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Modulation of P-glycoprotein-mediated anticancer drug accumulation, cytotoxicity, and ATPase activity by flavonoid
Van H Tran1, Denese Marks, Rujee K Duke
1Faculty of Pharmacy, The University of Sydney, New South Wales, Australia.
Abstract:
Flavonoids are components of plant foods and of many herbal medicines taken in combination with anticancer drugs. We have examined the potential of flavonoids to affect the accumulation and cytotoxicity of 3 cytotoxic drugs [vinblastine (VLB), daunorubicin (DNR), and colchicine (COL)] that are substrates for the ABC transporter, P-glycoprotein in a vinblastine-resistant T-cell leukemia, CEM/VBL(100), that overexpresses P-glycoprotein. The effects of the flavonoids on accumulation and cytotoxicity of these drugs were different depending on the P-gp substrate used. Most of the 30 flavonoids tested decreased DNR accumulation in the VBL-resistant, but not sensitive, leukemia cells. By contrast, flavonoids that inhibited DNR accumulation enhanced the accumulation of fluorescently labeled vinblastine. None of these flavonoids affected COL accumulation. The effects of the flavonoids on the cytotoxicities of these drugs paralleled their effects on accumulation; the same flavonoids decreased DNR cytotoxicity but increased VLB cytotoxicity and had no effect on COL. Verapamil reversed the accumulation deficit and cytotoxicity of all three P-gp substrates. These effects correlated with the effects of flavonoids on P-gp-ATPase activity. Flavonoids that decreased DNR accumulation stimulated DNR-activated P-gp ATPase, whereas flavonoids that increased fluorescently labeled VLB accumulation inhibited VBL-stimulated P-gp ATPase activity, thereby accounting for the decrease or increase in cancer drug accumulation in resistant cells. We conclude that flavonoids often ingested by cancer patients may have different effects on anticancer drugs and that these findings should be considered in designing future combination treatments for cancer patients.
Insights
Flavonoids can alter how cancer drugs like daunorubicin and vinblastine work in resistant cells. Some flavonoids decrease daunorubicin accumulation and toxicity, while others increase vinblastine accumulation and toxicity.
Area of Science:
- Pharmacology
- Biochemistry
- Cancer Biology
Background:
- Flavonoids are plant compounds found in foods and herbal medicines.
- Many cancer patients use herbal medicines alongside chemotherapy.
- P-glycoprotein (P-gp) is an ABC transporter that confers multidrug resistance in cancer cells.
Purpose of the Study:
- To investigate how flavonoids affect the accumulation and cytotoxicity of P-gp substrate anticancer drugs.
- To understand the interaction between flavonoids and P-gp activity.
Main Methods:
- Tested 30 flavonoids on vinblastine-resistant T-cell leukemia (CEM/VBL(100)) overexpressing P-gp.
- Assessed the effects of flavonoids on the accumulation and cytotoxicity of vinblastine (VLB), daunorubicin (DNR), and colchicine (COL).
- Measured P-gp ATPase activity in the presence of flavonoids and P-gp substrates.
Main Results:
- Most flavonoids decreased DNR accumulation and cytotoxicity in resistant cells.
- Some flavonoids enhanced VLB accumulation and cytotoxicity.
- Flavonoids had no effect on COL accumulation or cytotoxicity.
- Effects on drug accumulation and cytotoxicity correlated with flavonoid modulation of P-gp ATPase activity.
Conclusions:
- Flavonoids can have differential effects on anticancer drug accumulation and efficacy, depending on the drug and flavonoid structure.
- These findings highlight the potential for drug-herb interactions in cancer therapy.
- Consideration of flavonoid interactions is crucial for designing effective combination cancer treatments.
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