Brinkman Ashley M, Chen Guojun, Wang Yidan, Hedman Curtis J, Sherer Nathan M, Havighurst Thomas C, Gong Shaoqin, Xu Wei
McArdle Laboratory for Cancer Research, University of Wisconsin - Madison, Madison, WI, USA.
Molecular and Environmental Toxicology Center, University of Wisconsin - Madison, Madison, WI, USA.
Biomaterials. 2016 Sep;101:20-31. doi: 10.1016/j.biomaterials.2016.05.041. Epub 2016 May 27.
Triple negative breast cancer (TNBC) is an aggressive subtype of breast cancer for which there is no available targeted therapy. TNBC cases contribute disproportionately to breast cancer-related mortality, thus the need for novel and effective therapeutic methods is urgent. We have previously shown that a National Cancer Institute (NCI) investigational drug aminoflavone (AF) exhibits strong growth inhibitory effects in TNBC cells. However, in vivo pulmonary toxicity resulted in withdrawal or termination of several human clinical trials for AF. Herein we report the in vivo efficacy of a nanoformulation of AF that enhances the therapeutic index of AF in TNBC. We engineered a unique unimolecular micelle nanoparticle (NP) loaded with AF and conjugated with GE11, a 12 amino acid peptide targeting epidermal growth factor receptor (EGFR), since EGFR amplification is frequently observed in TNBC tumors. These unimolecular micelles possessed excellent stability and preferentially released drug payload at endosomal pH levels rather than blood pH levels. Use of the GE11 targeting peptide resulted in enhanced cellular uptake and strong growth inhibitory effects in TNBC cells. Further, AF-loaded, GE11-conjugated (targeted) unimolecular micelle NPs significantly inhibit orthotopic TNBC tumor growth in a xenograft model, compared to treatment with AF-loaded, GE11-lacking (non-targeted) unimolecular micelle NPs or free AF. Interestingly, the animals treated with AF-loaded, targeted NPs had the highest plasma and tumor level of AF among different treatment groups yet exhibited no increase in plasma aspartate aminotransferase (AST) activity level or observable tissue damage at the time of sacrifice. Together, these results highlight AF-loaded, EGFR-targeted unimolecular micelle NPs as an effective therapeutic option for EGFR-overexpressing TNBC.
三阴性乳腺癌(TNBC)是一种侵袭性乳腺癌亚型,目前尚无可用的靶向治疗方法。TNBC病例在乳腺癌相关死亡率中所占比例过高,因此迫切需要新的有效治疗方法。我们之前已经表明,美国国立癌症研究所(NCI)的一种研究性药物氨基黄酮(AF)在TNBC细胞中表现出强大的生长抑制作用。然而,体内肺部毒性导致AF的几项人体临床试验被撤回或终止。在此,我们报告了AF纳米制剂的体内疗效,该纳米制剂提高了AF在TNBC中的治疗指数。我们设计了一种独特的单分子胶束纳米颗粒(NP),其负载AF并与GE11偶联,GE11是一种靶向表皮生长因子受体(EGFR)的12氨基酸肽,因为在TNBC肿瘤中经常观察到EGFR扩增。这些单分子胶束具有出色的稳定性,并且在内体pH水平而非血液pH水平下优先释放药物。GE11靶向肽的使用导致TNBC细胞的细胞摄取增强和强大的生长抑制作用。此外,与用负载AF、缺乏GE11(非靶向)的单分子胶束NP或游离AF治疗相比,负载AF、偶联GE11(靶向)的单分子胶束NP在异种移植模型中显著抑制原位TNBC肿瘤生长。有趣的是,在不同治疗组中,用负载AF的靶向NP治疗的动物血浆和肿瘤中的AF水平最高,但在处死时血浆天冬氨酸转氨酶(AST)活性水平没有增加,也没有观察到组织损伤。总之,这些结果突出了负载AF、靶向EGFR的单分子胶束NP作为EGFR过表达TNBC的一种有效治疗选择。