Identification and validation of a five-gene prognostic signature for hepatocellular carcinoma
Abstract Background ARID1A is a commonly mutated tumor suppressor gene found in all human cancer types, but its clinical significance, oncogenic functions, and relevant mechanisms in hepatocellular carcinoma (HCC) are not well understood. Objective We aimed to improving the prognosis risk classifica...
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doaj-fb24f053d70440afa2bdf1f3528aef242021-03-28T11:21:17ZengBMCWorld Journal of Surgical Oncology1477-78192021-03-0119111310.1186/s12957-021-02202-9Identification and validation of a five-gene prognostic signature for hepatocellular carcinomaHuibin Yang0Junyu Huo1Xin Li2Qingdao UniversityDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Qingdao Municipal Hospital of Qingdao UniversityDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Qingdao Municipal Hospital of Qingdao UniversityAbstract Background ARID1A is a commonly mutated tumor suppressor gene found in all human cancer types, but its clinical significance, oncogenic functions, and relevant mechanisms in hepatocellular carcinoma (HCC) are not well understood. Objective We aimed to improving the prognosis risk classification of HCC from the perspective of ARID1A mutations. Materials and methods We examined the interaction between ARID1A mutations and the overall survival via Kaplan-Meier survival analysis. We used gene set enrichment analysis (GSEA) to elucidate the influence of ARID1A mutations on signaling pathways. A prognostic model was constructed using LASSO and multivariate Cox regression analyses. A receiver operating characteristic (ROC) curve was used to estimate the performance and accuracy of the model. Results HCC patients with ARID1A mutations presented poor prognosis. By GSEA, we showed that genes upregulated by reactive oxygen species (ROS) and regulated by MYC were positively correlated with ARID1A mutations. A prognostic signature consisting of 5 genes (SRXN1, LDHA, TFDP1, PPM1G, and EIF2S1) was constructed in our research. The signature showed good performance in predicting overall survival (OS) for HCC patients by internal and external validation. Conclusion Our research proposed a novel and robust approach for the prognostic risk classification of HCC patients, and this approach may provide new insights to improve the treatment strategy of HCC.https://doi.org/10.1186/s12957-021-02202-9Hepatocellular carcinomaARID1A mutationsPrognosticSignature |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Huibin Yang Junyu Huo Xin Li |
spellingShingle |
Huibin Yang Junyu Huo Xin Li Identification and validation of a five-gene prognostic signature for hepatocellular carcinoma World Journal of Surgical Oncology Hepatocellular carcinoma ARID1A mutations Prognostic Signature |
author_facet |
Huibin Yang Junyu Huo Xin Li |
author_sort |
Huibin Yang |
title |
Identification and validation of a five-gene prognostic signature for hepatocellular carcinoma |
title_short |
Identification and validation of a five-gene prognostic signature for hepatocellular carcinoma |
title_full |
Identification and validation of a five-gene prognostic signature for hepatocellular carcinoma |
title_fullStr |
Identification and validation of a five-gene prognostic signature for hepatocellular carcinoma |
title_full_unstemmed |
Identification and validation of a five-gene prognostic signature for hepatocellular carcinoma |
title_sort |
identification and validation of a five-gene prognostic signature for hepatocellular carcinoma |
publisher |
BMC |
series |
World Journal of Surgical Oncology |
issn |
1477-7819 |
publishDate |
2021-03-01 |
description |
Abstract Background ARID1A is a commonly mutated tumor suppressor gene found in all human cancer types, but its clinical significance, oncogenic functions, and relevant mechanisms in hepatocellular carcinoma (HCC) are not well understood. Objective We aimed to improving the prognosis risk classification of HCC from the perspective of ARID1A mutations. Materials and methods We examined the interaction between ARID1A mutations and the overall survival via Kaplan-Meier survival analysis. We used gene set enrichment analysis (GSEA) to elucidate the influence of ARID1A mutations on signaling pathways. A prognostic model was constructed using LASSO and multivariate Cox regression analyses. A receiver operating characteristic (ROC) curve was used to estimate the performance and accuracy of the model. Results HCC patients with ARID1A mutations presented poor prognosis. By GSEA, we showed that genes upregulated by reactive oxygen species (ROS) and regulated by MYC were positively correlated with ARID1A mutations. A prognostic signature consisting of 5 genes (SRXN1, LDHA, TFDP1, PPM1G, and EIF2S1) was constructed in our research. The signature showed good performance in predicting overall survival (OS) for HCC patients by internal and external validation. Conclusion Our research proposed a novel and robust approach for the prognostic risk classification of HCC patients, and this approach may provide new insights to improve the treatment strategy of HCC. |
topic |
Hepatocellular carcinoma ARID1A mutations Prognostic Signature |
url |
https://doi.org/10.1186/s12957-021-02202-9 |
work_keys_str_mv |
AT huibinyang identificationandvalidationofafivegeneprognosticsignatureforhepatocellularcarcinoma AT junyuhuo identificationandvalidationofafivegeneprognosticsignatureforhepatocellularcarcinoma AT xinli identificationandvalidationofafivegeneprognosticsignatureforhepatocellularcarcinoma |
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1724200190786666496 |