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Low claudin-6 expression correlates with poor prognosis in patients with non-small cell lung cancer
OBJECTIVE: Claudins are found in junctional complexes mediating cell adhesion and are involved in the attachment of tight junctions to the underlying cytoskeleton. Abnormal claudin-6 expression has been observed for a variety of malignant solid tumors, but the expression of claudin-6 in non-small ce...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4527519/ https://www.ncbi.nlm.nih.gov/pubmed/26261421 http://dx.doi.org/10.2147/OTT.S85478 |
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author | Wang, Qiang Zhang, Yan Zhang, Tao Han, Zhi-Gang Shan, Li |
author_facet | Wang, Qiang Zhang, Yan Zhang, Tao Han, Zhi-Gang Shan, Li |
author_sort | Wang, Qiang |
collection | PubMed |
description | OBJECTIVE: Claudins are found in junctional complexes mediating cell adhesion and are involved in the attachment of tight junctions to the underlying cytoskeleton. Abnormal claudin-6 expression has been observed for a variety of malignant solid tumors, but the expression of claudin-6 in non-small cell lung cancer (NSCLC) has not yet been characterized. METHODS: Immunohistochemistry, reverse transcription-polymerase chain reaction (RT-PCR), and western blot analysis were used to quantify claudin-6 expression in 123 cases of NSCLC and non-cancerous adjacent tissue. We analyzed the relationship between claudin-6 expression and clinicopathological features of NSCLC. The Kaplan–Meier method was used to analyze postoperative survival rates, and the log-rank test was used to assess differences in survival rates. The Cox regression model was used to perform multivariate analysis. RESULTS: Claudin-6 expression was low for 61 of 123 (49.6%) NSCLC tissue samples and for 33 of 123 (26.8%) normal adjacent tissue samples. RT-PCR and western blot analyses confirmed the immunohistochemistry results. Claudin-6 expression was associated with lymph node metastasis (P<0.001) and TNM stage (P=0.007). Kaplan–Meier analysis indicated that patients with low claudin-6 expression had significantly lower survival rates than those with high claudin-6 expression. Multivariate analysis suggested that low claudin-6 expression was an independent indicator of prognosis in NSCLC patients. CONCLUSION: Low claudin-6 expression is an independent prognostic biomarker that indicates a worse prognosis in patients with NSCLC. |
format | Online Article Text |
id | pubmed-4527519 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-45275192015-08-10 Low claudin-6 expression correlates with poor prognosis in patients with non-small cell lung cancer Wang, Qiang Zhang, Yan Zhang, Tao Han, Zhi-Gang Shan, Li Onco Targets Ther Original Research OBJECTIVE: Claudins are found in junctional complexes mediating cell adhesion and are involved in the attachment of tight junctions to the underlying cytoskeleton. Abnormal claudin-6 expression has been observed for a variety of malignant solid tumors, but the expression of claudin-6 in non-small cell lung cancer (NSCLC) has not yet been characterized. METHODS: Immunohistochemistry, reverse transcription-polymerase chain reaction (RT-PCR), and western blot analysis were used to quantify claudin-6 expression in 123 cases of NSCLC and non-cancerous adjacent tissue. We analyzed the relationship between claudin-6 expression and clinicopathological features of NSCLC. The Kaplan–Meier method was used to analyze postoperative survival rates, and the log-rank test was used to assess differences in survival rates. The Cox regression model was used to perform multivariate analysis. RESULTS: Claudin-6 expression was low for 61 of 123 (49.6%) NSCLC tissue samples and for 33 of 123 (26.8%) normal adjacent tissue samples. RT-PCR and western blot analyses confirmed the immunohistochemistry results. Claudin-6 expression was associated with lymph node metastasis (P<0.001) and TNM stage (P=0.007). Kaplan–Meier analysis indicated that patients with low claudin-6 expression had significantly lower survival rates than those with high claudin-6 expression. Multivariate analysis suggested that low claudin-6 expression was an independent indicator of prognosis in NSCLC patients. CONCLUSION: Low claudin-6 expression is an independent prognostic biomarker that indicates a worse prognosis in patients with NSCLC. Dove Medical Press 2015-07-31 /pmc/articles/PMC4527519/ /pubmed/26261421 http://dx.doi.org/10.2147/OTT.S85478 Text en © 2015 Wang et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Wang, Qiang Zhang, Yan Zhang, Tao Han, Zhi-Gang Shan, Li Low claudin-6 expression correlates with poor prognosis in patients with non-small cell lung cancer |
title | Low claudin-6 expression correlates with poor prognosis in patients with non-small cell lung cancer |
title_full | Low claudin-6 expression correlates with poor prognosis in patients with non-small cell lung cancer |
title_fullStr | Low claudin-6 expression correlates with poor prognosis in patients with non-small cell lung cancer |
title_full_unstemmed | Low claudin-6 expression correlates with poor prognosis in patients with non-small cell lung cancer |
title_short | Low claudin-6 expression correlates with poor prognosis in patients with non-small cell lung cancer |
title_sort | low claudin-6 expression correlates with poor prognosis in patients with non-small cell lung cancer |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4527519/ https://www.ncbi.nlm.nih.gov/pubmed/26261421 http://dx.doi.org/10.2147/OTT.S85478 |
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