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Establishment and Validation of an Interferon-Stimulated Genes (ISGs) Prognostic Signature in Pan-cancer Patients: A Multicenter, Real-world Study

Our study aims at developing an interferon-stimulated genes (ISGs) signature that could predict overall survival (OS) in cancer patients, which enrolled a total of 5643 pan-cancer patients. Linear models for microarray data method analysis were conducted to identify the differentially expressed prog...

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Autores principales: Zhou, Zheng, Zheng, Yujia, Mo, Shaobo, Li, Shuofeng, Zheng, Xinlei, Wei, Ran, Fan, Tao, Chen, Tianli, Xiao, Chu, Li, Chunxiang, He, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9254476/
https://www.ncbi.nlm.nih.gov/pubmed/35813478
http://dx.doi.org/10.7150/ijbs.71385
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author Zhou, Zheng
Zheng, Yujia
Mo, Shaobo
Li, Shuofeng
Zheng, Xinlei
Wei, Ran
Fan, Tao
Chen, Tianli
Xiao, Chu
Li, Chunxiang
He, Jie
author_facet Zhou, Zheng
Zheng, Yujia
Mo, Shaobo
Li, Shuofeng
Zheng, Xinlei
Wei, Ran
Fan, Tao
Chen, Tianli
Xiao, Chu
Li, Chunxiang
He, Jie
author_sort Zhou, Zheng
collection PubMed
description Our study aims at developing an interferon-stimulated genes (ISGs) signature that could predict overall survival (OS) in cancer patients, which enrolled a total of 5643 pan-cancer patients. Linear models for microarray data method analysis were conducted to identify the differentially expressed prognostic genes in the global ISGs family. Time-dependent receiver operating characteristic (ROC) and Kaplan-Meier survival analysis were used to test the efficiency of a multi-gene signature in predicting the prognosis of pan-cancer patients. The prognostic performance and potential biological function of gene signature were verified by quantitative real-time PCR in a pan-cancer independent cohort. Three ISGs genes were finally identified to build a classifier, a specific risk score formula, with which patients were classified into the low- or high-risk groups. Time-dependent ROC analyses proved prognostic accuracy. Then, its prognostic value was validated in seven external validation series. A nomogram was constructed to guide the individualized treatment of patients with lung adenocarcinoma. Biological pathway and tumor immune infiltration analysis showed that the signature might cause poor prognosis by blocking NK cell activation. Finally, the signature in our centers was confirmed by real-time quantitative PCR. A robust ISGs-related feature was discovered to effectively classify pan-cancer patients into subgroups with different OS.
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spelling pubmed-92544762022-07-09 Establishment and Validation of an Interferon-Stimulated Genes (ISGs) Prognostic Signature in Pan-cancer Patients: A Multicenter, Real-world Study Zhou, Zheng Zheng, Yujia Mo, Shaobo Li, Shuofeng Zheng, Xinlei Wei, Ran Fan, Tao Chen, Tianli Xiao, Chu Li, Chunxiang He, Jie Int J Biol Sci Research Paper Our study aims at developing an interferon-stimulated genes (ISGs) signature that could predict overall survival (OS) in cancer patients, which enrolled a total of 5643 pan-cancer patients. Linear models for microarray data method analysis were conducted to identify the differentially expressed prognostic genes in the global ISGs family. Time-dependent receiver operating characteristic (ROC) and Kaplan-Meier survival analysis were used to test the efficiency of a multi-gene signature in predicting the prognosis of pan-cancer patients. The prognostic performance and potential biological function of gene signature were verified by quantitative real-time PCR in a pan-cancer independent cohort. Three ISGs genes were finally identified to build a classifier, a specific risk score formula, with which patients were classified into the low- or high-risk groups. Time-dependent ROC analyses proved prognostic accuracy. Then, its prognostic value was validated in seven external validation series. A nomogram was constructed to guide the individualized treatment of patients with lung adenocarcinoma. Biological pathway and tumor immune infiltration analysis showed that the signature might cause poor prognosis by blocking NK cell activation. Finally, the signature in our centers was confirmed by real-time quantitative PCR. A robust ISGs-related feature was discovered to effectively classify pan-cancer patients into subgroups with different OS. Ivyspring International Publisher 2022-05-21 /pmc/articles/PMC9254476/ /pubmed/35813478 http://dx.doi.org/10.7150/ijbs.71385 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Zhou, Zheng
Zheng, Yujia
Mo, Shaobo
Li, Shuofeng
Zheng, Xinlei
Wei, Ran
Fan, Tao
Chen, Tianli
Xiao, Chu
Li, Chunxiang
He, Jie
Establishment and Validation of an Interferon-Stimulated Genes (ISGs) Prognostic Signature in Pan-cancer Patients: A Multicenter, Real-world Study
title Establishment and Validation of an Interferon-Stimulated Genes (ISGs) Prognostic Signature in Pan-cancer Patients: A Multicenter, Real-world Study
title_full Establishment and Validation of an Interferon-Stimulated Genes (ISGs) Prognostic Signature in Pan-cancer Patients: A Multicenter, Real-world Study
title_fullStr Establishment and Validation of an Interferon-Stimulated Genes (ISGs) Prognostic Signature in Pan-cancer Patients: A Multicenter, Real-world Study
title_full_unstemmed Establishment and Validation of an Interferon-Stimulated Genes (ISGs) Prognostic Signature in Pan-cancer Patients: A Multicenter, Real-world Study
title_short Establishment and Validation of an Interferon-Stimulated Genes (ISGs) Prognostic Signature in Pan-cancer Patients: A Multicenter, Real-world Study
title_sort establishment and validation of an interferon-stimulated genes (isgs) prognostic signature in pan-cancer patients: a multicenter, real-world study
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9254476/
https://www.ncbi.nlm.nih.gov/pubmed/35813478
http://dx.doi.org/10.7150/ijbs.71385
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