Fels Institute for Cancer Research & Molecular Biology, Lewis Katz School of Medicine, Temple University, Philadelphia, Pennsylvania, 19140, USA.
School of Pharmacy, Temple University, Philadelphia, Pennsylvania, 19140, USA.
AAPS PharmSciTech. 2021 Mar 8;22(3):93. doi: 10.1208/s12249-021-01919-w.
Heterogeneity in tumor expression as well as expression in normal tissues of various targets limit the usefulness of current ligand-based active targeting approaches. Incorporation of synthetic receptors, which can be recognized by delivery systems engineered to present specific functional groups on the surface, is a novel approach to improve tumor targeting. Alternatively, introduction of synthetic functionalities on cellular carriers can also enhance tumor targeting. We review various strategies that have been utilized for the introduction of synthetic targets in tumor tissues. The introduction of synthetic functional groups in the tumor through improved strategies is anticipated to result in improved target specificity and reduced heterogeneity in target expression.
肿瘤表达的异质性以及各种靶标在正常组织中的表达限制了当前基于配体的主动靶向方法的实用性。将可以被设计为在表面呈现特定功能基团的输送系统识别的合成受体的结合是一种提高肿瘤靶向性的新方法。另外,在细胞载体上引入合成功能也可以增强肿瘤靶向性。我们综述了用于在肿瘤组织中引入合成靶标的各种策略。通过改进的策略在肿瘤中引入合成功能基团,预期会导致提高靶标特异性和降低靶标表达的异质性。