Aged garlic extract potentiates doxorubicin cytotoxicity in human breast cancer cells
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Alkreathy, Huda Mohammed
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King Abdulaziz Univ, Fac Med, Dept Pharmacol, Jeddah, Saudi ArabiaKing Abdulaziz Univ, Fac Med, Dept Pharmacol, Jeddah, Saudi Arabia
Alkreathy, Huda Mohammed
[1
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AlShehri, Noura Farraj
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King Abdulaziz Univ, Fac Med, Dept Pharmacol, Jeddah, Saudi ArabiaKing Abdulaziz Univ, Fac Med, Dept Pharmacol, Jeddah, Saudi Arabia
AlShehri, Noura Farraj
[1
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Kamel, Fatemah Omer
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King Abdulaziz Univ, Fac Med, Dept Pharmacol, Jeddah, Saudi ArabiaKing Abdulaziz Univ, Fac Med, Dept Pharmacol, Jeddah, Saudi Arabia
Kamel, Fatemah Omer
[1
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Alghamdi, Ahmed Khalaf
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King Saud Bin Abdulaziz Univ Hlth Sci, Coll Med, Jeddah, Saudi ArabiaKing Abdulaziz Univ, Fac Med, Dept Pharmacol, Jeddah, Saudi Arabia
Alghamdi, Ahmed Khalaf
[3
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Esmat, Ahmed
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King Abdulaziz Univ, Fac Med, Dept Pharmacol, Jeddah, Saudi Arabia
Ain Shams Univ, Fac Pharm, Dept Pharmacol & Toxicol, Cairo 11566, EgyptKing Abdulaziz Univ, Fac Med, Dept Pharmacol, Jeddah, Saudi Arabia
Esmat, Ahmed
[1
,2
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Karim, Shahid
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King Abdulaziz Univ, Fac Med, Dept Pharmacol, Jeddah, Saudi ArabiaKing Abdulaziz Univ, Fac Med, Dept Pharmacol, Jeddah, Saudi Arabia
Karim, Shahid
[1
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机构:
[1] King Abdulaziz Univ, Fac Med, Dept Pharmacol, Jeddah, Saudi Arabia
[2] Ain Shams Univ, Fac Pharm, Dept Pharmacol & Toxicol, Cairo 11566, Egypt
[3] King Saud Bin Abdulaziz Univ Hlth Sci, Coll Med, Jeddah, Saudi Arabia
Purpose: To investigate the potential chemo-sensitizing effect of aged garlic extract (AGE) on doxorubicin (DOX) in breast cancer cells (MCF-7), and the possible underlying mechanisms. Methods: Human breast cancer cell line (MCF-7) was treated with AGE and DOX. The cytotoxic effects of AGE and DOX were investigated via cell cycle analysis and apoptosis induction, using flow cytometry. Mechanistic studies involved the determination of cellular uptake of DOX and p-glycoprotein (P-gp) activity. Results: Combined treatment of MCF7 cells with AGE and DOX produced no significant effect at AGE dose of 10 mg/mL. However, co-treatment with AGE at doses of 50 and 93 mg/mL enhanced the cytotoxicity of DOX on MCF-7 cells, with IC50 values of 0.962 and 0.999 mu M, respectively, when compared with 1.85 mu M DOX alone. Moreover, Annexin V-FITC and PI techniques showed that AGE significantly increased percentage of cells in late apoptosis. Besides, AGE-DOX treatment significantly increased cellular uptake of DOX and inhibited P-gp activity, when compared with DOX alone (p < 0.05). Conclusion: AGE enhances the cytotoxic effect of DOX on MCF-7 cells, most likely due to cell cycle distribution, stimulation of apoptosis, increased uptake of DOX by MCF7, and inhibition of P-gp activity.