|
Types | Cell lines/mice/patients | Ginsenosides and compounds | Physiological effects | Related mechanisms | Refs. |
|
| SMMC-7721 cells | Rg3 and oxaliplatin | Inhibits proliferation and promotes apoptosis | Downregulates PCNA and cyclin D1-CDK4 compound | [48] |
| SK-Hep1, HepG2, A549, and H322 cells | 20(S)-Rg3 and doxorubicin | Inhibits autophagy | Changes in gene expression and activates of the CHOP transcription factor | [33] |
In vitro | HepG2 and Huh7 cells | 20(S)-ginsenoside Rg3 and Sorafenib | Suppresses proliferation and induces apoptosis | Modulates PTEN/Akt signaling pathway | [51] |
| HepG2 and Bel7404 cells | Ginsenoside Rg3 and sorafenib | Reduces cell viability, glucose consumption, and lactate levels | Regulates the HK2-mediated glycolysis and PI3K/Akt signaling pathway | [52] |
| HepG2 and Huh7 cells | 20(S)-ginsenoside Rg3 and sorafenib | Suppresses HCC cell proliferation and induces apoptosis | Modulates PTEN/Akt signaling pathway | [51] |
|
In vivo | C57BL/6 mice | Nanoparticle conjugation of ginsenoside Rg3 | Remodels of unbalanced gut microbiota and metabolism | N/A | [56] |
| C57BL/6 mice | Rg3, Ganoderma lucidum polysaccharide, and oridonin | Restores immune function, reduces angiogenesis, and retards proliferation | Inhibits the epidermal growth factor receptor EGFR/AKT/epidermal growth factor receptor/protein kinase B/GSK3 signaling pathway. | [57] |
|
In clinical | 371 HCC patients | Ginsenoside Rg3 and sorafenib | Reduces cell viability, glucose consumption, and lactate levels | Regulates the HK2-mediated glycolysis and PI3K/Akt signaling pathway | [52] |
| 18 RCTs with 1308 HCC patients | Ginsenosides and TACE | Continuously benefits the efficacy and safety of TACE in HCC treatment | N/A | [55] |
|