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A gene-based survival score for lung adenocarcinoma by multiple transcriptional datasets analysis
BACKGROUND: Lung adenocarcinoma (LUAD) remains a crucial factor endangering human health. Gene-based clinical predictions could be of great help for cancer intervention strategies. Here, we tried to build a gene-based survival score (SS) for LUAD via analyzing multiple transcriptional datasets. METH...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603718/ https://www.ncbi.nlm.nih.gov/pubmed/33129284 http://dx.doi.org/10.1186/s12885-020-07473-1 |
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author | Xiong, Yanlu Lei, Jie Zhao, Jinbo Lu, Qiang Feng, Yangbo Qiao, Tianyun Xin, Shaowei Han, Yong Jiang, Tao |
author_facet | Xiong, Yanlu Lei, Jie Zhao, Jinbo Lu, Qiang Feng, Yangbo Qiao, Tianyun Xin, Shaowei Han, Yong Jiang, Tao |
author_sort | Xiong, Yanlu |
collection | PubMed |
description | BACKGROUND: Lung adenocarcinoma (LUAD) remains a crucial factor endangering human health. Gene-based clinical predictions could be of great help for cancer intervention strategies. Here, we tried to build a gene-based survival score (SS) for LUAD via analyzing multiple transcriptional datasets. METHODS: We first acquired differentially expressed genes between tumors and normal tissues from intersections of four LUAD datasets. Next, survival-related genes were preliminarily unscrambled by univariate Cox regression and further filtrated by LASSO regression. Then, we applied PCA to establish a comprehensive SS based on survival-related genes. Subsequently, we applied four independent LUAD datasets to evaluate prognostic prediction of SS. Moreover, we explored associations between SS and clinicopathological features. Furthermore, we assessed independent predictive value of SS by multivariate Cox analysis and then built prognostic models based on clinical stage and SS. Finally, we performed pathway enrichments analysis and investigated immune checkpoints expression underlying SS in four datasets. RESULTS: We established a 13 gene-based SS, which could precisely predict OS and PFS of LUAD. Close relations were elicited between SS and canonical malignant indictors. Furthermore, SS could serve as an independent risk factor for OS and PFS. Besides, the predictive efficacies of prognostic models were also reasonable (C-indexes: OS, 0.7; PFS, 0.7). Finally, we demonstrated enhanced cell proliferation and immune escape might account for high clinical risk of SS. CONCLUSIONS: We built a 13 gene-based SS for prognostic prediction of LUAD, which exhibited wide applicability and could contribute to LUAD management. |
format | Online Article Text |
id | pubmed-7603718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-76037182020-11-02 A gene-based survival score for lung adenocarcinoma by multiple transcriptional datasets analysis Xiong, Yanlu Lei, Jie Zhao, Jinbo Lu, Qiang Feng, Yangbo Qiao, Tianyun Xin, Shaowei Han, Yong Jiang, Tao BMC Cancer Research Article BACKGROUND: Lung adenocarcinoma (LUAD) remains a crucial factor endangering human health. Gene-based clinical predictions could be of great help for cancer intervention strategies. Here, we tried to build a gene-based survival score (SS) for LUAD via analyzing multiple transcriptional datasets. METHODS: We first acquired differentially expressed genes between tumors and normal tissues from intersections of four LUAD datasets. Next, survival-related genes were preliminarily unscrambled by univariate Cox regression and further filtrated by LASSO regression. Then, we applied PCA to establish a comprehensive SS based on survival-related genes. Subsequently, we applied four independent LUAD datasets to evaluate prognostic prediction of SS. Moreover, we explored associations between SS and clinicopathological features. Furthermore, we assessed independent predictive value of SS by multivariate Cox analysis and then built prognostic models based on clinical stage and SS. Finally, we performed pathway enrichments analysis and investigated immune checkpoints expression underlying SS in four datasets. RESULTS: We established a 13 gene-based SS, which could precisely predict OS and PFS of LUAD. Close relations were elicited between SS and canonical malignant indictors. Furthermore, SS could serve as an independent risk factor for OS and PFS. Besides, the predictive efficacies of prognostic models were also reasonable (C-indexes: OS, 0.7; PFS, 0.7). Finally, we demonstrated enhanced cell proliferation and immune escape might account for high clinical risk of SS. CONCLUSIONS: We built a 13 gene-based SS for prognostic prediction of LUAD, which exhibited wide applicability and could contribute to LUAD management. BioMed Central 2020-10-31 /pmc/articles/PMC7603718/ /pubmed/33129284 http://dx.doi.org/10.1186/s12885-020-07473-1 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Xiong, Yanlu Lei, Jie Zhao, Jinbo Lu, Qiang Feng, Yangbo Qiao, Tianyun Xin, Shaowei Han, Yong Jiang, Tao A gene-based survival score for lung adenocarcinoma by multiple transcriptional datasets analysis |
title | A gene-based survival score for lung adenocarcinoma by multiple transcriptional datasets analysis |
title_full | A gene-based survival score for lung adenocarcinoma by multiple transcriptional datasets analysis |
title_fullStr | A gene-based survival score for lung adenocarcinoma by multiple transcriptional datasets analysis |
title_full_unstemmed | A gene-based survival score for lung adenocarcinoma by multiple transcriptional datasets analysis |
title_short | A gene-based survival score for lung adenocarcinoma by multiple transcriptional datasets analysis |
title_sort | gene-based survival score for lung adenocarcinoma by multiple transcriptional datasets analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603718/ https://www.ncbi.nlm.nih.gov/pubmed/33129284 http://dx.doi.org/10.1186/s12885-020-07473-1 |
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