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Identification of differentially expressed genes in non-small cell lung cancer
Lung cancer is the most common malignant tumor and the leading cause of cancer-related deaths worldwide. Because current treatments for advanced non-small cell lung cancer (NSCLC), the most prevalent lung cancer histological subtype, show limited efficacy, screening for tumor-associated biomarkers u...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6932904/ https://www.ncbi.nlm.nih.gov/pubmed/31816603 http://dx.doi.org/10.18632/aging.102521 |
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author | Wang, Ke Chen, Ruo Feng, Zhuan Zhu, Yu-Meng Sun, Xiu-Xuan Huang, Wan Chen, Zhi-Nan |
author_facet | Wang, Ke Chen, Ruo Feng, Zhuan Zhu, Yu-Meng Sun, Xiu-Xuan Huang, Wan Chen, Zhi-Nan |
author_sort | Wang, Ke |
collection | PubMed |
description | Lung cancer is the most common malignant tumor and the leading cause of cancer-related deaths worldwide. Because current treatments for advanced non-small cell lung cancer (NSCLC), the most prevalent lung cancer histological subtype, show limited efficacy, screening for tumor-associated biomarkers using bioinformatics reflects the hope to improve early diagnosis and prognosis assessment. In our study, a Gene Expression Omnibus dataset was analyzed to identify genes with prognostic significance in NSCLC. Upon comparison with matched normal tissues, 118 differentially expressed genes (DEGs) were identified in NSCLC, and their functions were explored through bioinformatics analyses. The most significantly upregulated DEGs were TOP2A, SLC2A1, TPX2, and ASPM, all of which were significantly associated with poor overall survival (OS). Further analysis revealed that TOP2A had prognostic significance in early-stage lung cancer patients, and its expression correlated with levels of immune cell infiltration, especially dendritic cells (DCs). Our study provides a dataset of potentially prognostic NSCLC biomarkers, and highlights TOP2A as a valuable survival biomarker to improve prediction of prognosis in NSCLC. |
format | Online Article Text |
id | pubmed-6932904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-69329042020-01-03 Identification of differentially expressed genes in non-small cell lung cancer Wang, Ke Chen, Ruo Feng, Zhuan Zhu, Yu-Meng Sun, Xiu-Xuan Huang, Wan Chen, Zhi-Nan Aging (Albany NY) Research Paper Lung cancer is the most common malignant tumor and the leading cause of cancer-related deaths worldwide. Because current treatments for advanced non-small cell lung cancer (NSCLC), the most prevalent lung cancer histological subtype, show limited efficacy, screening for tumor-associated biomarkers using bioinformatics reflects the hope to improve early diagnosis and prognosis assessment. In our study, a Gene Expression Omnibus dataset was analyzed to identify genes with prognostic significance in NSCLC. Upon comparison with matched normal tissues, 118 differentially expressed genes (DEGs) were identified in NSCLC, and their functions were explored through bioinformatics analyses. The most significantly upregulated DEGs were TOP2A, SLC2A1, TPX2, and ASPM, all of which were significantly associated with poor overall survival (OS). Further analysis revealed that TOP2A had prognostic significance in early-stage lung cancer patients, and its expression correlated with levels of immune cell infiltration, especially dendritic cells (DCs). Our study provides a dataset of potentially prognostic NSCLC biomarkers, and highlights TOP2A as a valuable survival biomarker to improve prediction of prognosis in NSCLC. Impact Journals 2019-12-09 /pmc/articles/PMC6932904/ /pubmed/31816603 http://dx.doi.org/10.18632/aging.102521 Text en Copyright © 2019 Wang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Wang, Ke Chen, Ruo Feng, Zhuan Zhu, Yu-Meng Sun, Xiu-Xuan Huang, Wan Chen, Zhi-Nan Identification of differentially expressed genes in non-small cell lung cancer |
title | Identification of differentially expressed genes in non-small cell lung cancer |
title_full | Identification of differentially expressed genes in non-small cell lung cancer |
title_fullStr | Identification of differentially expressed genes in non-small cell lung cancer |
title_full_unstemmed | Identification of differentially expressed genes in non-small cell lung cancer |
title_short | Identification of differentially expressed genes in non-small cell lung cancer |
title_sort | identification of differentially expressed genes in non-small cell lung cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6932904/ https://www.ncbi.nlm.nih.gov/pubmed/31816603 http://dx.doi.org/10.18632/aging.102521 |
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