Sulthana Shoukath, Banerjee Tuhina, Kallu Jyothi, Vuppala Sudershini Reddy, Heckert Blaze, Naz Shuguftha, Shelby Tyler, Yambem Olivia, Santra Santimukul
Department of Neurology, College of Medicine, University of Tennessee Health Science Center , 855 Monroe Avenue, Memphis, Tennessee 38163, United States.
Department of Chemistry, Kansas Polymer Research Center, Pittsburg State University , 1701 S. Broadway Street, Pittsburg, Kansas 66762, United States.
Mol Pharm. 2017 Mar 6;14(3):875-884. doi: 10.1021/acs.molpharmaceut.6b01076. Epub 2017 Jan 27.
K-RAS driven non-small-cell lung cancer (NSCLC) represents a major cause of death among smokers. Recently, nanotechnology has introduced novel avenues for the diagnosis and personalized treatment options for cancer. Herein, we report a novel, multifunctional nanoceria platform loaded with a unique combination of two therapeutic drugs, doxorubicin (Doxo) and Hsp90 inhibitor ganetespib (GT), for the diagnosis and effective treatment of NSCLC. We hypothesize that the use of ganetespib synergizes and accelerates the therapeutic efficacy of Doxo via ROS production, while minimizing the potential cardiotoxicity of doxorubicin drug. Polyacrylic acid (PAA)-coated cerium oxide nanoparticles (PNC) were fabricated for the targeted combination therapy of lung cancers. Using "click" chemistry, the surface carboxylic acid groups of nanoceria were decorated with folic acid to target folate-receptor-overexpressing NSCLC. As a result of combination therapy, results showed more than 80% of NSCLC death within 48 h of incubation. These synergistic therapeutic effects were assessed via enhanced ROS, cytotoxicity, apoptosis, and migration assays. Overall, these results indicated that the targeted codelivery of Doxo and GT using nanoceria may offer an alternative combination therapy option for the treatment of undruggable NSCLC.
K-RAS驱动的非小细胞肺癌(NSCLC)是吸烟者死亡的主要原因之一。最近,纳米技术为癌症的诊断和个性化治疗提供了新途径。在此,我们报告了一种新型多功能纳米氧化铈平台,该平台负载了两种治疗药物阿霉素(Doxo)和热休克蛋白90抑制剂ganetespib(GT)的独特组合,用于NSCLC的诊断和有效治疗。我们假设,使用ganetespib可通过产生ROS来协同并加速阿霉素的治疗效果,同时将阿霉素药物的潜在心脏毒性降至最低。制备了聚丙烯酸(PAA)包覆的氧化铈纳米颗粒(PNC)用于肺癌的靶向联合治疗。利用“点击”化学,用叶酸修饰纳米氧化铈的表面羧酸基团,以靶向叶酸受体过表达的NSCLC。联合治疗的结果显示,在孵育48小时内,超过80%的NSCLC细胞死亡。通过增强ROS、细胞毒性、凋亡和迁移试验评估了这些协同治疗效果。总体而言,这些结果表明,使用纳米氧化铈靶向共递送阿霉素和GT可能为治疗难治性NSCLC提供一种替代的联合治疗选择。