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适体:用于癌症检测的多功能分子识别探针。

Aptamers: versatile molecular recognition probes for cancer detection.

作者信息

Sun Hongguang, Tan Weihong, Zu Youli

机构信息

Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX 77030, USA.

Department of Chemistry and Physiology and Functional Genomics, Center for Research at the Bio/Nano Interface, Shands Cancer Center, UF Genetics Institute, University of Florida, Gainesville, Florida 32611-7200, USA.

出版信息

Analyst. 2016 Jan 21;141(2):403-15. doi: 10.1039/c5an01995h.

Abstract

In the past two decades, aptamers have emerged as a novel class of molecular recognition probes comprising uniquely-folded short RNA or single-stranded DNA oligonucleotides that bind to their cognate targets with high specificity and affinity. Aptamers, often referred to as "chemical antibodies", possess several highly desirable features for clinical use. They can be chemically synthesized and are easily conjugated to a wide range of reporters for different applications, and are able to rapidly penetrate tissues. These advantages significantly enhance their clinical applicability, and render them excellent alternatives to antibody-based probes in cancer diagnostics and therapeutics. Aptamer probes based on fluorescence, colorimetry, magnetism, electrochemistry, and in conjunction with nanomaterials (e.g., nanoparticles, quantum dots, single-walled carbon nanotubes, and magnetic nanoparticles) have provided novel ultrasensitive cancer diagnostic strategies and assays. Furthermore, promising aptamer targeted-multimodal tumor imaging probes have been recently developed in conjunction with fluorescence, positron emission tomography (PET), single-photon emission computed tomography (SPECT), and magnetic resonance imaging (MRI). The capabilities of the aptamer-based platforms described herein underscore the great potential they hold for the future of cancer detection. In this review, we highlight the most prominent recent developments in this rapidly advancing field.

摘要

在过去二十年中,适体已成为一类新型分子识别探针,由独特折叠的短RNA或单链DNA寡核苷酸组成,它们以高特异性和亲和力与其同源靶标结合。适体常被称为“化学抗体”,具有临床应用中几个非常理想的特性。它们可以化学合成,易于与用于不同应用的多种报告分子偶联,并且能够迅速穿透组织。这些优势显著提高了它们的临床适用性,使其成为癌症诊断和治疗中基于抗体的探针的极佳替代品。基于荧光、比色法、磁性、电化学以及与纳米材料(如纳米颗粒、量子点、单壁碳纳米管和磁性纳米颗粒)结合的适体探针提供了新型超灵敏癌症诊断策略和检测方法。此外,最近还开发了结合荧光、正电子发射断层扫描(PET)、单光子发射计算机断层扫描(SPECT)和磁共振成像(MRI)的有前景的适体靶向多模态肿瘤成像探针。本文所述基于适体的平台的能力突出了它们在癌症检测未来发展中所具有的巨大潜力。在本综述中,我们重点介绍了这一快速发展领域中最突出的最新进展。

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