TABLE 1.
Tumor types and characteristics of various active components of ginseng.
| Type | Composition | Tumor type | Synergistic reaction | Features |
|---|---|---|---|---|
| Ginsenosides and Their Metabolites | Rb1, Rb2, Rb3、Rc, Rd, Rg3, Rg5, Rh2, Rs11, Rk1, F2, CK, Re, Re7, Rg1, Rg18, Rh1, Rh4, Rp1, Rf, F1, PPD, 25-OH-PPD, 25-OCH3-PPD | Esophageal, Stomach, Liver, Colon, Pancreas, and Gallbladder | Cisplatin, Docetaxel, Doxorubicin, Gemcitabine, Oxaliplatin, Sorafenib and 5-FU | ①Wide range of anti-tumor effects |
| Ginseng Polysaccharides | GFP1, PGP2a、PGPW1, Ginsan、WGPA-1-HG, 2-HG, 3-HG, 4-HG, WGPA-3-RG, 4-RG | Stomach, Liver, Colon | - | ②Anti-tumor components are complex and time- and dose-dependent |
| Ginseng Polyacetylenes | PND, PNT, PNN | Liver, Pancreas, and Colon | Gemcitabine | ③Anti-tumor effects are exerted through multiple pathways |
| Sterols | β-Sitosterl, Stigmasterol | Stomach, Liver, Colorectal, and Gallbladder | Cisplatin, Gemcitabine, Oxaliplatin and Paclitaxel | ④Synergistic effects can be produced in combination with multiple anti-tumor therapies to improve efficacy and reduce toxic side effects |
| Volatile Oils | β-Panasinsene | Stomach, Liver, Colorectal, Pancreas, and Bile Duct | Cetuximab, Doxorubicin, Erlotinib, Gefitinib, Oxaliplatin, Paclitaxel and 5-FU | ⑤Combined with novel drug delivery systems |
| α-Gurjunene, Germacrene | ||||
| β-Gurjunene | ||||
| β-Elemene | ||||
| β-Caryophyllene | ||||
| β-Neoclovene | ||||
| Organic Acids | Citric Acid, Cinnamic Acid, Fumaric Acid, Maleic Acid, Salicylic Acid | Liver, Colorecta | Cisplatin | ⑥Prevention of precancerous lesions |