Hypoxia-based classification and prognostic signature for clinical management of hepatocellular carcinoma

Abstract Objective Intratumoral hypoxia is an essential feature of hepatocellular carcinoma (HCC). Herein, we investigated the hypoxia-based heterogeneity and relevant clinical implication in HCC. Methods Three HCC cohorts: TCGA-LIHC, LICA-FR, and LIRI-JP were retrospectively gathered. Consensus clu...

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Main Authors: Ke Li, Yanfang Yang, Mingwei Ma, Suping Lu, Junjie Li
Format: Article
Language:English
Published: BMC 2023-07-01
Series:World Journal of Surgical Oncology
Subjects:
Online Access:https://doi.org/10.1186/s12957-023-03090-x
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author Ke Li
Yanfang Yang
Mingwei Ma
Suping Lu
Junjie Li
author_facet Ke Li
Yanfang Yang
Mingwei Ma
Suping Lu
Junjie Li
author_sort Ke Li
collection DOAJ
description Abstract Objective Intratumoral hypoxia is an essential feature of hepatocellular carcinoma (HCC). Herein, we investigated the hypoxia-based heterogeneity and relevant clinical implication in HCC. Methods Three HCC cohorts: TCGA-LIHC, LICA-FR, and LIRI-JP were retrospectively gathered. Consensus clustering analysis was utilized for hypoxia-based classification based upon transcriptome of hypoxia genes. Through LASSO algorithm, a hypoxia-relevant prognostic signature was built. Immunotherapeutic response was inferred through analyzing immune checkpoints, T cell inflamed score, TIDE score, and TMB score. RNF145 expression was measured in normoxic or hypoxic HCC cells. In RNF145-knockout cells, CCK-8, TUNEL, and scratch tests were implemented. Results HCC patients were classified into two hypoxia subtypes, with more advanced stages and poorer prognosis in cluster2 than cluster1. The heterogeneity in tumor infiltrating immune cells and genetic mutation was found between subtypes. The hypoxia-relevant prognostic model was proposed, composed of ANLN, CBX2, DLGAP5, FBLN2, FTCD, HMOX1, IGLV1-44, IL33, LCAT, LPCAT1, MKI67, PFN2, RNF145, S100A9, and SPP1). It was predicted that high-risk patients presented worse prognosis with an independent and reliable manner. Based upon high expression of immune checkpoints (CD209, CTLA4, HAVCR2, SIRPA, TNFRSF18, TNFRSF4, and TNFRSF9), high T cell inflamed score, low TIDE score and high TMB score, high-risk patients might respond to immunotherapy. Experimental validation showed that RNF145 was upregulated in hypoxic HCC cells, RNF145 knockdown attenuated proliferation and migration, but aggravated apoptosis in HCC cells. Conclusion Altogether, the hypoxia-based classification and prognostic signature might be useful for prognostication and guiding treatment of HCC.
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spelling doaj.art-abf0cbdf2fb046dab53797274055af142023-07-23T11:16:13ZengBMCWorld Journal of Surgical Oncology1477-78192023-07-0121111710.1186/s12957-023-03090-xHypoxia-based classification and prognostic signature for clinical management of hepatocellular carcinomaKe Li0Yanfang Yang1Mingwei Ma2Suping Lu3Junjie Li4Ruigu Medical Laboratory of Guangxi Medical University Co., LTDGuangxi Zhuoqiang Technology Co. LTDThe First Affiliated Hospital of Guangxi Medical UniversityForesea Life Insurance Nanning HospitalGuangxi Zhuoqiang Technology Co. LTDAbstract Objective Intratumoral hypoxia is an essential feature of hepatocellular carcinoma (HCC). Herein, we investigated the hypoxia-based heterogeneity and relevant clinical implication in HCC. Methods Three HCC cohorts: TCGA-LIHC, LICA-FR, and LIRI-JP were retrospectively gathered. Consensus clustering analysis was utilized for hypoxia-based classification based upon transcriptome of hypoxia genes. Through LASSO algorithm, a hypoxia-relevant prognostic signature was built. Immunotherapeutic response was inferred through analyzing immune checkpoints, T cell inflamed score, TIDE score, and TMB score. RNF145 expression was measured in normoxic or hypoxic HCC cells. In RNF145-knockout cells, CCK-8, TUNEL, and scratch tests were implemented. Results HCC patients were classified into two hypoxia subtypes, with more advanced stages and poorer prognosis in cluster2 than cluster1. The heterogeneity in tumor infiltrating immune cells and genetic mutation was found between subtypes. The hypoxia-relevant prognostic model was proposed, composed of ANLN, CBX2, DLGAP5, FBLN2, FTCD, HMOX1, IGLV1-44, IL33, LCAT, LPCAT1, MKI67, PFN2, RNF145, S100A9, and SPP1). It was predicted that high-risk patients presented worse prognosis with an independent and reliable manner. Based upon high expression of immune checkpoints (CD209, CTLA4, HAVCR2, SIRPA, TNFRSF18, TNFRSF4, and TNFRSF9), high T cell inflamed score, low TIDE score and high TMB score, high-risk patients might respond to immunotherapy. Experimental validation showed that RNF145 was upregulated in hypoxic HCC cells, RNF145 knockdown attenuated proliferation and migration, but aggravated apoptosis in HCC cells. Conclusion Altogether, the hypoxia-based classification and prognostic signature might be useful for prognostication and guiding treatment of HCC.https://doi.org/10.1186/s12957-023-03090-xHypoxiaHepatocellular carcinomaRNF145PrognosisGenetic mutationImmunotherapy
spellingShingle Ke Li
Yanfang Yang
Mingwei Ma
Suping Lu
Junjie Li
Hypoxia-based classification and prognostic signature for clinical management of hepatocellular carcinoma
World Journal of Surgical Oncology
Hypoxia
Hepatocellular carcinoma
RNF145
Prognosis
Genetic mutation
Immunotherapy
title Hypoxia-based classification and prognostic signature for clinical management of hepatocellular carcinoma
title_full Hypoxia-based classification and prognostic signature for clinical management of hepatocellular carcinoma
title_fullStr Hypoxia-based classification and prognostic signature for clinical management of hepatocellular carcinoma
title_full_unstemmed Hypoxia-based classification and prognostic signature for clinical management of hepatocellular carcinoma
title_short Hypoxia-based classification and prognostic signature for clinical management of hepatocellular carcinoma
title_sort hypoxia based classification and prognostic signature for clinical management of hepatocellular carcinoma
topic Hypoxia
Hepatocellular carcinoma
RNF145
Prognosis
Genetic mutation
Immunotherapy
url https://doi.org/10.1186/s12957-023-03090-x
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AT yanfangyang hypoxiabasedclassificationandprognosticsignatureforclinicalmanagementofhepatocellularcarcinoma
AT mingweima hypoxiabasedclassificationandprognosticsignatureforclinicalmanagementofhepatocellularcarcinoma
AT supinglu hypoxiabasedclassificationandprognosticsignatureforclinicalmanagementofhepatocellularcarcinoma
AT junjieli hypoxiabasedclassificationandprognosticsignatureforclinicalmanagementofhepatocellularcarcinoma