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Development and validation of a novel epigenetic-related prognostic signature and candidate drugs for patients with lung adenocarcinoma

Background: Epigenetic dysregulation has been increasingly proposed as a hallmark of cancer. Here, the aim of this study is to establish an epigenetic-related signature for predicting the prognosis of lung adenocarcinoma (LUAD) patients. Results: Five epigenetic-related genes (ERGs) (ARRB1, PARP1, P...

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Autores principales: Wang, Zhihao, Embaye, Kidane Siele, Yang, Qing, Qin, Lingzhi, Zhang, Chao, Liu, Liwei, Zhan, Xiaoqian, Zhang, Fengdi, Wang, Xi, Qin, Shenghui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8351720/
https://www.ncbi.nlm.nih.gov/pubmed/34285141
http://dx.doi.org/10.18632/aging.203315
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author Wang, Zhihao
Embaye, Kidane Siele
Yang, Qing
Qin, Lingzhi
Zhang, Chao
Liu, Liwei
Zhan, Xiaoqian
Zhang, Fengdi
Wang, Xi
Qin, Shenghui
author_facet Wang, Zhihao
Embaye, Kidane Siele
Yang, Qing
Qin, Lingzhi
Zhang, Chao
Liu, Liwei
Zhan, Xiaoqian
Zhang, Fengdi
Wang, Xi
Qin, Shenghui
author_sort Wang, Zhihao
collection PubMed
description Background: Epigenetic dysregulation has been increasingly proposed as a hallmark of cancer. Here, the aim of this study is to establish an epigenetic-related signature for predicting the prognosis of lung adenocarcinoma (LUAD) patients. Results: Five epigenetic-related genes (ERGs) (ARRB1, PARP1, PKM, TFDP1, and YWHAZ) were identified as prognostic hub genes and used to establish a prognostic signature. According our risk score system, LUAD patients were stratified into high and low risk groups, and patients in the high risk group had a worse prognosis. ROC analysis indicated that the signature was precise in predicting the prognosis. A new nomogram was constructed based on the five hub genes, which can predict the OS of every LUAD patients. The calibration curves showed that the nomogram had better accuracy in prediction. Finally, candidate drugs that aimed at hub ERGs were identified, which included 47 compounds. Conclusions: Our epigenetic-related signature nomogram can effectively and reliably predict OS of LUAD patients, also we provide precise targeted chemotherapeutic drugs. Methods: The genomic data and clinical data of LUAD cohort were downloaded from the TCGA database and ERGs were obtained from the EpiFactors database. GSE31210 and GSE50081 microarray datasets were included as independent external datasets. Univariate Cox, LASSO regression, and multivariate Cox analyses were applied to construct the epigenetic-related signature.
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spelling pubmed-83517202021-08-10 Development and validation of a novel epigenetic-related prognostic signature and candidate drugs for patients with lung adenocarcinoma Wang, Zhihao Embaye, Kidane Siele Yang, Qing Qin, Lingzhi Zhang, Chao Liu, Liwei Zhan, Xiaoqian Zhang, Fengdi Wang, Xi Qin, Shenghui Aging (Albany NY) Research Paper Background: Epigenetic dysregulation has been increasingly proposed as a hallmark of cancer. Here, the aim of this study is to establish an epigenetic-related signature for predicting the prognosis of lung adenocarcinoma (LUAD) patients. Results: Five epigenetic-related genes (ERGs) (ARRB1, PARP1, PKM, TFDP1, and YWHAZ) were identified as prognostic hub genes and used to establish a prognostic signature. According our risk score system, LUAD patients were stratified into high and low risk groups, and patients in the high risk group had a worse prognosis. ROC analysis indicated that the signature was precise in predicting the prognosis. A new nomogram was constructed based on the five hub genes, which can predict the OS of every LUAD patients. The calibration curves showed that the nomogram had better accuracy in prediction. Finally, candidate drugs that aimed at hub ERGs were identified, which included 47 compounds. Conclusions: Our epigenetic-related signature nomogram can effectively and reliably predict OS of LUAD patients, also we provide precise targeted chemotherapeutic drugs. Methods: The genomic data and clinical data of LUAD cohort were downloaded from the TCGA database and ERGs were obtained from the EpiFactors database. GSE31210 and GSE50081 microarray datasets were included as independent external datasets. Univariate Cox, LASSO regression, and multivariate Cox analyses were applied to construct the epigenetic-related signature. Impact Journals 2021-07-20 /pmc/articles/PMC8351720/ /pubmed/34285141 http://dx.doi.org/10.18632/aging.203315 Text en Copyright: © 2021 Wang et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (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, Zhihao
Embaye, Kidane Siele
Yang, Qing
Qin, Lingzhi
Zhang, Chao
Liu, Liwei
Zhan, Xiaoqian
Zhang, Fengdi
Wang, Xi
Qin, Shenghui
Development and validation of a novel epigenetic-related prognostic signature and candidate drugs for patients with lung adenocarcinoma
title Development and validation of a novel epigenetic-related prognostic signature and candidate drugs for patients with lung adenocarcinoma
title_full Development and validation of a novel epigenetic-related prognostic signature and candidate drugs for patients with lung adenocarcinoma
title_fullStr Development and validation of a novel epigenetic-related prognostic signature and candidate drugs for patients with lung adenocarcinoma
title_full_unstemmed Development and validation of a novel epigenetic-related prognostic signature and candidate drugs for patients with lung adenocarcinoma
title_short Development and validation of a novel epigenetic-related prognostic signature and candidate drugs for patients with lung adenocarcinoma
title_sort development and validation of a novel epigenetic-related prognostic signature and candidate drugs for patients with lung adenocarcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8351720/
https://www.ncbi.nlm.nih.gov/pubmed/34285141
http://dx.doi.org/10.18632/aging.203315
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