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

Abstract 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 dataset...

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Main Authors: Xiao‐Yan Sun, Shi‐Zhe Yu, Hua‐Peng Zhang, Jie Li, Wen‐Zhi Guo, Shui‐Jun Zhang
Format: Article
Language:English
Published: Wiley 2020-04-01
Series:Cancer Medicine
Subjects:
Online Access:https://doi.org/10.1002/cam4.2921
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author Xiao‐Yan Sun
Shi‐Zhe Yu
Hua‐Peng Zhang
Jie Li
Wen‐Zhi Guo
Shui‐Jun Zhang
author_facet Xiao‐Yan Sun
Shi‐Zhe Yu
Hua‐Peng Zhang
Jie Li
Wen‐Zhi Guo
Shui‐Jun Zhang
author_sort Xiao‐Yan Sun
collection DOAJ
description Abstract 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 (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 doaj.art-3424116fec5e42e1b96f61d9a6bcc9802022-12-21T17:33:08ZengWileyCancer Medicine2045-76342020-04-01982868287810.1002/cam4.2921A signature of 33 immune‐related gene pairs predicts clinical outcome in hepatocellular carcinomaXiao‐Yan Sun0Shi‐Zhe Yu1Hua‐Peng Zhang2Jie Li3Wen‐Zhi Guo4Shui‐Jun Zhang5Department of Hepatobiliary and Pancreatic Surgery The First Affiliated Hospital of Zhengzhou University Zhengzhou Henan ChinaDepartment of Hepatobiliary and Pancreatic Surgery The First Affiliated Hospital of Zhengzhou University Zhengzhou Henan ChinaDepartment of Hepatobiliary and Pancreatic Surgery The First Affiliated Hospital of Zhengzhou University Zhengzhou Henan ChinaDepartment of Hepatobiliary and Pancreatic Surgery The First Affiliated Hospital of Zhengzhou University Zhengzhou Henan ChinaDepartment of Hepatobiliary and Pancreatic Surgery The First Affiliated Hospital of Zhengzhou University Zhengzhou Henan ChinaDepartment of Hepatobiliary and Pancreatic Surgery The First Affiliated Hospital of Zhengzhou University Zhengzhou Henan ChinaAbstract 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 (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.https://doi.org/10.1002/cam4.2921gene pairsHCCprognosistumor immunology
spellingShingle Xiao‐Yan Sun
Shi‐Zhe Yu
Hua‐Peng Zhang
Jie Li
Wen‐Zhi Guo
Shui‐Jun Zhang
A signature of 33 immune‐related gene pairs predicts clinical outcome in hepatocellular carcinoma
Cancer Medicine
gene pairs
HCC
prognosis
tumor immunology
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 gene pairs
HCC
prognosis
tumor immunology
url https://doi.org/10.1002/cam4.2921
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