and p=0.036, respectively). The Kaplan-Meyer-curves showed a significant association of Tenascin-C with the patient's overall survival (p=0.004), but not with the recurrence-free survival (p=0.328). METHODS: We quantified Tenascin-C in the sera of 103 NSCLC patients and 76 healthy blood donors by enzyme-linked immune-absorbance assay tests. Prognostic significance was determined by area under the curve analysis and Youden-index. The results were correlated with clinical, histopathological, and patient survival data (Chi-square test, Kaplan-Meier analysis, log-rank test, multivariate Cox-regression analysis). CONCLUSION: Although significantly elevated in patients with NSCLC, the sensitivity and specificity of the Tenascin-C serum quantification test was low. However, although failing to be an independent prognosticator in multivariate analysis, the results implicate Tenascin-C as a predictive prognostic marker for NSCLC patients. The data must be further validated in future prospective trials with larger patient cohorts.
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spelling pubmed-49915032016-09-01 Tenascin-C serum levels and its prognostic power in non-small cell lung cancer Gebauer, Florian Gelis, Suyin Zander, Hilke Meyer, Karl-Frederick Wolters-Eisfeld, Gerrit Izbicki, Jakob R. Bockhorn, Maximilian Tachezy, Michael Oncotarget Research Paper BACKGROUND: Tenascin-C is overexpressed in the stroma of most solid malignancies and may function as a diagnostic tumor marker. This study was conducted to evaluate the potential significance of Tenascin-C as a predictive marker for tumor progression in the sera of non-small cell lung cancer (NSCLC) patients. RESULTS: Serum concentration of Tenascin-C is significantly elevated in NSCLC patients compared to healthy controls (p=0.013). The sensitivity of Tenascin-C in detecting NSCLC was 74% at a specificity of 57%. Elevated Tenascin-C serum values are associated with larger tumor size and lymph node involvement (p=0.022 and p=0.036, respectively). The Kaplan-Meyer-curves showed a significant association of Tenascin-C with the patient's overall survival (p=0.004), but not with the recurrence-free survival (p=0.328). METHODS: We quantified Tenascin-C in the sera of 103 NSCLC patients and 76 healthy blood donors by enzyme-linked immune-absorbance assay tests. Prognostic significance was determined by area under the curve analysis and Youden-index. The results were correlated with clinical, histopathological, and patient survival data (Chi-square test, Kaplan-Meier analysis, log-rank test, multivariate Cox-regression analysis). CONCLUSION: Although significantly elevated in patients with NSCLC, the sensitivity and specificity of the Tenascin-C serum quantification test was low. However, although failing to be an independent prognosticator in multivariate analysis, the results implicate Tenascin-C as a predictive prognostic marker for NSCLC patients. The data must be further validated in future prospective trials with larger patient cohorts. Impact Journals LLC 2016-03-08 /pmc/articles/PMC4991503/ /pubmed/26967391 http://dx.doi.org/10.18632/oncotarget.7976 Text en Copyright: © 2016 Gebauer et al. http://creativecommons.org/licenses/by/2.5/ 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
Gebauer, Florian
Gelis, Suyin
Zander, Hilke
Meyer, Karl-Frederick
Wolters-Eisfeld, Gerrit
Izbicki, Jakob R.
Bockhorn, Maximilian
Tachezy, Michael
Tenascin-C serum levels and its prognostic power in non-small cell lung cancer
title Tenascin-C serum levels and its prognostic power in non-small cell lung cancer
title_full Tenascin-C serum levels and its prognostic power in non-small cell lung cancer
title_fullStr Tenascin-C serum levels and its prognostic power in non-small cell lung cancer
title_full_unstemmed Tenascin-C serum levels and its prognostic power in non-small cell lung cancer
title_short Tenascin-C serum levels and its prognostic power in non-small cell lung cancer
title_sort tenascin-c serum levels and its prognostic power in non-small cell lung cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4991503/
https://www.ncbi.nlm.nih.gov/pubmed/26967391
http://dx.doi.org/10.18632/oncotarget.7976
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