首页> 外文期刊>Biomaterials >LNA aptamer based multi-modal, Fe3O4-saturated lactoferrin (Fe3O4-bLf) nanocarriers for triple positive (EpCAM, CD133, CD44) colon tumor targeting and NIR, MRI and CT imaging
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LNA aptamer based multi-modal, Fe3O4-saturated lactoferrin (Fe3O4-bLf) nanocarriers for triple positive (EpCAM, CD133, CD44) colon tumor targeting and NIR, MRI and CT imaging

机译:基于LNA适体的多模式,Fe3O4饱和的乳铁蛋白(Fe3O4-bLf)纳米载体,可用于靶向三重阳性(EpCAM,CD133,CD44)结肠肿瘤以及NIR,MRI和CT成像

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This is the first ever attempt to combine anti-cancer therapeutic effects of emerging anticancer biodrug bovine lactoferrin (bLf), and multimodal imaging efficacy of Fe3O4 nanoparticles (NPs) together, as a saturated Fe3O4-bLf. For cancer stem cell specific uptake of nanocapsulesanocarriers (NCs), Fe3O4-bLf was encapsulated in alginate enclosed chitosan coated calcium phosphate (AEC-CP) NCs targeted (Tar) with locked nucleic acid (LNA) modified aptamers against epithelial cell adhesion molecule (EpCAM) and nucleolin markers. The nanoformulation was fed orally to mice injected with triple positive (EpCAM, CD133, CD44) sorted colon cancer stem cells in the xenograft cancer stem cell mice model. The complete regression of tumor was observed in 70% of mice fed on non-targeted (NT) NCs, with 30% mice showing tumor recurrence after 30 days, while only 10% mice fed with Tar NCs showed tumor recurrence indicating a significantly higher survival rate. From tumor tissue analyses of 35 apoptotic markers, 55 angiogenesis markers, 40 cytokines, 15 stem cell markers and gene expression studies of important signaling molecules, it was revealed that the anti-cancer mechanism of Fe3O4-bLf was intervened through TRAIL, Fas, Fas-associated protein with death domain (FADD) mediated phosphorylation of p53, to induce activation of second mitochondria-derived activator of caspases (SMAC)/DIABLO (inhibiting survivin) and mitochondrial depolarization leading to release of cytochrome C. Induction of apoptosis was observed by inhibition of the Akt pathway and activation of cytokines released from monocytes/macrophages and dendritic cells (interleukin (IL) 27, keratinocyte chemoattractant (KC)). On the other hand, the recurrence of tumor in AEC-CP-Fe3O4-bLf NCs fed mice mainly occurred due to activation of alternative pathways such as mitogen-activated protein kinases (MAPK)/extracellular signal-regulated kinases (ERIC) and Wnt signaling leading to an increase in expression of survivin, survivin splice variant (survivin 2B) and other anti-apoptotic proteins Bad, Bcl-2 and XIAP. Apart from the promising anti-cancer efficacy and the exceptional tumor targeting ability observed by multimodal imaging using near-infrared (NIR) imaging, magnetic resonance imaging (MRI) and computerized tomographic (CT) techniques, these NCs also maintained the immunomodulatory benefits of bLf as they were able to increase the RBC, hemoglobin, iron calcium and zinc levels in mice. (C) 2015 Elsevier Ltd. All rights reserved.
机译:这是有史以来第一次尝试将新兴的抗癌生物药物牛乳铁蛋白(bLf)的抗癌治疗效果与Fe3O4纳米颗粒(NPs)的多峰成像功效结合在一起,作为饱和的Fe3O4-bLf。对于癌症干细胞对纳米胶囊/纳米载体(NCs)的特异性摄取,将Fe3O4-bLf封装在藻酸盐封闭的壳聚糖包被的磷酸钙(AEC-CP)NCs中,靶向的(Tar)具有锁定核酸(LNA)修饰的适体,抵抗上皮细胞粘附分子(EpCAM)和核仁标记物。在异种移植癌干细胞小鼠模型中,将纳米制剂口服喂入注射了三重阳性(EpCAM,CD133,CD44)分选的结肠癌干细胞的小鼠。在非靶向(NT)NCs喂养的小鼠中,有70%观察到肿瘤完全消退,其中30%的小鼠在30天后显示出肿瘤复发,而只有10%的Tar Tar NCs喂养的小鼠显示出肿瘤复发,表明存活率显着提高率。通过对35种凋亡标志物,55种血管生成标志物,40种细胞因子,15种干细胞标志物的肿瘤组织分析以及重要信号分子的基因表达研究,揭示了Fe3O4-bLf的抗癌机制是通过TRAIL,Fas,Fas干预的。与死亡域相关的蛋白质(FADD)介导的p53磷酸化,诱导第二个线粒体衍生的胱天蛋白酶(SMAC)/ DIABLO激活剂(抑制survivin)的活化和线粒体去极化导致细胞色素C的释放。抑制Akt途径并激活单核细胞/巨噬细胞和树突状细胞释放的细胞因子(白介素(IL)27,角质形成细胞趋化因子(KC))。另一方面,AEC-CP-Fe3O4-bLf NCs喂养的小鼠中肿瘤的复发主要是由于激活了其他途径,如促分裂原激活的蛋白激酶(MAPK)/细胞外信号调节激酶(ERIC)和Wnt信号传导导致survivin,survivin剪接变体(survivin 2B)和其他抗凋亡蛋白Bad,Bcl-2和XIAP的表达增加。除了通过使用近红外(NIR)成像,磁共振成像(MRI)和计算机断层扫描(CT)技术的多模式成像观察到的有希望的抗癌功效和卓越的肿瘤靶向能力外,这些NC还保持了bLf的免疫调节优势因为它们能够增加小鼠的RBC,血红蛋白,铁钙和锌水平。 (C)2015 Elsevier Ltd.保留所有权利。

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