Use-inspired Biomaterials & Integrated Nano Delivery (U-BiND) Systems Laboratory Department of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, MI, 48201, USA; Department of Pharmaceutics and Pharmaceutical Technology, College of Pharmacy, Taif University, Taif, 25671, Saudi Arabia.
Use-inspired Biomaterials & Integrated Nano Delivery (U-BiND) Systems Laboratory Department of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, MI, 48201, USA.
Biomaterials. 2018 Nov;183:280-294. doi: 10.1016/j.biomaterials.2018.08.053. Epub 2018 Aug 30.
Drug resistance is one of the significant clinical burden in renal cell carcinoma (RCC). The development of drug resistance is attributed to many factors, including impairment of apoptosis, elevation of carbonic anhydrase IX (CA IX, a marker of tumor hypoxia), and infiltration of tumorigenic immune cells. To alleviate the drug resistance, we have used Sorafenib (Sor) in combination with tumor hypoxia directed nanoparticle (NP) loaded with a new class of apoptosis inducer, CFM 4.16 (C4.16), namely CA IX-C4.16. The NP is designed to selectively deliver the payload to the hypoxic tumor (core), provoke superior cell death in parental (WT) and Everolimus-resistant (Evr-res) RCC and selectively downmodulate tumorigenic M2-macrophage. Copper-free 'click' chemistry was utilized for conjugating SMA-TPGS with Acetazolamide (ATZ, a CA IX-specific targeting ligand). The NP was further tagged with a clinically approved NIR dye (S0456) for evaluating hypoxic tumor core penetration and organ distribution. Imaging of tumor spheroid treated with NIR dye-labeled CA IX-SMA-TPGS revealed remarkable tumor core penetration that was modulated by CA IX-mediated targeting in hypoxic-A498 RCC cells. The significant cell killing effect with synergistic combination index (CI) of CA IX-C4.16 and Sor treatment suggests efficient reversal of Evr-resistance in A498 cells. The CA IX directed nanoplatform in combination with Sor has shown multiple benefits in overcoming drug resistance through (i) inhibition of p-AKT, (ii) upregulation of tumoricidal M1 macrophages resulting in induction of caspase 3/7 mediated apoptosis of Evr-res A498 cells in macrophage-RCC co-culturing condition, (iii) significant in vitro and in vivo Evr-res A498 tumor growth inhibition as compared to individual therapy, and (iv) untraceable liver and kidney toxicity in mice. Near-infrared (NIR) imaging of CA IX-SMA-TPGS-S0456 in Evr-res A498 RCC model exhibited significant accumulation of CA IX-oligomer in tumor core with >3-fold higher tumor uptake as compared to control. In conclusion, this proof-of-concept study demonstrates versatile tumor hypoxia directed nanoplatform that can work in synergy with existing drugs for reversing drug-resistance in RCC accompanied with re-education of tumor-associated macrophages, that could be applied universally for several hypoxic tumors.
耐药性是肾细胞癌 (RCC) 的重大临床负担之一。耐药性的发展归因于许多因素,包括细胞凋亡受损、碳酸酐酶 IX(CA IX,肿瘤缺氧的标志物)升高以及肿瘤发生免疫细胞浸润。为了减轻耐药性,我们使用 Sorafenib(Sor)联合针对肿瘤缺氧的纳米颗粒(NP),NP 负载新型凋亡诱导剂 CFM 4.16(C4.16),即 CA IX-C4.16。NP 旨在选择性地将有效载荷递送至缺氧肿瘤(核心),在亲本(WT)和 Everolimus 耐药(Evr-res)RCC 中引发更好的细胞死亡,并选择性地下调肿瘤发生的 M2 巨噬细胞。铜自由“点击”化学用于将 SMA-TPGS 与 Acetazolamide(ATZ,CA IX 特异性靶向配体)偶联。NP 进一步标记有临床批准的近红外染料(S0456),用于评估缺氧肿瘤核心的穿透性和器官分布。用近红外染料标记的 CA IX-SMA-TPGS 处理的肿瘤球体成像显示,在缺氧 A498 RCC 细胞中,CA IX 介导的靶向作用调节了明显的肿瘤核心穿透性。CA IX-C4.16 和 Sor 联合治疗的协同组合指数(CI)的显著细胞杀伤作用表明,A498 细胞中的 Evr-res 耐药性得到有效逆转。与单独治疗相比,CA IX 导向的纳米平台与 Sor 的联合使用在克服耐药性方面具有多种优势,包括(i)抑制 p-AKT,(ii)上调肿瘤杀伤性 M1 巨噬细胞,从而诱导 caspase 3/7 介导的 Evr-res A498 细胞凋亡在巨噬细胞-RCC 共培养条件下,(iii)在体外和体内显著抑制 Evr-res A498 肿瘤生长,(iv)在小鼠中无肝肾功能毒性。Evr-res A498 RCC 模型中 CA IX-SMA-TPGS-S0456 的近红外(NIR)成像显示,与对照相比,肿瘤核心中 CA IX 寡聚物的积累显著增加了>3 倍。总之,这项概念验证研究表明,多功能肿瘤缺氧导向纳米平台可以与现有药物协同作用,逆转 RCC 的耐药性,并重新教育肿瘤相关巨噬细胞,可普遍应用于几种缺氧肿瘤。