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克服神经母细胞瘤治疗中的生物学障碍:脂质体药物纳米载体的血管靶向方法。

Overcoming Biological Barriers in Neuroblastoma Therapy: The Vascular Targeting Approach with Liposomal Drug Nanocarriers.

机构信息

Laboratory of Experimental Therapies in Oncology, IRCCS Istituto Giannina Gaslini, 16147, Genoa, Italy.

Tumor Biology and Vascular Targeting Unit, IRCCS San Raffaele Scientific Institute, 16132, Milan, Italy.

出版信息

Small. 2019 Mar;15(10):e1804591. doi: 10.1002/smll.201804591. Epub 2019 Feb 1.

Abstract

Neuroblastoma is a rare pediatric cancer characterized by a wide clinical behavior and adverse outcome despite aggressive therapies. New approaches based on targeted drug delivery may improve efficacy and decrease toxicity of cancer therapy. Furthermore, nanotechnology offers additional potential developments for cancer imaging, diagnosis, and treatment. Following these lines, in the past years, innovative therapies based on the use of liposomes loaded with anticancer agents and functionalized with peptides capable of recognizing neuroblastoma cells and/or tumor-associated endothelial cells have been developed. Studies performed in experimental orthotopic models of human neuroblastoma have shown that targeted nanocarriers can be exploited for not only decreasing the systemic toxicity of the encapsulated anticancer drugs, but also increasing their tumor homing properties, enhancing tumor vascular permeability and perfusion (and, consequently, drug penetration), inducing tumor apoptosis, inhibiting angiogenesis, and reducing tumor glucose consumption. Furthermore, peptide-tagged liposomal formulations are proved to be more efficacious in inhibiting tumor growth and metastatic spreading of neuroblastoma than nontargeted liposomes. These findings, herein reviewed, pave the way for the design of novel targeted liposomal nanocarriers useful for multitargeting treatment of neuroblastoma.

摘要

神经母细胞瘤是一种罕见的儿科癌症,其临床行为广泛,尽管采用了积极的治疗方法,但预后仍较差。基于靶向药物递送的新方法可能会提高癌症治疗的疗效并降低毒性。此外,纳米技术为癌症成像、诊断和治疗提供了额外的潜在发展。基于这些思路,在过去几年中,已经开发出了基于使用载有抗癌药物的脂质体并通过能够识别神经母细胞瘤细胞和/或肿瘤相关内皮细胞的肽进行功能化的创新疗法。在人类神经母细胞瘤的实验性原位模型中进行的研究表明,靶向纳米载体不仅可以降低包裹的抗癌药物的全身毒性,还可以增加其肿瘤归巢特性,增强肿瘤血管通透性和灌注(因此,药物渗透),诱导肿瘤细胞凋亡,抑制血管生成,并减少肿瘤葡萄糖消耗。此外,与非靶向脂质体相比,肽标记的脂质体制剂在抑制神经母细胞瘤的肿瘤生长和转移扩散方面更有效。本文综述了这些发现,为设计新型靶向脂质体纳米载体用于神经母细胞瘤的多靶向治疗铺平了道路。

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