Identification and Validation of an 6-Metabolism-Related Gene Signature and Its Correlation With Immune Checkpoint in Hepatocellular Carcinoma
Hepatocellular carcinoma (HCC) is a common malignant tumor with relatively high malignancy and rapid disease progression. Metabolism-related genes (MRGs) are involved in the pathogenesis of HCC. This study explored potential key MRGs and their effect on T-cell immune function in the tumor immune mic...
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Frontiers Media S.A.
2021
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oai:doaj.org-article:277dc057036d488681d845b8a719c8ca2021-11-15T05:18:03ZIdentification and Validation of an 6-Metabolism-Related Gene Signature and Its Correlation With Immune Checkpoint in Hepatocellular Carcinoma2234-943X10.3389/fonc.2021.783934https://doaj.org/article/277dc057036d488681d845b8a719c8ca2021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fonc.2021.783934/fullhttps://doaj.org/toc/2234-943XHepatocellular carcinoma (HCC) is a common malignant tumor with relatively high malignancy and rapid disease progression. Metabolism-related genes (MRGs) are involved in the pathogenesis of HCC. This study explored potential key MRGs and their effect on T-cell immune function in the tumor immune microenvironment to provide new insight for the treatment of HCC. Of 456 differentially expressed MRGs identified from TCGA database, 21 were screened by MCODE and cytoHubba algorithms. From the key module, GAD1, SPP1, WFS1, GOT2, EHHADH, and APOA1 were selected for validation. The six MRGs were closely correlated with survival outcomes and clinicopathological characteristics in HCC. Receiver operating characteristics analysis and Kaplan-Meier plots showed that these genes had good prognostic value for HCC. Gene set enrichment analysis of the six MRGs indicated that they were associated with HCC development. TIMER and GEPIA databases revealed that WFS1 was significantly positively correlated and EHHADH was negatively correlated with tumor immune cell infiltration and immune checkpoint expression. Finally, quantificational real-time polymerase chain reaction (qRT-PCR) confirmed the expression of WFS1 and EHHADH mRNA in our own patients’ cohort samples and four HCC cell lines. Collectively, the present study identified six potential MRG biomarkers associated with the prognosis and tumor immune infiltration of HCC, thus providing new insight into the pathogenesis and treatment of HCC.He RenWanjing LiXin LiuShuliang LiShuliang LiShuliang LiHao GuoWei WangNa ZhaoFrontiers Media S.A.articlehepatocellular carcinomametabolism‐related genesprognosisimmune checkpointtumor infiltratingNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENFrontiers in Oncology, Vol 11 (2021) |
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hepatocellular carcinoma metabolism‐related genes prognosis immune checkpoint tumor infiltrating Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 |
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hepatocellular carcinoma metabolism‐related genes prognosis immune checkpoint tumor infiltrating Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 He Ren Wanjing Li Xin Liu Shuliang Li Shuliang Li Shuliang Li Hao Guo Wei Wang Na Zhao Identification and Validation of an 6-Metabolism-Related Gene Signature and Its Correlation With Immune Checkpoint in Hepatocellular Carcinoma |
description |
Hepatocellular carcinoma (HCC) is a common malignant tumor with relatively high malignancy and rapid disease progression. Metabolism-related genes (MRGs) are involved in the pathogenesis of HCC. This study explored potential key MRGs and their effect on T-cell immune function in the tumor immune microenvironment to provide new insight for the treatment of HCC. Of 456 differentially expressed MRGs identified from TCGA database, 21 were screened by MCODE and cytoHubba algorithms. From the key module, GAD1, SPP1, WFS1, GOT2, EHHADH, and APOA1 were selected for validation. The six MRGs were closely correlated with survival outcomes and clinicopathological characteristics in HCC. Receiver operating characteristics analysis and Kaplan-Meier plots showed that these genes had good prognostic value for HCC. Gene set enrichment analysis of the six MRGs indicated that they were associated with HCC development. TIMER and GEPIA databases revealed that WFS1 was significantly positively correlated and EHHADH was negatively correlated with tumor immune cell infiltration and immune checkpoint expression. Finally, quantificational real-time polymerase chain reaction (qRT-PCR) confirmed the expression of WFS1 and EHHADH mRNA in our own patients’ cohort samples and four HCC cell lines. Collectively, the present study identified six potential MRG biomarkers associated with the prognosis and tumor immune infiltration of HCC, thus providing new insight into the pathogenesis and treatment of HCC. |
format |
article |
author |
He Ren Wanjing Li Xin Liu Shuliang Li Shuliang Li Shuliang Li Hao Guo Wei Wang Na Zhao |
author_facet |
He Ren Wanjing Li Xin Liu Shuliang Li Shuliang Li Shuliang Li Hao Guo Wei Wang Na Zhao |
author_sort |
He Ren |
title |
Identification and Validation of an 6-Metabolism-Related Gene Signature and Its Correlation With Immune Checkpoint in Hepatocellular Carcinoma |
title_short |
Identification and Validation of an 6-Metabolism-Related Gene Signature and Its Correlation With Immune Checkpoint in Hepatocellular Carcinoma |
title_full |
Identification and Validation of an 6-Metabolism-Related Gene Signature and Its Correlation With Immune Checkpoint in Hepatocellular Carcinoma |
title_fullStr |
Identification and Validation of an 6-Metabolism-Related Gene Signature and Its Correlation With Immune Checkpoint in Hepatocellular Carcinoma |
title_full_unstemmed |
Identification and Validation of an 6-Metabolism-Related Gene Signature and Its Correlation With Immune Checkpoint in Hepatocellular Carcinoma |
title_sort |
identification and validation of an 6-metabolism-related gene signature and its correlation with immune checkpoint in hepatocellular carcinoma |
publisher |
Frontiers Media S.A. |
publishDate |
2021 |
url |
https://doaj.org/article/277dc057036d488681d845b8a719c8ca |
work_keys_str_mv |
AT heren identificationandvalidationofan6metabolismrelatedgenesignatureanditscorrelationwithimmunecheckpointinhepatocellularcarcinoma AT wanjingli identificationandvalidationofan6metabolismrelatedgenesignatureanditscorrelationwithimmunecheckpointinhepatocellularcarcinoma AT xinliu identificationandvalidationofan6metabolismrelatedgenesignatureanditscorrelationwithimmunecheckpointinhepatocellularcarcinoma AT shuliangli identificationandvalidationofan6metabolismrelatedgenesignatureanditscorrelationwithimmunecheckpointinhepatocellularcarcinoma AT shuliangli identificationandvalidationofan6metabolismrelatedgenesignatureanditscorrelationwithimmunecheckpointinhepatocellularcarcinoma AT shuliangli identificationandvalidationofan6metabolismrelatedgenesignatureanditscorrelationwithimmunecheckpointinhepatocellularcarcinoma AT haoguo identificationandvalidationofan6metabolismrelatedgenesignatureanditscorrelationwithimmunecheckpointinhepatocellularcarcinoma AT weiwang identificationandvalidationofan6metabolismrelatedgenesignatureanditscorrelationwithimmunecheckpointinhepatocellularcarcinoma AT nazhao identificationandvalidationofan6metabolismrelatedgenesignatureanditscorrelationwithimmunecheckpointinhepatocellularcarcinoma |
_version_ |
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