TABLE 6.
Studies on the therapeutic effects of quercetin in oral cancer.
| Type of Quercetin | Dose | Targets | Results | Model (in vitro/in vivo/Human) | Cell Line | Reference |
|---|---|---|---|---|---|---|
| Quercetin | 25–400 μM | NF-κB and matrix metalloproteinase-2/-9 | Inhibited migration and invasion | In vitro | SAS | Lai et al. (2013) |
| Quercetin | 10, 50, and 200 µM | SGLT1 and MRP2 | Induced apoptosis | In vitro | SCC-9 | Browning et al. (2005) |
| Quercetin | 10–100 µM | Blc2, Bax, and caspase 3 | G1 phase cell cycle arrest and induced mitochondrial apoptosis | In vitro | SCC25 | Chen et al. (2013) |
| Quercetin | 5–200 µM | Caspase-3, S-Phase, and TS enzyme | Induced necrosis and apoptosis | In vitro | SCC-9 | Haghiac and Walle (2005) |
| Quercetin | 0–50 µM | FOXO1 and EGFR | Growth arrest and apaptosis | In vitro and in vivo | HSC-3, TW206, and HGF | Huang et al. (2013) |
| Quercetin | 20, 40, and 80 µM | Anti-PARP antibody and caspase-3 | Induced apoptosis | In vitro | SCC-1483, SCC-25, and SCC-QLL1 | Kang et al. (2010) |
| Quercetin | 40 µM | ROS, caspase 3, 8, 9, Fas, Fas ligand, and ATF-6β | Induced morphological changes, decreased viability, and induced apoptosis | In vitro | SAS | Ma et al. (2018) |
| Quercetin | 100 mM | p38 MAPK–Hsp27, ABCG2, and MDR1 | Reduced tumor growth and decreased drug resistance | In vitro and in vivo | SCC25 | Chen et al. (2012) |
| Quercetin | 1–25 µM | cytochrome P450 and 1B1 | Chemopreventive agent | In vitro | SCC-9 | Walle and Walle (2007) |
| Quercetin | 25–100 µM | Bcl-2, Bax, and caspase-3 | Inhibited proliferation, inhibited migration and invasion, and induced apoptosis | In vitro | KB/VCR | Yuan et al. (2015) |
| Quercetin | 0, 50, and 100 µM | miR16 and HOXA10-axis | Inhibited viability and migration and invasion | In vitro | HSC-6, SCC-9, and hNOK | Zhao et al. (2019) |
| Quercetin | 10 μM | Cyclin A, E, PARP1, and Bax | Inhibited proliferation, cell cycle arrest, and DNA damage | In vitro | SCC-15 and Cal-33 | Singh et al. (2020) |