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Novel Pt(IV) complexes to overcome multidrug resistance in gastric cancer by targeting P-glycoprotein
Xinguang Cao1, Rui Li2, Huihua Xiong3
1Department of Digestive Disease, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Abstract:
Systematic toxicity and drug resistance significantly limited FDA-approved platinum drugs for further clinical applications. In order to reverse the resistance (MDR) and enhance their anticancer efficiency, four Pt(IV) complexes (12-15) conjugating with P-glycoprotein (P-gp) inhibitors were designed and synthesized. Among them, complex 14 (IC50 = 3.37 μM) efficiently reversed cisplatin resistance in SGC-7901/CDDP cell line and increased selectivity index (6.9) against normal HL-7702 cell line. Detailed mechanisms in SGC-7901/CDDP cells assays revealed that complex 14 efficiently induced apoptosis via down-regulating expression of P-gp for enhanced intracellular uptake of platinum, arrested cells at G2/M phase, induced DNA damage and initiated mitochondrial apoptosis pathway. Further in vivo studies demonstrated that the enhanced accumulation of complex 14 contributed to tumor inhibition of 75.6% in SGC-7901/CDDP xenografts, which was much higher than cisplatin (25.9%) and oxaliplatin (43%). Moreover, the low systematic toxicity made 14 a potential novel P-gp-mediated MDR modulator.
Insights
New platinum(IV) complexes combat cancer drug resistance by inhibiting P-glycoprotein (P-gp). Complex 14 shows potent anticancer activity and low toxicity, offering a promising strategy against multidrug resistance (MDR).
Area of Science:
- Medicinal Chemistry
- Cancer Biology
- Pharmacology
Background:
- Platinum-based drugs are crucial cancer therapeutics but face limitations due to systematic toxicity and acquired multidrug resistance (MDR).
- P-glycoprotein (P-gp) overexpression is a major mechanism contributing to MDR, reducing intracellular drug accumulation and efficacy.
- Novel strategies are needed to overcome P-gp-mediated MDR and enhance the therapeutic index of platinum drugs.
Purpose of the Study:
- To design and synthesize novel platinum(IV) complexes conjugated with P-gp inhibitors to overcome MDR.
- To evaluate the efficacy of these complexes in reversing cisplatin resistance and enhancing anticancer activity.
- To elucidate the underlying mechanisms of action, including P-gp modulation, apoptosis induction, and in vivo tumor inhibition.
Main Methods:
- Synthesis and characterization of four Pt(IV) complexes (12-15) incorporating P-gp inhibitors.
- In vitro evaluation of cytotoxicity, drug resistance reversal in SGC-7901/CDDP cells, and selectivity index against normal HL-7702 cells.
- Mechanistic studies involving P-gp expression analysis, cell cycle arrest, DNA damage assessment, and mitochondrial apoptosis pathway activation.
- In vivo efficacy studies using SGC-7901/CDDP xenograft models to assess tumor inhibition and compare with cisplatin and oxaliplatin.
Main Results:
- Complex 14 demonstrated significant activity with an IC50 of 3.37 μM and a selectivity index of 6.9.
- Complex 14 effectively reversed cisplatin resistance in SGC-7901/CDDP cells by down-regulating P-gp expression, enhancing platinum uptake.
- Mechanistic studies revealed that complex 14 induced apoptosis, arrested cells at G2/M phase, caused DNA damage, and activated the mitochondrial pathway.
- In vivo studies showed complex 14 achieved 75.6% tumor inhibition in xenografts, outperforming cisplatin (25.9%) and oxaliplatin (43%).
Conclusions:
- Complex 14 is a potent P-gp-mediated MDR modulator with enhanced anticancer efficacy and reduced systematic toxicity.
- This novel Pt(IV) complex represents a promising therapeutic candidate for overcoming platinum drug resistance in cancer treatment.
- Targeting P-gp in conjunction with platinum chemotherapy offers a viable strategy to improve clinical outcomes for cancer patients.
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