Zhang Qian, Du Yang, Jing Lijia, Liang Xiaolong, Li Yaqian, Li Xiaofeng, Dai Zhifei, Tian Jie
J Biomed Nanotechnol. 2016 Mar;12(3):491-502. doi: 10.1166/jbn.2016.2022.
Endostar, a novel recombinant human endostatin, has been proven to inhibit tumor angiogenesis and is utilized as an anticancer drug. While free drugs can display limited efficacy, nanoscaled anticancer drugs have been fabricated and proven to possess superior therapeutic effects. Poly(lactic acid) (PLA) is a FDA-approved biomaterial displaying excellent biocompatibility and low toxicity. In this study, Endostar-loaded PLA nanoparticles (EPNPs) were first prepared, and a near-infrared (NIR) dye, IRDye 800CW, was conjugated to the surface for detecting nanoparticle biodistribution through fluorescence molecular imaging (FMI) using an orthotopic breast tumor mouse model. The antitumor efficacy of EPNPs was examined using bioluminescence imaging (BLI) and immunohistology. To further improve the antitumor effects, we combined EPNPs with zoledronic acid monohydrate (ZA), which is known to decrease the tumor-associated macrophages (TAM) and inhibit tumor progression. We found that EPNPs decreased human umbilical vein endothelial cell (HUVEC) viability by inhibiting tumor growth gene expression more significantly than free Endostar in vitro. In vivo, EPNPs displayed better tumor growth inhibitory effects compared with free Endostar, and the combination of EPNPs with ZA exhibited more significant antitumor effects. As confirmed by CD31 and CD11b immunohistochemistry, the combination of EPNPs and ZA showed synergistic effects in reducing tumor angiogenesis and TAM accumulation in tumor regions. Taken together, this study presents a novel and effective form of nanoscaled Endostar for the treatment of breast cancer that displays synergistic antitumor effects in combination with ZA.
恩度是一种新型重组人内皮抑素,已被证明可抑制肿瘤血管生成,并被用作抗癌药物。虽然游离药物的疗效有限,但已制备出纳米级抗癌药物并证明其具有卓越的治疗效果。聚乳酸(PLA)是一种经美国食品药品监督管理局(FDA)批准的生物材料,具有出色的生物相容性和低毒性。在本研究中,首先制备了负载恩度的聚乳酸纳米颗粒(EPNPs),并将一种近红外(NIR)染料IRDye 800CW偶联到其表面,通过荧光分子成像(FMI),利用原位乳腺癌小鼠模型检测纳米颗粒的生物分布。使用生物发光成像(BLI)和免疫组织学方法检测了EPNPs的抗肿瘤疗效。为了进一步提高抗肿瘤效果,我们将EPNPs与一水合唑来膦酸(ZA)联合使用,已知ZA可减少肿瘤相关巨噬细胞(TAM)并抑制肿瘤进展。我们发现,在体外,EPNPs通过更显著地抑制肿瘤生长基因表达来降低人脐静脉内皮细胞(HUVEC)的活力,比游离恩度更有效。在体内,与游离恩度相比,EPNPs显示出更好的肿瘤生长抑制作用,并且EPNPs与ZA联合使用表现出更显著的抗肿瘤效果。经CD31和CD11b免疫组织化学证实,EPNPs与ZA联合使用在减少肿瘤血管生成和肿瘤区域TAM聚集方面显示出协同作用。综上所述,本研究提出了一种新型且有效的纳米级恩度形式用于治疗乳腺癌,其与ZA联合使用时表现出协同抗肿瘤作用。