Institute of Medical Science and Technology, National Sun Yat-sen University, 70 Lienhai Rd., Kaohsiung 80424, Taiwan.
Nanoscale. 2019 Apr 25;11(17):8102-8109. doi: 10.1039/c9nr01247h.
The proof-of-concept strategy in this study based on biodegradable and biocompatible self-assembling fluorescent virus-like particle/RNAi nanocomplexes (VLP/RNAi) produced in Escherichia coli (E. coli) followed by surface modification with a cell-penetrating peptide (CPP) and an apolipoprotein E peptide (ApoEP) (dP@VLP/RNAi), which can cross the blood-brain barrier (BBB) to inhibit the DNA repair mechanism and act synergistically with temozolomide (TMZ) for promoting clinical chemotherapy has achieved good therapeutic effects towards malignant brain tumors. The synergistic value of this study's design was verified in intracranial mouse models of glioblastomas (GBMs). Intravenous administration of this formulation enhanced the curative efficacy of TMZ by downregulating the hepatocyte growth factor receptor (c-MET) gene in GBM U87 cells. Furthermore, upon gene-chemotherapy, the methylated DNA in GBM U87 cells was significantly enhanced by inhibiting the DNA repair mechanism, leading to significant brain tumor suppression. The results of this study could be critical for the design of RNAi-based genetic therapeutics for promoting chemotherapy against brain tumors.
本研究采用基于可生物降解和生物相容的自组装荧光病毒样颗粒/RNAi 纳米复合物(VLP/RNAi)的概念验证策略,该复合物由大肠杆菌(E. coli)产生,然后用穿透肽(CPP)和载脂蛋白 E 肽(ApoEP)进行表面修饰(dP@VLP/RNAi),可穿透血脑屏障(BBB)抑制 DNA 修复机制,并与替莫唑胺(TMZ)协同作用,促进临床化疗,对恶性脑肿瘤取得了良好的治疗效果。该研究设计的协同价值在颅内胶质母细胞瘤(GBM)小鼠模型中得到了验证。该制剂的静脉给药通过下调 GBM U87 细胞中的肝细胞生长因子受体(c-MET)基因,增强了 TMZ 的治疗效果。此外,在基因化疗后,通过抑制 DNA 修复机制,显著增强了 GBM U87 细胞中的甲基化 DNA,从而显著抑制脑肿瘤。本研究的结果对于设计基于 RNAi 的基因治疗以促进针对脑肿瘤的化疗可能至关重要。