阿霉素
基因沉默
药物输送
小干扰RNA
癌细胞
癌症研究
基因传递
三阴性乳腺癌
乳腺癌
材料科学
细胞凋亡
毒品携带者
化疗
遗传增强
癌症
内化
靶向给药
化学
细胞
纳米技术
医学
转染
生物化学
基因
内科学
作者
Cansu Ümran Tunç,Ömer Aydın
标识
DOI:10.1016/j.jddst.2022.103603
摘要
Combinational gene and chemo-therapy approach has been investigated for more effective treatment of cancer. In this report, we demonstrated a multifunctional carrier system based on gold nanoparticles (AuNPs) for co-delivery of siRNAs against Bcl-2, an anti-apoptotic gene, and doxorubicin (Dox), a well-known chemotherapy drug, to obtain enhanced treatment efficacy against advanced breast cancer. Bcl-2-siRNAs were attached to the surface of 13 nm AuNPs, and Dox was directly intercalated to the siRNA molecules without any need for complex chemical modifications or coating. Successful loading of both siRNA and Dox therapeutics to AuNPs and formation of multipurpose carrier system were demonstrated. Dox-loaded carrier system exhibited cytotoxic effect on triple-negative breast cancer (TNBC) cells and provided efficient drug internalization. Moreover, enhanced apoptosis and inhibition of cancer cell proliferation were achieved with dual delivery of Bcl-2 siRNA and Dox by the co-delivery AuNPs system. In addition, silencing of the Bcl-2 gene along with chemotherapy provided reduced colony formation and cell migration of breast cancer cells. In conclusion, inhibition of Bcl-2 expression increased the therapeutic activity of Dox on TNBC. Nevertheless, our nano-carrier system has also been tested against MCF7 cell line. Our results demonstrated that the prepared multifunctional delivery system presented an effective vehicle for simultaneous delivery of gene therapy and chemotherapy agents.
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