Department of Pharmacy, Faculty of Pharmacy, Al-Zaytoonah University of Jordan, Amman 11733, Jordan.
Cell Therapy Center, The University of Jordan, Amman 11942, Jordan.
Int J Mol Sci. 2020 May 8;21(9):3320. doi: 10.3390/ijms21093320.
Conjugating drugs with gold nanoparticles (GNP) is a key strategy in cancer therapy. Herein, the potential inhibition of the phosphatidylinositol 3-kinase (PI3K)/Akt pathway, and other pathways of the MCF-7 cell-line, was investigated upon treatment with gold nanorods (GNR) conjugated with a PI3K inhibitor drug. The results revealed that the coupling of GNR with the drug drastically modulated the expression of PI3Kα at the gene and protein levels compared to the drug or GNR alone. The PI3Kα pathway is involved in tumor progression and development through the mediation of different mechanisms such as apoptosis, proliferation, and DNA damage. Treatment with the nanocomplex significantly affected the gene expression of several transcription factors responsible for cell growth and proliferation, apoptotic pathways, and cell cycle arrest. Furthermore, the gene expression of different regulatory proteins involved in cancer progression and immune responses were significantly modified upon treatment with the nanocomplex compared to the free drug or GNR alone.
将药物与金纳米粒子(GNP)结合是癌症治疗的关键策略。在此,通过用与 PI3K 抑制剂药物偶联的金纳米棒(GNR)处理,研究了 MCF-7 细胞系中磷酸肌醇 3-激酶(PI3K)/Akt 途径及其他途径的潜在抑制作用。结果表明,与药物偶联的 GNR 与单独的药物或 GNR 相比,在基因和蛋白质水平上显著调节了 PI3Kα 的表达。PI3Kα 途径通过不同的机制,如凋亡、增殖和 DNA 损伤,参与肿瘤的发生和发展。该纳米复合物的处理显著影响了负责细胞生长和增殖、凋亡途径和细胞周期阻滞的几个转录因子的基因表达。此外,与单独使用游离药物或 GNR 相比,该纳米复合物处理后,不同的调节蛋白的基因表达在癌症进展和免疫反应中也有显著改变。