Research Article

Investigating Pathogenic and Hepatocarcinogenic Mechanisms from Normal Liver to HCC by Constructing Genetic and Epigenetic Networks via Big Genetic and Epigenetic Data Mining and Genome-Wide NGS Data Identification

Table 1

Network biomarkers for preventing the hepatocarcinogenesis of NAFLD&NASH and PBC&PSC.

NAFLD&NASH to HCCPBC&PSC to HCC

The highly activated network biomarkers for potential inhibition strategy of drug designACTA2, AIFM1, APP, EGFR, GRB2, NEDD8, SHC1, TUBA1C, TUBB6, IL4R, GPR37, FRAT2, HIST2H2BE, HSPB1, ZNF480, TIMP1, ALDOB, ZYX, YBX1, TP53, STAT5A, AR, TELO2, PXN, TBP, REPIN1, HSF1, ETS1, STUB1, RFC5, RPL30, TRMT1, GSK3B, UBC, ALB, and MIR21ACTB, ADRB2, APP, CSNK2A1, EGFR, HUWE1, LMNB1, PCK1, PPP2CA, SMAD5, TSC22D1, ESR1, PGR, RYR2, FRAT2, HIST2H2BE, ZNF480, H3F3A, TIMP1, ALDOB, IGF2, AR, TP53, SRF, NRF1, STAT5A, RPL23A, SP1, SP3, CEBPA, BPTF, ETS1, MDC1, RFC5, RPL30, TRMT1, UBC, GSK3B, TF, and MIR21
The repressed network biomarkers for potential activation strategy of drug designALK and GATA1CEBPE and GATA1