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A signature of 33 immune‐related gene pairs predicts clinical outcome in hepatocellular carcinoma

OBJECTIVE: Hepatocellular carcinoma (HCC) has become the second most common tumor type that contributes to cancer‐related death worldwide. The study aimed to establish a robust immune‐related gene pair (IRGP) signature for predicting the prognosis of HCC patients. METHODS: Two RNA‐seq datasets (The...

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Autores principales: Sun, Xiao‐Yan, Yu, Shi‐Zhe, Zhang, Hua‐Peng, Li, Jie, Guo, Wen‐Zhi, Zhang, Shui‐Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7163092/
https://www.ncbi.nlm.nih.gov/pubmed/32068352
http://dx.doi.org/10.1002/cam4.2921
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author Sun, Xiao‐Yan
Yu, Shi‐Zhe
Zhang, Hua‐Peng
Li, Jie
Guo, Wen‐Zhi
Zhang, Shui‐Jun
author_facet Sun, Xiao‐Yan
Yu, Shi‐Zhe
Zhang, Hua‐Peng
Li, Jie
Guo, Wen‐Zhi
Zhang, Shui‐Jun
author_sort Sun, Xiao‐Yan
collection PubMed
description OBJECTIVE: Hepatocellular carcinoma (HCC) has become the second most common tumor type that contributes to cancer‐related death worldwide. The study aimed to establish a robust immune‐related gene pair (IRGP) signature for predicting the prognosis of HCC patients. METHODS: Two RNA‐seq datasets (The Cancer Genome Atlas Program and International Cancer Genome Consortium) and one microarray dataset (http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE14520) were included in this study. We used a series of immune‐related genes from the ImmPort database to construct gene pairs. Lasso penalized Cox proportional hazards regression was employed to develop the best prognostic signature. We assigned patients into two groups with low immune risk and high immune risk. Then, the prognostic ability of the signature was evaluated by a log‐rank test and a Cox proportional hazards regression model. RESULTS: After 1000 iterations, the 33‐immune gene pair model obtained the highest frequency. As a result, we chose the 33 immune gene pairs to establish the immune‐related prognostic signature. As we expected, the immune‐related signature accurately predicted the prognosis of HCC patients, and high‐risk groups showed poor prognosis in the training datasets and testing datasets as well as in the validation datasets. Furthermore, the immune‐related gene pair (IRGP) signature also showed higher predictive accuracy than three existing prognostic signatures. CONCLUSION: Our prognostic signature, which reflects the link between the immune microenvironment and HCC patient outcome, is promising for prognosis prediction in HCC.
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spelling pubmed-71630922020-04-20 A signature of 33 immune‐related gene pairs predicts clinical outcome in hepatocellular carcinoma Sun, Xiao‐Yan Yu, Shi‐Zhe Zhang, Hua‐Peng Li, Jie Guo, Wen‐Zhi Zhang, Shui‐Jun Cancer Med Cancer Biology OBJECTIVE: Hepatocellular carcinoma (HCC) has become the second most common tumor type that contributes to cancer‐related death worldwide. The study aimed to establish a robust immune‐related gene pair (IRGP) signature for predicting the prognosis of HCC patients. METHODS: Two RNA‐seq datasets (The Cancer Genome Atlas Program and International Cancer Genome Consortium) and one microarray dataset (http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE14520) were included in this study. We used a series of immune‐related genes from the ImmPort database to construct gene pairs. Lasso penalized Cox proportional hazards regression was employed to develop the best prognostic signature. We assigned patients into two groups with low immune risk and high immune risk. Then, the prognostic ability of the signature was evaluated by a log‐rank test and a Cox proportional hazards regression model. RESULTS: After 1000 iterations, the 33‐immune gene pair model obtained the highest frequency. As a result, we chose the 33 immune gene pairs to establish the immune‐related prognostic signature. As we expected, the immune‐related signature accurately predicted the prognosis of HCC patients, and high‐risk groups showed poor prognosis in the training datasets and testing datasets as well as in the validation datasets. Furthermore, the immune‐related gene pair (IRGP) signature also showed higher predictive accuracy than three existing prognostic signatures. CONCLUSION: Our prognostic signature, which reflects the link between the immune microenvironment and HCC patient outcome, is promising for prognosis prediction in HCC. John Wiley and Sons Inc. 2020-02-18 /pmc/articles/PMC7163092/ /pubmed/32068352 http://dx.doi.org/10.1002/cam4.2921 Text en © 2020 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Cancer Biology
Sun, Xiao‐Yan
Yu, Shi‐Zhe
Zhang, Hua‐Peng
Li, Jie
Guo, Wen‐Zhi
Zhang, Shui‐Jun
A signature of 33 immune‐related gene pairs predicts clinical outcome in hepatocellular carcinoma
title A signature of 33 immune‐related gene pairs predicts clinical outcome in hepatocellular carcinoma
title_full A signature of 33 immune‐related gene pairs predicts clinical outcome in hepatocellular carcinoma
title_fullStr A signature of 33 immune‐related gene pairs predicts clinical outcome in hepatocellular carcinoma
title_full_unstemmed A signature of 33 immune‐related gene pairs predicts clinical outcome in hepatocellular carcinoma
title_short A signature of 33 immune‐related gene pairs predicts clinical outcome in hepatocellular carcinoma
title_sort signature of 33 immune‐related gene pairs predicts clinical outcome in hepatocellular carcinoma
topic Cancer Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7163092/
https://www.ncbi.nlm.nih.gov/pubmed/32068352
http://dx.doi.org/10.1002/cam4.2921
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