Enhanced Cytotoxic Effect of Doxorubicin Conjugated to Glutathione-Stabilized Gold Nanoparticles in Canine Osteosarcoma-In Vitro Studies

被引:14
作者
Malek, Anna [1 ]
Taciak, Bartlomiej [2 ]
Sobczak, Katarzyna [3 ]
Grzelak, Agnieszka [3 ]
Wojcik, Michal [3 ]
Mieczkowski, Jozef [3 ]
Lechowski, Roman [1 ]
Zabielska-Koczywas, Katarzyna A. [1 ]
机构
[1] Warsaw Univ Life Sci, Inst Vet Med, Dept Small Anim Dis & Clin, Nowoursynowska 159c, PL-02776 Warsaw, Poland
[2] Warsaw Univ Life Sci, Inst Biol, Dept Canc Biol, Nowoursynowska 159, PL-02776 Warsaw, Poland
[3] Univ Warsaw, Fac Chem, Lab Organ Nanomat & Biomol, Pasteura 1, PL-02093 Warsaw, Poland
关键词
dogs; doxorubicin; flow cytometry; gold; humans; nanoparticles; osteosarcoma; P-glycoprotein; MULTIDRUG-RESISTANCE MDR; P-GLYCOPROTEIN; DRUG-RESISTANCE; PHASE-I; DOGS; CANCER; TUMORS; THERAPY; EFFLUX; IMMUNOTHERAPY;
D O I
10.3390/molecules26123487
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Osteosarcoma (OSA) is the most common malignant bone neoplasia in humans and dogs. In dogs, treatment consists of surgery in combination with chemotherapy (mostly carboplatin and/or doxorubicin (Dox)). Chemotherapy is often rendered ineffective by multidrug resistance. Previous studies have revealed that Dox conjugated with 4 nm glutathione-stabilized gold nanoparticles (Au-GSH-Dox) enhanced the anti-tumor activity and cytotoxicity of Dox in Dox-resistant feline fibrosarcoma cell lines exhibiting high P-glycoprotein (P-gp) activity. The present study investigated the influence of Au-GSH-Dox on the canine OSA cell line D17 and its relationship with P-gp activity. A human Dox-sensitive OSA cell line, U2OS, served as the negative control. Au-GSH-Dox, compared to free Dox, presented a greater cytotoxic effect on D17 (IC50 values for Au-GSH-Dox and Dox were 7.9 mu g/mL and 15.2 mu g/mL, respectively) but not on the U2OS cell line. All concentrations of Au-GSH (ranging from 10 to 1000 mu g/mL) were non-toxic in both cell lines. Inhibition of the D17 cell line with 100 mu M verapamil resulted in an increase in free Dox but not in intracellular Au-GSH-Dox. The results indicate that Au-GSH-Dox may act as an effective drug in canine OSA by bypassing P-gp.
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页数:16
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