Department of Radiology, Institute of Green Nanotechnology, University of Missouri, Columbia, MO, 65212, USA.
Department of Radiation Oncology, Washington University School of Medicine, 4511 Forest Park Ave, St. Louis, MO, 63108, USA.
Sci Rep. 2021 Aug 18;11(1):16797. doi: 10.1038/s41598-021-96224-8.
Men with castration-resistant prostate cancer (CRPC) face poor prognosis and increased risk of treatment-incurred adverse effects resulting in one of the highest mortalities among patient population globally. Immune cells act as double-edged sword depending on the tumor microenvironment, which leads to increased infiltration of pro-tumor (M2) macrophages. Development of new immunomodulatory therapeutic agents capable of targeting the tumor microenvironment, and hence orchestrating the transformation of pro-tumor M2 macrophages to anti-tumor M1, would substantially improve treatment outcomes of CRPC patients. We report, herein, Mangiferin functionalized gold nanoparticulate agent (MGF-AuNPs) and its immunomodulatory characteristics in treating prostate cancer. We provide evidence of immunomodulatory intervention of MGF-AuNPs in prostate cancers through observations of enhanced levels of anti-tumor cytokines (IL-12 and TNF-α) with concomitant reductions in the levels of pro-tumor cytokines (IL-10 and IL-6). In the MGF-AuNPs treated groups, IL-12 was elevated to ten-fold while TNF-α was elevated to about 50-fold, while IL-10 and IL-6 were reduced by two-fold. Ability of MGF-AuNPs to target splenic macrophages is invoked via targeting of NF-kB signaling pathway. Finally, therapeutic efficacy of MGF-AuNPs, in treating prostate cancer in vivo in tumor bearing mice, is described taking into consideration various immunomodulatory interventions triggered by this green nanotechnology-based nanomedicine agent.
去势抵抗性前列腺癌 (CRPC) 患者的预后较差,发生治疗相关不良反应的风险增加,导致全球患者死亡率最高。免疫细胞在肿瘤微环境中充当双刃剑,导致促肿瘤 (M2) 巨噬细胞的浸润增加。开发能够靶向肿瘤微环境的新型免疫调节治疗药物,从而协调促肿瘤 M2 巨噬细胞向抗肿瘤 M1 的转化,将极大地改善 CRPC 患者的治疗效果。我们在此报告 Mangiferin 功能化金纳米颗粒剂 (MGF-AuNPs) 及其在治疗前列腺癌中的免疫调节特性。我们通过观察抗肿瘤细胞因子 (IL-12 和 TNF-α) 水平的提高以及促肿瘤细胞因子 (IL-10 和 IL-6) 水平的降低,提供了 MGF-AuNPs 对前列腺癌进行免疫调节干预的证据。在 MGF-AuNPs 处理组中,IL-12 升高了十倍,TNF-α 升高了约 50 倍,而 IL-10 和 IL-6 降低了两倍。MGF-AuNPs 通过靶向 NF-κB 信号通路来靶向脾脏巨噬细胞的能力。最后,考虑到这种基于绿色纳米技术的纳米医学药物引发的各种免疫调节干预,描述了 MGF-AuNPs 在治疗荷瘤小鼠体内前列腺癌中的治疗效果。