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Survival-related risk score of lung adenocarcinoma identified by weight gene co-expression network analysis

The present study aimed to identify the novel biomarkers and underlying molecular mechanisms of lung adenocarcinoma (LAC) to aid in its diagnosis, prognosis, prediction, disease monitoring and emerging therapies. Data from a total of 498 LAC samples were collected from The Cancer Genome Atlas and di...

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Autores principales: Wang, He, Lu, Di, Liu, Xiguang, Jiang, Jianjun, Feng, Siyang, Dong, Xiaoying, Shi, Xiaoshun, Wu, Hua, Xiong, Gang, Wang, Haofei, Cai, Kaican
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6781564/
https://www.ncbi.nlm.nih.gov/pubmed/31611953
http://dx.doi.org/10.3892/ol.2019.10795
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author Wang, He
Lu, Di
Liu, Xiguang
Jiang, Jianjun
Feng, Siyang
Dong, Xiaoying
Shi, Xiaoshun
Wu, Hua
Xiong, Gang
Wang, Haofei
Cai, Kaican
author_facet Wang, He
Lu, Di
Liu, Xiguang
Jiang, Jianjun
Feng, Siyang
Dong, Xiaoying
Shi, Xiaoshun
Wu, Hua
Xiong, Gang
Wang, Haofei
Cai, Kaican
author_sort Wang, He
collection PubMed
description The present study aimed to identify the novel biomarkers and underlying molecular mechanisms of lung adenocarcinoma (LAC) to aid in its diagnosis, prognosis, prediction, disease monitoring and emerging therapies. Data from a total of 498 LAC samples were collected from The Cancer Genome Atlas and divided into two sets by stratified randomization based on pathological Tumor-Node-Metastasis stage. The training set was comprised of 348 samples and the validation set was comprised of 150 samples. A total of 123 samples from the training set for patients who completed follow-up were analyzed by weighted gene co-expression network analysis. A module was identified that contained 113 protein-coding genes that were positively associated with overall survival (OS). A least absolute shrinkage and selection operator (LASSO) Cox regression model was constructed and four survival-associated genes (OPN3, GALNT2, FAM83A and KYNU) were retained. Risk score, calculated by the linear combination of each gene expression multiplied by the LASSO coefficient, could successfully discriminate between patients with LAC exhibiting low and high OS time in both sets. The results from the present study indicate that this risk score may contribute to potential diagnostic and therapeutic strategies for LAC management.
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spelling pubmed-67815642019-10-14 Survival-related risk score of lung adenocarcinoma identified by weight gene co-expression network analysis Wang, He Lu, Di Liu, Xiguang Jiang, Jianjun Feng, Siyang Dong, Xiaoying Shi, Xiaoshun Wu, Hua Xiong, Gang Wang, Haofei Cai, Kaican Oncol Lett Articles The present study aimed to identify the novel biomarkers and underlying molecular mechanisms of lung adenocarcinoma (LAC) to aid in its diagnosis, prognosis, prediction, disease monitoring and emerging therapies. Data from a total of 498 LAC samples were collected from The Cancer Genome Atlas and divided into two sets by stratified randomization based on pathological Tumor-Node-Metastasis stage. The training set was comprised of 348 samples and the validation set was comprised of 150 samples. A total of 123 samples from the training set for patients who completed follow-up were analyzed by weighted gene co-expression network analysis. A module was identified that contained 113 protein-coding genes that were positively associated with overall survival (OS). A least absolute shrinkage and selection operator (LASSO) Cox regression model was constructed and four survival-associated genes (OPN3, GALNT2, FAM83A and KYNU) were retained. Risk score, calculated by the linear combination of each gene expression multiplied by the LASSO coefficient, could successfully discriminate between patients with LAC exhibiting low and high OS time in both sets. The results from the present study indicate that this risk score may contribute to potential diagnostic and therapeutic strategies for LAC management. D.A. Spandidos 2019-11 2019-09-04 /pmc/articles/PMC6781564/ /pubmed/31611953 http://dx.doi.org/10.3892/ol.2019.10795 Text en Copyright: © Wang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Wang, He
Lu, Di
Liu, Xiguang
Jiang, Jianjun
Feng, Siyang
Dong, Xiaoying
Shi, Xiaoshun
Wu, Hua
Xiong, Gang
Wang, Haofei
Cai, Kaican
Survival-related risk score of lung adenocarcinoma identified by weight gene co-expression network analysis
title Survival-related risk score of lung adenocarcinoma identified by weight gene co-expression network analysis
title_full Survival-related risk score of lung adenocarcinoma identified by weight gene co-expression network analysis
title_fullStr Survival-related risk score of lung adenocarcinoma identified by weight gene co-expression network analysis
title_full_unstemmed Survival-related risk score of lung adenocarcinoma identified by weight gene co-expression network analysis
title_short Survival-related risk score of lung adenocarcinoma identified by weight gene co-expression network analysis
title_sort survival-related risk score of lung adenocarcinoma identified by weight gene co-expression network analysis
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6781564/
https://www.ncbi.nlm.nih.gov/pubmed/31611953
http://dx.doi.org/10.3892/ol.2019.10795
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