Department of Radiology, Stanford University, Palo Alto, CA, USA.
Nanomedicine (Lond). 2018 May;13(9):1051-1066. doi: 10.2217/nnm-2017-0328. Epub 2018 May 23.
Triple-negative breast cancer (TNBC) is an aggressive breast cancer subtype. Since no targeted therapy is available, gene-directed enzyme prodrug therapy (GDEPT) could be an attractive strategy for treating TNBC.
MATERIALS & METHODS: Polyethylene glycol (PEG)ylated-poly(lactic-co-glycolic acid)/polyethyleneimine nanoparticles (PLGA/PEI NPs) were synthesized and complexed with TK-NTR fusion gene. Ultrasound (US) and microbubble (MB) mediated sonoporation was used for efficient delivery of the TK-NTR-DNA-NP complex to TNBC tumor in vivo for cancer therapy. Therapeutic effect was evaluated by treating TNBC cells in vitro and tumor xenograft in vivo by using prodrugs ganciclovir (GCV) and CB1954.
TNBC cells treated with GCV/CB1954 prodrugs after transfection of TK-NTR-DNA by PEGylated-PLGA/PEI NP resulted in high apoptotic-index. US-MB image-guided delivery of TK-NTR-DNA-NP complex displayed significant expression level of TK-NTR protein and showed tumor reduction when treated with GCV/CB1954 prodrugs in TNBC xenograft in vivo.
US-MB image-guided delivery of TK-NTR gene by PEGylated-PLGA/PEI NPs could be a potential prodrug therapy for TNBC in the clinic.
三阴性乳腺癌(TNBC)是一种侵袭性乳腺癌亚型。由于目前尚无靶向治疗方法,基因定向酶前体药物治疗(GDEPT)可能是治疗 TNBC 的一种有吸引力的策略。
合成聚乙二醇(PEG)化聚(乳酸-共-乙醇酸)/聚乙烯亚胺纳米颗粒(PLGA/PEI NPs),并与 TK-NTR 融合基因复合。超声(US)和微泡(MB)介导的声孔法用于将 TK-NTR-DNA-NP 复合物高效递送至体内 TNBC 肿瘤,用于癌症治疗。通过用前体药物更昔洛韦(GCV)和 CB1954 体外处理 TNBC 细胞和体内肿瘤异种移植,评估治疗效果。
用 PEGylated-PLGA/PEI NP 转染 TK-NTR-DNA 后,用 GCV/CB1954 前体药物处理的 TNBC 细胞导致高凋亡指数。US-MB 图像引导的 TK-NTR-DNA-NP 复合物的递送显示出 TK-NTR 蛋白的显著表达水平,并在体内 TNBC 异种移植中用 GCV/CB1954 前体药物处理时显示出肿瘤缩小。
PEGylated-PLGA/PEI NPs 介导的 US-MB 图像引导的 TK-NTR 基因传递可能是 TNBC 临床前药物治疗的一种有潜力的方法。