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载柔红霉素的 Fe3O4 磁性纳米粒子克服多药耐药并诱导体内 K562-n/VCR 细胞凋亡。

Daunorubicin-loaded magnetic nanoparticles of Fe3O4 overcome multidrug resistance and induce apoptosis of K562-n/VCR cells in vivo.

机构信息

Department of Hematology.

出版信息

Int J Nanomedicine. 2009;4:201-8. doi: 10.2147/ijn.s7287. Epub 2009 Oct 19.

Abstract

Multidrug resistance (MDR) is a major obstacle to cancer chemotherapy. We evaluated the effect of daunorubicin (DNR)-loaded magnetic nanoparticles of Fe3O4 (MNPs-Fe3O4) on K562-n/VCR cells in vivo. K562-n and its MDR counterpart K562-n/VCR cell were inoculated into nude mice subcutaneously. The mice were randomly divided into four groups: group A received normal saline, group B received DNR, group C received MNPs-Fe3O4, and group D received DNR-loaded MNPs-Fe3O4. For K562-n/VCR tumor, the weight was markedly lower in group D than that in groups A, B, and C. The transcriptions of Mdr-1 and Bcl-2 gene were significantly lower in group D than those in groups A, B, and C. The expression of Bcl-2 was lower in group D than those in groups A, B, and C, but there was no difference in the expression of P-glycoprotein. The transcriptions and expressions of Bax and caspase-3 in group D were increased significantly when compared with groups A, B, and C. In conclusion, DNR-loaded MNPs-Fe3O4 can overcome MDR in vivo.

摘要

多药耐药(MDR)是癌症化疗的主要障碍。我们评估了载柔红霉素(DNR)的四氧化三铁(MNPs-Fe3O4)磁性纳米粒子对体内 K562-n/VCR 细胞的影响。将 K562-n 和其多药耐药对应物 K562-n/VCR 细胞皮下接种到裸鼠中。将小鼠随机分为四组:A 组接受生理盐水,B 组接受 DNR,C 组接受 MNPs-Fe3O4,D 组接受载 DNR 的 MNPs-Fe3O4。对于 K562-n/VCR 肿瘤,D 组的重量明显低于 A、B 和 C 组。D 组的 Mdr-1 和 Bcl-2 基因转录明显低于 A、B 和 C 组。D 组的 Bcl-2 表达低于 A、B 和 C 组,但 P-糖蛋白的表达没有差异。与 A、B 和 C 组相比,D 组 Bax 和 caspase-3 的转录和表达显著增加。总之,载 DNR 的 MNPs-Fe3O4 可以在体内克服 MDR。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e418/2775690/ae734823b90b/ijn-4-201f1.jpg

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