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. 2017 Jun 6;8(33):55715–55730. doi: 10.18632/oncotarget.18382

Table 1. Genes most frequently mutated in hepatocellular carcinoma.

Pathways Genes Function Frequency in HCC (%) References
Telomere maintenance TERT Maintaining telomere length 47.1 [20]
Cell cycle control TP53 Tumor suppressor 28-36 [20, 29]
CCND1 Cell proliferation 7.2 [11]
CDKN2A Cell cycle regulator 7.2 [3]
WNT-β-catenin signaling CTNNB1 Transcriptional regulator 17-37 [20, 25, 33, 46]
AXIN1 Signal transducer 4-14 [20, 29]
Oxidative stress NFE2L2 Transcriptional regulator 6.4 [3]
KEAP1 Proteinase adaptor 8 [46]
Chromatin remodeling ARID1A Chromatin remodeling 16.8 [3]
ARID2 Chromatin remodeling 5.6 [3]
AKT-mTOR-MAPK pathway RPS6KA3 kinase 2-10 [3, 29]
PTEN Tumor suppressor 3 [25]
FGF19 Metabolic regulation factor 5 [25]
PI3KCA Effector of PTEN-AKT pathway 2-4 [3, 29]
JAK/STAT signaling JAK1 kinase 5 [20]
Angiogenesis VEGFA Tumor proliferation 3.8 [54]

ARID: AT-rich interaction domain; AXIN1: axin 1; CCND1: cyclin D1; CDKN2A: cyclin-dependent kinase inhibitor 2A; CTNNB1: β-catenin; FGF19: fibroblast growth factor 19; KEAP1: kelch like ECH associated protein 1; NFE2L2: nuclear factor, erythroid 2 like 2; PI3K: phosphoinositide 3-kinase; PTEN: phosphatase and tensin homologue; RPS6KA3: ribosomal protein S6 kinase 90kDa, polypeptide 3; TERT: telomerase reverse transcriptase; TP53: tumor protein p53; VEGFA: vascular endothelial growth factor A.