Table 3.
Anticancer effects of PC and its compounds.
Pharmacological effects | Mechanism | Extracts/compounds | Minimal active concentration/dose | Cancer | Reference |
---|---|---|---|---|---|
Anticancer activity | Initiated apoptosis and S-phase cell cycle arrest through impeding Akt/ ERK/EGFR pathways | PC dissolved in saline | 300 mg/kg | Osteosarcoma | Zhao, Pan et al. 2022 |
Inhibited the activity of human breast cancer and promoted apoptosis | Crude extract | IC50 = 31.18 ± 1.95 μg/mL | Breast cancer | Pan, Shi et al. 2019 | |
IC50 = 28.12 ± 1.07 μg/mL | Ovarian cancer | ||||
Anti-human oral cancer, stimulated caspase-9 and -3 activities | Ethanol extract | 50 μg/mL | Oral cancer | Wang, Horng et al. 2019 | |
Anti-laryngeal cancer and inhibited the PDGF/AKT signaling pathway | Polydatin | 2 μmol/L | Laryngeal cancer | Li et al. 2017 | |
Reduced mean tumor volume | 50 mg/kg | ||||
Anti-leukemia, induced S-phase cell cycle arrest, and upregulated cyclin D1 and Bcl-2 | Polydatin | IC50 (48 h) = 50 μmol/L | Acute leukemia | Wang, Luo et al. 2016 | |
Anti-leukemia and inhibited Akt/mTOR/p70S6K signaling pathway | Polydatin | IC50 (24 h) = 80 μmol/L | Acute leukemia | Luo et al. 2016 | |
Anti-cervical cancer and inhibited PI3K/AKT/mTOR pathway | Polydatin | 50 μmol/L | Cervical cancer | Pan et al. 2017 | |
Anti-hepatoma and inhibited AKT/NF-κB pathway | Polydatin | IC50 (72 h) = 34.89 mg/L | Lung cancer | Sun and Ye 2019 | |
Inhibited the proliferation of human breast cancer and downregulated VEGF and MMP-9 | Polydatin | 0.2 μmol/L | Breast cancer | Chen et al. 2017 | |
Anticancer activity | Induced phase S cell cycle arrest and downregulated CREB and cyclin D1 | Polydatin | 1.5 μmol/L | Breast cancer | Feng et al. 2019 |
Inhibited the proliferation of cells, downregulated the expression of Bcl-2 and upregulated Bax | Resveratrol | 25 μmol/L | Liver cancer | Gu et al. 2014 | |
Induced cell blockage at phase S | Resveratrol | 12.5 μmol/L | Liver cancer | Gu et al. 2015 | |
Decreased the survival rate of cells and rested the cells at the G0/G1 phase | Resveratrol | IC50 (24 h) = 127 μmol/L | Gastric cancer | Jing et al. 2016 | |
Anti-ovarian cancer, promoted FOXD3 expression, activated miR-199a, and suppresses the expression of TGF-β2 | Emodin | 20 μmol/L | Ovarian cancer | Song et al. 2018 | |
Increased accumulation of DOX in SMMC-7721/DOX cells | Rhein | 20 μmol/L | Liver cancer | Wu, Cao et al. 2019 | |
Inhibited human hepatoma cells activity | Resveratrol-4-O-d-(2′-galloyl)-glucopyranoside | 2.5 μmol/L | Liver cancer | Xie et al. 2014 | |
Reduced mean tumor volume and weight in mice | 10 mg/kg | ||||
Anti-hepatoma and inhibited STAT3 signaling | 2-Ethoxystypandrone | IC50 = 3.69 ± 0.51 μmol/L | Liver cancer | Li, Zhang et al. 2019 | |
IC50 = 5.58 ± 0.89 μmol/L | |||||
Induced death of tumor cells and inhibited STAT3 and NF-κB pathways | 2-Methoxystypandrone | 10 μmol/L | Cervical cancer, Breast Cancer, Glioma, Ovarian cancer, Prostate cancer, Lung cancer | Kuang et al. 2014 | |
Induced multiple forms of cell death in cancer cells and activated JNK/iNOS/NO pathways | 2-Methoxy-6-acetyl-7-methyl-juglone | IC50 < 5.5 μmol/L | Lung cancer, Melanoma, Breast cancer | Sun et al. 2016 |