HBV-infected hepatocellular carcinoma can be robustly classified into three clinically relevant subgroups by a novel analytical protocol

被引:3
作者
Cheng, Zhiwei [1 ]
Li, Leijie [1 ]
Zhang, Yuening [1 ]
Ren, Yongyong [3 ]
Gu, Jianlei [3 ]
Wang, Xinbo [1 ]
Zhao, Hongyu [2 ]
Lu, Hui [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Life Sci & Biotechnol, Dept Bioinformat & Biostat, Shanghai, Peoples R China
[2] Yale Univ, Dept Biostat, New Haven, CT 06520 USA
[3] Shanghai Jiao Tong Univ, Bioinformat, Shanghai, Peoples R China
基金
国家重点研发计划;
关键词
hepatocellular carcinoma; hepatitis B virus (HBV); consistent differentially expressed genes; robust molecular classification; prognosis; REGULATORY T-CELLS; PROTEOGENOMIC CHARACTERIZATION; CANCER; REPLICATION; IDENTIFICATION; BIOMARKERS; PROGNOSIS; DISCOVERY; COMPLEX; MODEL;
D O I
10.1093/bib/bbac601
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Liver cancer is the third leading cause of cancer-related death worldwide, and hepatocellular carcinoma (HCC) accounts for a relatively large proportion of all primary liver malignancies. Among the several known risk factors, hepatitis B virus (HBV) infection is one of the important causes of HCC. In this study, we demonstrated that the HBV-infected HCC patients could be robustly classified into three clinically relevant subgroups, i.e. Cluster1, Cluster2 and Cluster3, based on consistent differentially expressed mRNAs and proteins, which showed better generalization. The proposed three subgroups showed different molecular characteristics, immune microenvironment and prognostic survival characteristics. The Cluster1 subgroup had near-normal levels of metabolism-related proteins, low proliferation activity and good immune infiltration, which were associated with its good liver function, smaller tumor size, good prognosis, low alpha-fetoprotein (AFP) levels and lower clinical stage. In contrast, the Cluster3 subgroup had the lowest levels of metabolism-related proteins, which corresponded with its severe liver dysfunction. Also, high proliferation activity and poor immune microenvironment in Cluster3 subgroup were associated with its poor prognosis, larger tumor size, high AFP levels, high incidence of tumor thrombus and higher clinical stage. The characteristics of the Cluster2 subgroup were between the Cluster1 and Cluster3 groups. In addition, MCM2-7, RFC2-5, MSH2, MSH6, SMC2, SMC4, NCPAG and TOP2A proteins were significantly upregulated in the Cluster3 subgroup. Meanwhile, abnormally high phosphorylation levels of these proteins were associated with high levels of DNA repair, telomere maintenance and proliferative features. Therefore, these proteins could be identified as potential diagnostic and prognostic markers. In general, our research provided a novel analytical protocol and insights for the robust classification, treatment and prevention of HBV-infected HCC.
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页数:17
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