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Prognostic value of molecular events from negative surgical margin of non-small-cell lung cancer
It is hypothesized that the molecular status in negative surgical margin (NSM) is associated with prognosis of cancer patients. In this study, the prognostic relevance of Epithelial-to-Mesenchymal Transition (EMT) molecular events in NSMs in patients with NSCLC was investigated. EMT model was develo...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5581137/ https://www.ncbi.nlm.nih.gov/pubmed/28881838 http://dx.doi.org/10.18632/oncotarget.10949 |
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author | Cao, Bangrong Feng, Lin Lu, Dan Liu, Yan Liu, Yu Guo, Suping Han, Naijun Liu, Xiangyang Mao, Yousheng He, Jie Cheng, Shujun Gao, Yanning Zhang, Kaitai |
author_facet | Cao, Bangrong Feng, Lin Lu, Dan Liu, Yan Liu, Yu Guo, Suping Han, Naijun Liu, Xiangyang Mao, Yousheng He, Jie Cheng, Shujun Gao, Yanning Zhang, Kaitai |
author_sort | Cao, Bangrong |
collection | PubMed |
description | It is hypothesized that the molecular status in negative surgical margin (NSM) is associated with prognosis of cancer patients. In this study, the prognostic relevance of Epithelial-to-Mesenchymal Transition (EMT) molecular events in NSMs in patients with NSCLC was investigated. EMT model was developed, in which the mesenchymal transition of human immortalized bronchial epithelial cell line was induced by TGF-beta1. Gene expression of EMT-induced cells and NSMs from 60 lung squamous cell carcinoma (SCC) patients was profiled by microarray and validated by quantitative RT-PCR. Two independent cohorts (lung SCC, n = 50; NSCLC, n = 54) were employed to validate the prognostic value of candidate genes. A set of 1490 genes were identified in EMT model in vitro. An EMT-like gene-expression pattern by 33 essential genes was optimized in NSMs, and was significantly associated with tumor progression. The 33 genes also exhibited a site-dependent field cancerization effect in the normal-appearing airways adjacent to NSCLCs. In the independent lung SCC cohort, the EMT-like active pattern indicated poor outcome of patients (n = 50, log-rank p = 0.009). Furthermore, in the NSCLC cohort, patients with EMT-like active pattern had shorter predictive survival time (n = 54, log-rank p = 0.02). In conclusion, the existence of EMT-like gene expression in NSMs, may play critical role in tumor progression and be a potential biomarker for prognosis in patients with NSCLC. |
format | Online Article Text |
id | pubmed-5581137 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-55811372017-09-06 Prognostic value of molecular events from negative surgical margin of non-small-cell lung cancer Cao, Bangrong Feng, Lin Lu, Dan Liu, Yan Liu, Yu Guo, Suping Han, Naijun Liu, Xiangyang Mao, Yousheng He, Jie Cheng, Shujun Gao, Yanning Zhang, Kaitai Oncotarget Clinical Research Paper It is hypothesized that the molecular status in negative surgical margin (NSM) is associated with prognosis of cancer patients. In this study, the prognostic relevance of Epithelial-to-Mesenchymal Transition (EMT) molecular events in NSMs in patients with NSCLC was investigated. EMT model was developed, in which the mesenchymal transition of human immortalized bronchial epithelial cell line was induced by TGF-beta1. Gene expression of EMT-induced cells and NSMs from 60 lung squamous cell carcinoma (SCC) patients was profiled by microarray and validated by quantitative RT-PCR. Two independent cohorts (lung SCC, n = 50; NSCLC, n = 54) were employed to validate the prognostic value of candidate genes. A set of 1490 genes were identified in EMT model in vitro. An EMT-like gene-expression pattern by 33 essential genes was optimized in NSMs, and was significantly associated with tumor progression. The 33 genes also exhibited a site-dependent field cancerization effect in the normal-appearing airways adjacent to NSCLCs. In the independent lung SCC cohort, the EMT-like active pattern indicated poor outcome of patients (n = 50, log-rank p = 0.009). Furthermore, in the NSCLC cohort, patients with EMT-like active pattern had shorter predictive survival time (n = 54, log-rank p = 0.02). In conclusion, the existence of EMT-like gene expression in NSMs, may play critical role in tumor progression and be a potential biomarker for prognosis in patients with NSCLC. Impact Journals LLC 2016-07-29 /pmc/articles/PMC5581137/ /pubmed/28881838 http://dx.doi.org/10.18632/oncotarget.10949 Text en Copyright: © 2017 Cao et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Clinical Research Paper Cao, Bangrong Feng, Lin Lu, Dan Liu, Yan Liu, Yu Guo, Suping Han, Naijun Liu, Xiangyang Mao, Yousheng He, Jie Cheng, Shujun Gao, Yanning Zhang, Kaitai Prognostic value of molecular events from negative surgical margin of non-small-cell lung cancer |
title | Prognostic value of molecular events from negative surgical margin of non-small-cell lung cancer |
title_full | Prognostic value of molecular events from negative surgical margin of non-small-cell lung cancer |
title_fullStr | Prognostic value of molecular events from negative surgical margin of non-small-cell lung cancer |
title_full_unstemmed | Prognostic value of molecular events from negative surgical margin of non-small-cell lung cancer |
title_short | Prognostic value of molecular events from negative surgical margin of non-small-cell lung cancer |
title_sort | prognostic value of molecular events from negative surgical margin of non-small-cell lung cancer |
topic | Clinical Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5581137/ https://www.ncbi.nlm.nih.gov/pubmed/28881838 http://dx.doi.org/10.18632/oncotarget.10949 |
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