Endothelial Cell Adhesion Molecules- (un)Attainable Targets for Nanomedicines

IF 2.7 Q3 ENGINEERING, BIOMEDICAL
N. Milosevic, M. Rütter, A. David
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引用次数: 4

Abstract

Endothelial cell adhesion molecules have long been proposed as promising targets in many pathologies. Despite promising preclinical data, several efforts to develop small molecule inhibitors or monoclonal antibodies (mAbs) against cell adhesion molecules (CAMs) ended in clinical-stage failure. In parallel, many well-validated approaches for targeting CAMs with nanomedicine (NM) were reported over the years. A wide range of potential applications has been demonstrated in various preclinical studies, from drug delivery to the tumor vasculature, imaging of the inflamed endothelium, or blocking immune cells infiltration. However, no NM drug candidate emerged further into clinical development. In this review, we will summarize the most advanced examples of CAM-targeted NMs and juxtapose them with known traditional drugs against CAMs, in an attempt to identify important translational hurdles. Most importantly, we will summarize the proposed strategies to enhance endothelial CAM targeting by NMs, in an attempt to offer a catalog of tools for further development.
内皮细胞粘附分子-纳米药物(无法)达到的目标
内皮细胞粘附分子长期以来被认为是许多病理的有希望的靶点。尽管有很好的临床前数据,但开发抗细胞粘附分子(CAMs)的小分子抑制剂或单克隆抗体(mab)的一些努力以临床阶段失败告终。与此同时,近年来也报道了许多经过验证的纳米药物靶向cam的方法。广泛的潜在应用已经在各种临床前研究中得到证明,从药物输送到肿瘤血管,炎症内皮的成像,或阻断免疫细胞浸润。然而,没有任何NM候选药物进一步进入临床开发。在这篇综述中,我们将总结针对cam的最先进的NMs的例子,并将它们与已知的针对cam的传统药物并列,试图找出重要的转化障碍。最重要的是,我们将总结提出的策略,以增强内皮CAM靶向NMs,试图提供一个工具目录,以进一步发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.70
自引率
0.00%
发文量
0
审稿时长
13 weeks
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