肿瘤成像的目标选择:癌症相关膜蛋白的概述

M. C. Boonstra, S. D. de Geus, H. A. Prevoo, L. Hawinkels, C. J. van de Velde, P. Kuppen, A. Vahrmeijer, C. Sier
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引用次数: 80

摘要

肿瘤靶向治疗是一项蓬勃发展的业务:2012年,全球治疗性单克隆抗体市场规模超过780亿美元,并呈指数级增长。肿瘤可以用广泛的单克隆抗体、配体蛋白、多肽、rna和小分子靶向。除了靶向治疗外,其中一些化合物还可以在手术前或手术中,在与放射性核素和/或近红外荧光染料结合后用于肿瘤可视化。这些肿瘤靶向化合物中的大多数是针对细胞膜结合蛋白的。存在各种类型的可靶向膜结合蛋白,如锚定蛋白、受体、酶和转运蛋白。这些蛋白质的功能和生物学特性决定了它们在细胞膜上的位置和分布,使它们更容易或更不容易接近,因此,了解这些特性非常重要。在这篇综述中,我们评估了癌症相关膜蛋白的特征,并讨论了它们在癌症靶向方面的总体可用性,特别是在成像方面的应用。
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Selecting Targets for Tumor Imaging: An Overview of Cancer-Associated Membrane Proteins
Tumor targeting is a booming business: The global therapeutic monoclonal antibody market accounted for more than $78 billion in 2012 and is expanding exponentially. Tumors can be targeted with an extensive arsenal of monoclonal antibodies, ligand proteins, peptides, RNAs, and small molecules. In addition to therapeutic targeting, some of these compounds can also be applied for tumor visualization before or during surgery, after conjugation with radionuclides and/or near-infrared fluorescent dyes. The majority of these tumor-targeting compounds are directed against cell membrane-bound proteins. Various categories of targetable membrane-bound proteins, such as anchoring proteins, receptors, enzymes, and transporter proteins, exist. The functions and biological characteristics of these proteins determine their location and distribution on the cell membrane, making them more, or less, accessible, and therefore, it is important to understand these features. In this review, we evaluate the characteristics of cancer-associated membrane proteins and discuss their overall usability for cancer targeting, especially focusing on imaging applications.
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