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Prognostic significance of stem cell-related marker expression and its correlation with histologic subtypes in lung adenocarcinoma
Cancer stem cells (CSCs) are a small subset of tumor cells that exhibit stem cell-like properties and contribute in treatment failure. To clarify the expression and prognostic significance of several CSC markers in non-small cell lung cancer, we retrospectively analyzed 368 patients with adenocarcin...
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/PMC5173151/ https://www.ncbi.nlm.nih.gov/pubmed/27285762 http://dx.doi.org/10.18632/oncotarget.9894 |
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author | Park, Eunhyang Park, Soo Young Sun, Ping-Li Jin, Yan Kim, Ji Eun Jheon, Sanghoon Kim, Kwhanmien Lee, Choon Taek Kim, Hyojin Chung, Jin-Haeng |
author_facet | Park, Eunhyang Park, Soo Young Sun, Ping-Li Jin, Yan Kim, Ji Eun Jheon, Sanghoon Kim, Kwhanmien Lee, Choon Taek Kim, Hyojin Chung, Jin-Haeng |
author_sort | Park, Eunhyang |
collection | PubMed |
description | Cancer stem cells (CSCs) are a small subset of tumor cells that exhibit stem cell-like properties and contribute in treatment failure. To clarify the expression and prognostic significance of several CSC markers in non-small cell lung cancer, we retrospectively analyzed 368 patients with adenocarcinoma (n = 226) or squamous cell carcinoma (n = 142). We correlated the expression of six CSC markers – CD133, CD44, aldehyde dehydrogenase 1 (ALDH1), sex determining region Y-box 2 (SOX2), octamer binding transcription factor 4 (OCT4), and Nanog – with clinicopathologic and molecular variables and survival outcomes. In adenocarcinoma, CD133, ALDH1 and CD44 expression was associated with low pathologic stage and absence of lymphovascular invasion, while Nanog expression correlated with high histologic grade, lymphatic invasion and increased expression of Snail-1, a transcription factor associated with epithelial-mesenchymal transition. CSC marker expression was also associated with histologic subtypes in adenocarcinoma. Multivariate analysis showed that high Nanog expression was an independent factor associated with a poor prognosis in adenocarcinoma. CSC markers had no prognostic value in squamous cell carcinoma. These results suggest that Nanog is an independent negative prognostic factor that may be associated with epithelial-mesenchymal transition in lung adenocarcinoma. |
format | Online Article Text |
id | pubmed-5173151 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-51731512016-12-23 Prognostic significance of stem cell-related marker expression and its correlation with histologic subtypes in lung adenocarcinoma Park, Eunhyang Park, Soo Young Sun, Ping-Li Jin, Yan Kim, Ji Eun Jheon, Sanghoon Kim, Kwhanmien Lee, Choon Taek Kim, Hyojin Chung, Jin-Haeng Oncotarget Research Paper Cancer stem cells (CSCs) are a small subset of tumor cells that exhibit stem cell-like properties and contribute in treatment failure. To clarify the expression and prognostic significance of several CSC markers in non-small cell lung cancer, we retrospectively analyzed 368 patients with adenocarcinoma (n = 226) or squamous cell carcinoma (n = 142). We correlated the expression of six CSC markers – CD133, CD44, aldehyde dehydrogenase 1 (ALDH1), sex determining region Y-box 2 (SOX2), octamer binding transcription factor 4 (OCT4), and Nanog – with clinicopathologic and molecular variables and survival outcomes. In adenocarcinoma, CD133, ALDH1 and CD44 expression was associated with low pathologic stage and absence of lymphovascular invasion, while Nanog expression correlated with high histologic grade, lymphatic invasion and increased expression of Snail-1, a transcription factor associated with epithelial-mesenchymal transition. CSC marker expression was also associated with histologic subtypes in adenocarcinoma. Multivariate analysis showed that high Nanog expression was an independent factor associated with a poor prognosis in adenocarcinoma. CSC markers had no prognostic value in squamous cell carcinoma. These results suggest that Nanog is an independent negative prognostic factor that may be associated with epithelial-mesenchymal transition in lung adenocarcinoma. Impact Journals LLC 2016-06-07 /pmc/articles/PMC5173151/ /pubmed/27285762 http://dx.doi.org/10.18632/oncotarget.9894 Text en Copyright: © 2016 Park 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 Park, Eunhyang Park, Soo Young Sun, Ping-Li Jin, Yan Kim, Ji Eun Jheon, Sanghoon Kim, Kwhanmien Lee, Choon Taek Kim, Hyojin Chung, Jin-Haeng Prognostic significance of stem cell-related marker expression and its correlation with histologic subtypes in lung adenocarcinoma |
title | Prognostic significance of stem cell-related marker expression and its correlation with histologic subtypes in lung adenocarcinoma |
title_full | Prognostic significance of stem cell-related marker expression and its correlation with histologic subtypes in lung adenocarcinoma |
title_fullStr | Prognostic significance of stem cell-related marker expression and its correlation with histologic subtypes in lung adenocarcinoma |
title_full_unstemmed | Prognostic significance of stem cell-related marker expression and its correlation with histologic subtypes in lung adenocarcinoma |
title_short | Prognostic significance of stem cell-related marker expression and its correlation with histologic subtypes in lung adenocarcinoma |
title_sort | prognostic significance of stem cell-related marker expression and its correlation with histologic subtypes in lung adenocarcinoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5173151/ https://www.ncbi.nlm.nih.gov/pubmed/27285762 http://dx.doi.org/10.18632/oncotarget.9894 |
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