TABLE 1.
Compounds | Combined compounds | Models | Dosage | Synergistic effects | Results | Ref. |
---|---|---|---|---|---|---|
CPT | Monomethylarsonous acid | MCF-7 cells | 15 μm + 1 μm | Promotes apoptosis | Increased Bax, Bak, and Caspase-9 | Zhang et al. (2015) |
Sal A | Doxorubicin | MCF-7/DOX cells | 10, 30 mg/kg + 8 mg/kg | Facilitates chemotherapy sensitivity | Decreased protein arginine methyl transferase 1 activity | Li et al. (2016) |
Paclitaxel | MCF-7/PTX cells | 3, 6, 12 μM + 1,000 nM | Facilitates chemotherapy sensitivity | Inhibited PI3K/Akt pathway | Cai et al. (2014) | |
Tan IIA | Doxorubicin | MCF-7/DOX cells | 0.02 mg/L + 2 μg/ml | Facilitates chemotherapy sensitivity | Decreased β-catenin nuclear translocation | Li et al. (2021) |
Paclitaxel | MCF-7 cells | 1–20 mM + 5–100 μM | Facilitates chemotherapy sensitivity | Decreased microtubule associated protein | Lin et al. (2018) | |
17-AAG | MCF-7 cells | 0.5–10 μM + 0.001–50 μM | Enhances antitumor efficacy | Inhibited total protein kinase C activity | Lv et al. (2018) | |
Fulvestrants | ZR-75-1 tumor xenografts | 30 mg/kg/d + 250 mg/kg/w | Enhances antitumor efficacy | Decreased tumor growth | He et al. (2019) | |
Doxorubicin | MCF-7/DOX cells | 20 μg/ml + 2 μg/ml | Facilitates chemotherapy sensitivity and reduces toxic side effects | Inhibited PTEN/Akt pathway | (Li and Lai, 2017; Li et al., 2019) | |
RA | Doxorubicin | MCF-7/DOX cells | 1.5, 15, 50 mΜ + 0.2 μM | Facilitates chemotherapy sensitivity | Inhibited MDM2 p53 binding protein homolog gene and increased zinc finger E-box binding homeobox 1 gene | Juskowiak et al. (2018) |
Paclitaxel | Ehrlich’s ascites carcinoma-induced Swiss albino mice | 100 mg/kg/d + 10 mg/kg, 3 times/w | Enhances antitumor efficacy | Decreased tumor growth | Mahmoud et al. (2021) |