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Expression and prognostic relevance of MET and phospho-BAD in non-small cell lung cancer
BACKGROUND: MET is involved in the progression of several types of human cancers, while phospho-BAD(Ser-136) is a key molecule in apoptosis and might be regulated by MET. The aim of this study was to investigate the correlation between altered expression of MET and phospho-BAD in non-small cell lung...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3787924/ https://www.ncbi.nlm.nih.gov/pubmed/24092988 http://dx.doi.org/10.2147/OTT.S50428 |
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author | Sun, Wenze Ai, Ting Gao, Ying Zhang, Yingbing Cui, Jie Song, Liping |
author_facet | Sun, Wenze Ai, Ting Gao, Ying Zhang, Yingbing Cui, Jie Song, Liping |
author_sort | Sun, Wenze |
collection | PubMed |
description | BACKGROUND: MET is involved in the progression of several types of human cancers, while phospho-BAD(Ser-136) is a key molecule in apoptosis and might be regulated by MET. The aim of this study was to investigate the correlation between altered expression of MET and phospho-BAD in non-small cell lung cancer (NSCLC) and their association with clinicopathologic parameters and overall survival. METHODS: MET and phospho-BAD(Ser-136) proteins were evaluated by immunohistochemical analysis in 183 paraffin-embedded specimens and were also assessed by Western blotting analysis in 12 frozen tumor tissue samples, which were representative examples of immunohistochemical staining. RESULTS: Positive expression of MET and phospho-BAD(Ser-136) occurred in 67.2% and 49.2% of the 183 cases of NSCLC, respectively. However, neither MET expression nor phospho-BAD(Ser-136) expression was associated with any clinicopathologic parameter. A significant correlation was found between MET and phospho-BAD(Ser-136) expression levels evaluated by immunohistochemistry (r = 0.268, P < 0.001). Overexpression of MET was significantly associated with shortened overall survival in univariate analysis (P < 0.001). Moreover, patients with a MET+/phospho-BAD(Ser-136)+ phenotype had a poorer prognosis than others (P < 0.001). Multivariate Cox proportional hazard analysis confirmed that MET expression is a prognostic factor for NSCLC. CONCLUSION: MET expression might be correlated with phospho-BAD(Ser-136) expression, and may be an adverse predictor for NSCLC. Activation of the MET/phospho-BAD(Ser-136) signaling pathway might play a role in the development and progression of NSCLC. |
format | Online Article Text |
id | pubmed-3787924 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-37879242013-10-03 Expression and prognostic relevance of MET and phospho-BAD in non-small cell lung cancer Sun, Wenze Ai, Ting Gao, Ying Zhang, Yingbing Cui, Jie Song, Liping Onco Targets Ther Original Research BACKGROUND: MET is involved in the progression of several types of human cancers, while phospho-BAD(Ser-136) is a key molecule in apoptosis and might be regulated by MET. The aim of this study was to investigate the correlation between altered expression of MET and phospho-BAD in non-small cell lung cancer (NSCLC) and their association with clinicopathologic parameters and overall survival. METHODS: MET and phospho-BAD(Ser-136) proteins were evaluated by immunohistochemical analysis in 183 paraffin-embedded specimens and were also assessed by Western blotting analysis in 12 frozen tumor tissue samples, which were representative examples of immunohistochemical staining. RESULTS: Positive expression of MET and phospho-BAD(Ser-136) occurred in 67.2% and 49.2% of the 183 cases of NSCLC, respectively. However, neither MET expression nor phospho-BAD(Ser-136) expression was associated with any clinicopathologic parameter. A significant correlation was found between MET and phospho-BAD(Ser-136) expression levels evaluated by immunohistochemistry (r = 0.268, P < 0.001). Overexpression of MET was significantly associated with shortened overall survival in univariate analysis (P < 0.001). Moreover, patients with a MET+/phospho-BAD(Ser-136)+ phenotype had a poorer prognosis than others (P < 0.001). Multivariate Cox proportional hazard analysis confirmed that MET expression is a prognostic factor for NSCLC. CONCLUSION: MET expression might be correlated with phospho-BAD(Ser-136) expression, and may be an adverse predictor for NSCLC. Activation of the MET/phospho-BAD(Ser-136) signaling pathway might play a role in the development and progression of NSCLC. Dove Medical Press 2013-09-18 /pmc/articles/PMC3787924/ /pubmed/24092988 http://dx.doi.org/10.2147/OTT.S50428 Text en © 2013 Sun et al. This work is published by Dove Medical Press Ltd, 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 Ltd, provided the work is properly attributed. |
spellingShingle | Original Research Sun, Wenze Ai, Ting Gao, Ying Zhang, Yingbing Cui, Jie Song, Liping Expression and prognostic relevance of MET and phospho-BAD in non-small cell lung cancer |
title | Expression and prognostic relevance of MET and phospho-BAD in non-small cell lung cancer |
title_full | Expression and prognostic relevance of MET and phospho-BAD in non-small cell lung cancer |
title_fullStr | Expression and prognostic relevance of MET and phospho-BAD in non-small cell lung cancer |
title_full_unstemmed | Expression and prognostic relevance of MET and phospho-BAD in non-small cell lung cancer |
title_short | Expression and prognostic relevance of MET and phospho-BAD in non-small cell lung cancer |
title_sort | expression and prognostic relevance of met and phospho-bad in non-small cell lung cancer |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3787924/ https://www.ncbi.nlm.nih.gov/pubmed/24092988 http://dx.doi.org/10.2147/OTT.S50428 |
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