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Overexpression of CHD1L is positively associated with metastasis of lung adenocarcinoma and predicts patients poor survival
CHD1L (chromodomain helicase/ATPase DNA binding protein 1-like gene) has been demonstrated as an oncogene in hepatocellular carcinoma (HCC), however, the role of CHD1L in non-small-cell lung cancer (NSCLC) tumorigenesis hasn't been elucidated. In this study, the expression and amplification sta...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4741596/ https://www.ncbi.nlm.nih.gov/pubmed/26360781 |
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author | He, Li-Ru Ma, Ning-Fang Chen, Jie-Wei Li, Bin-Kui Guan, Xin-Yuan Liu, Meng-Zhong Xie, Dan |
author_facet | He, Li-Ru Ma, Ning-Fang Chen, Jie-Wei Li, Bin-Kui Guan, Xin-Yuan Liu, Meng-Zhong Xie, Dan |
author_sort | He, Li-Ru |
collection | PubMed |
description | CHD1L (chromodomain helicase/ATPase DNA binding protein 1-like gene) has been demonstrated as an oncogene in hepatocellular carcinoma (HCC), however, the role of CHD1L in non-small-cell lung cancer (NSCLC) tumorigenesis hasn't been elucidated. In this study, the expression and amplification status of CHD1L were examined by immunohistochemistry and fluorescence in situ hybridization respectively in 248 surgically resected NSCLCs. The associations between CHD1L expression and clinicopathologic features and the prognostic value of CHD1L were analyzed. Overexpression and amplification of CHD1L was found in 42.1% and 17.7% of NSCLCs, respectively. The frequency of CHD1L overexpression (53.2% vs. 28.1%, P = 0.002) and amplification (25.2% vs. 8.2%, P = 0.020) in adenocarcinoma (ADC), was much higher than that in squamous cell carcinoma (SCC). CHD1L overexpression was associated closely with ascending pN status (P < 0.001), advanced clinical stage (P = 0.001) and tumor distant metastasis (P = 0.001) in ADCs, but not in SCCs. For the whole cohort and ADC patients, univariate survival analysis demonstrated a significant association of CHD1L overexpression with shortened survival; and in multivariate analysis, CHD1L overexpression was evaluated as a independent predictor for overall survival and distant metastasis free survival. These results suggested that overexpression of CHD1L is positively associated with tumor metastasis of lung ADC, and might serve as a novel prognostic biomarker and potential therapeutic target for lung ADC patients. |
format | Online Article Text |
id | pubmed-4741596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-47415962016-03-03 Overexpression of CHD1L is positively associated with metastasis of lung adenocarcinoma and predicts patients poor survival He, Li-Ru Ma, Ning-Fang Chen, Jie-Wei Li, Bin-Kui Guan, Xin-Yuan Liu, Meng-Zhong Xie, Dan Oncotarget Research Paper CHD1L (chromodomain helicase/ATPase DNA binding protein 1-like gene) has been demonstrated as an oncogene in hepatocellular carcinoma (HCC), however, the role of CHD1L in non-small-cell lung cancer (NSCLC) tumorigenesis hasn't been elucidated. In this study, the expression and amplification status of CHD1L were examined by immunohistochemistry and fluorescence in situ hybridization respectively in 248 surgically resected NSCLCs. The associations between CHD1L expression and clinicopathologic features and the prognostic value of CHD1L were analyzed. Overexpression and amplification of CHD1L was found in 42.1% and 17.7% of NSCLCs, respectively. The frequency of CHD1L overexpression (53.2% vs. 28.1%, P = 0.002) and amplification (25.2% vs. 8.2%, P = 0.020) in adenocarcinoma (ADC), was much higher than that in squamous cell carcinoma (SCC). CHD1L overexpression was associated closely with ascending pN status (P < 0.001), advanced clinical stage (P = 0.001) and tumor distant metastasis (P = 0.001) in ADCs, but not in SCCs. For the whole cohort and ADC patients, univariate survival analysis demonstrated a significant association of CHD1L overexpression with shortened survival; and in multivariate analysis, CHD1L overexpression was evaluated as a independent predictor for overall survival and distant metastasis free survival. These results suggested that overexpression of CHD1L is positively associated with tumor metastasis of lung ADC, and might serve as a novel prognostic biomarker and potential therapeutic target for lung ADC patients. Impact Journals LLC 2015-08-24 /pmc/articles/PMC4741596/ /pubmed/26360781 Text en Copyright: © 2015 He 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 He, Li-Ru Ma, Ning-Fang Chen, Jie-Wei Li, Bin-Kui Guan, Xin-Yuan Liu, Meng-Zhong Xie, Dan Overexpression of CHD1L is positively associated with metastasis of lung adenocarcinoma and predicts patients poor survival |
title | Overexpression of CHD1L is positively associated with metastasis of lung adenocarcinoma and predicts patients poor survival |
title_full | Overexpression of CHD1L is positively associated with metastasis of lung adenocarcinoma and predicts patients poor survival |
title_fullStr | Overexpression of CHD1L is positively associated with metastasis of lung adenocarcinoma and predicts patients poor survival |
title_full_unstemmed | Overexpression of CHD1L is positively associated with metastasis of lung adenocarcinoma and predicts patients poor survival |
title_short | Overexpression of CHD1L is positively associated with metastasis of lung adenocarcinoma and predicts patients poor survival |
title_sort | overexpression of chd1l is positively associated with metastasis of lung adenocarcinoma and predicts patients poor survival |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4741596/ https://www.ncbi.nlm.nih.gov/pubmed/26360781 |
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