Review Article

Mechanism Research and Application for Ginsenosides in the Treatment of Hepatocellular Carcinoma

Table 2

Combined applications of ginsenosides against hepatocellular carcinoma.

TypesCell lines/mice/patientsGinsenosides and compoundsPhysiological effectsRelated mechanismsRefs.

SMMC-7721 cellsRg3 and oxaliplatinInhibits proliferation and promotes apoptosisDownregulates PCNA and cyclin D1-CDK4 compound[48]
SK-Hep1, HepG2, A549, and H322 cells20(S)-Rg3 and doxorubicinInhibits autophagyChanges in gene expression and activates of the CHOP transcription factor[33]
In vitroHepG2 and Huh7 cells20(S)-ginsenoside Rg3 and SorafenibSuppresses proliferation and induces apoptosisModulates PTEN/Akt signaling pathway[51]
HepG2 and Bel7404 cellsGinsenoside Rg3 and sorafenibReduces cell viability, glucose consumption, and lactate levelsRegulates the HK2-mediated glycolysis and PI3K/Akt signaling pathway[52]
HepG2 and Huh7 cells20(S)-ginsenoside Rg3 and sorafenibSuppresses HCC cell proliferation and induces apoptosisModulates PTEN/Akt signaling pathway[51]

In vivoC57BL/6 miceNanoparticle conjugation of ginsenoside Rg3Remodels of unbalanced gut microbiota and metabolismN/A[56]
C57BL/6 miceRg3, Ganoderma lucidum polysaccharide, and oridoninRestores immune function, reduces angiogenesis, and retards proliferationInhibits the epidermal growth factor receptor EGFR/AKT/epidermal growth factor receptor/protein kinase B/GSK3 signaling pathway.[57]

In clinical371 HCC patientsGinsenoside Rg3 and sorafenibReduces cell viability, glucose consumption, and lactate levelsRegulates the HK2-mediated glycolysis and PI3K/Akt signaling pathway[52]
18 RCTs with 1308 HCC patientsGinsenosides and TACEContinuously benefits the efficacy and safety of TACE in HCC treatmentN/A[55]