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动态对比增强磁共振成像评估靶向多功能ECO/siRNA纳米颗粒沉默HIF-1α的抗血管生成作用

Dynamic Contrast Enhanced MRI Assessing the Antiangiogenic Effect of Silencing HIF-1α with Targeted Multifunctional ECO/siRNA Nanoparticles.

作者信息

Malamas Anthony S, Jin Erlei, Gujrati Maneesh, Lu Zheng-Rong

机构信息

Case Center for Biomolecular Engineering, Department of Biomedical Engineering, Case Western Reserve University , Cleveland, Ohio 44106, United States.

出版信息

Mol Pharm. 2016 Jul 5;13(7):2497-506. doi: 10.1021/acs.molpharmaceut.6b00227. Epub 2016 Jun 15.

Abstract

Stabilization of hypoxia inducible factor 1α (HIF-1α), a biomarker of hypoxia, in hypoxic tumors mediates a variety of downstream genes promoting tumor angiogenesis and cancer cell survival as well as invasion, and compromising therapeutic outcome. In this study, dynamic contrast enhanced MRI (DCE-MRI) with a biodegradable macromolecular MRI contrast agent was used to noninvasively assess the antiangiogenic effect of RGD-targeted multifunctional lipid ECO/siHIF-1α nanoparticles in a mouse HT29 colon cancer model. The RGD-targeted ECO/siHIF-1α nanoparticles resulted in over 50% reduction in tumor size after intravenous injection at a dose of 2.0 mg of siRNA/kg every 3 days for 3 weeks compared to a saline control. DCE-MRI revealed significant decline in vascularity and over a 70% reduction in the tumor blood flow, permeability-surface area product, and plasma volume fraction vascular parameters in the tumor treated with the targeted ECO/siHIF-1α nanoparticles. The treatment with targeted ECO/siRNA nanoparticles resulted in significant silencing of HIF-1α expression at the protein level, which also significantly suppressed the expression of VEGF, Glut-1, HKII, PDK-1, LDHA, and CAIX, which are all important players in tumor angiogenesis, glycolytic metabolism, and pH regulation. By possessing the ability to elicit a multifaceted effect on tumor biology, silencing HIF-1α with RGD-targeted ECO/siHIF-1α nanoparticles has great promise as a single therapy or in combination with traditional chemotherapy or radiation strategies to improve cancer treatment.

摘要

缺氧诱导因子1α(HIF-1α)是缺氧的生物标志物,在缺氧肿瘤中的稳定介导了多种下游基因,促进肿瘤血管生成、癌细胞存活以及侵袭,并损害治疗效果。在本研究中,使用可生物降解的大分子磁共振成像(MRI)造影剂的动态对比增强MRI(DCE-MRI)来无创评估RGD靶向的多功能脂质ECO/siHIF-1α纳米颗粒在小鼠HT29结肠癌模型中的抗血管生成作用。与生理盐水对照组相比,RGD靶向的ECO/siHIF-1α纳米颗粒以每3天2.0毫克siRNA/千克的剂量静脉注射3周后,肿瘤大小减少了50%以上。DCE-MRI显示,在用靶向ECO/siHIF-1α纳米颗粒治疗的肿瘤中,血管生成显著下降,肿瘤血流、通透表面积乘积和血浆体积分数血管参数减少了70%以上。用靶向ECO/siRNA纳米颗粒治疗导致HIF-1α蛋白水平的表达显著沉默,这也显著抑制了VEGF、Glut-1、HKII、PDK-1、LDHA和CAIX的表达,这些都是肿瘤血管生成、糖酵解代谢和pH调节中的重要参与者。通过对肿瘤生物学产生多方面的影响,用RGD靶向的ECO/siHIF-1α纳米颗粒沉默HIF-1α作为单一疗法或与传统化疗或放疗策略联合使用,在改善癌症治疗方面具有巨大潜力。

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