Chen Ke, Liu Bo, Yu Bo, Zhong Wen, Lu Yi, Zhang Jiani, Liao Jie, Liu Jun, Pu Ying, Qiu Liping, Zhang Liqin, Liu Huixia, Tan Weihong
Xiangya Hospital, Central South University, Changsha, China.
Molecular Science and Biomedicine Laboratory, Hunan University, Changsha, China.
Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2017 May;9(3). doi: 10.1002/wnan.1438. Epub 2016 Oct 31.
A key goal of modern medicine is target-specific therapeutic intervention. However, most drugs lack selectivity, resulting in 'off-target' side effects. To address the requirements of 'targeted therapy,' aptamers, which are artificial oligonucleotides, have been used as novel targeting ligands to construct aptamer drug conjugates (ApDC) that can specifically bind to a broad spectrum of targets, including diseased cells. Accordingly, the application of aptamers in targeted drug delivery has attracted broad interest due to their impressive selectivity and affinity, low immunogenicity, easy synthesis with high reproducibility, facile modification, and relatively rapid tissue penetration with no toxicity. Functionally, aptamers themselves can be used as macromolecular drugs, and they are also commonly used in biomarker discovery and targeted drug delivery. In this review, we will highlight the most recent advances in the development of aptamers and aptamer conjugates, and discuss their potential in targeted therapy. WIREs Nanomed Nanobiotechnol 2017, 9:e1438. doi: 10.1002/wnan.1438 For further resources related to this article, please visit the WIREs website.
现代医学的一个关键目标是进行靶向特异性治疗干预。然而,大多数药物缺乏选择性,会产生“脱靶”副作用。为满足“靶向治疗”的要求,适配体(一种人工合成的寡核苷酸)已被用作新型靶向配体,用于构建可特异性结合包括病变细胞在内的广泛靶点的适配体药物偶联物(ApDC)。因此,适配体因其出色的选择性和亲和力、低免疫原性、易于合成且可重复性高、易于修饰以及相对快速的组织穿透性且无毒性,在靶向药物递送中的应用引起了广泛关注。从功能上讲,适配体本身可作为大分子药物,也常用于生物标志物发现和靶向药物递送。在本综述中,我们将重点介绍适配体及适配体偶联物开发的最新进展,并讨论它们在靶向治疗中的潜力。《WIREs纳米医学与纳米生物技术》2017年,9:e1438。doi:10.1002/wnan.1438 有关本文的更多资源,请访问WIREs网站。