CAS Center for Excellence in Nanoscience, CAS Key Laboratory of Biomedical Effects of Nanomaterials and Nanosafety, National Center for Nanoscience and Technology, Beijing, 100190, P. R. China.
University of Chinese Academy of Sciences, Beijing, 100049, P. R. China.
Adv Mater. 2019 Nov;31(45):e1804814. doi: 10.1002/adma.201804814. Epub 2018 Nov 16.
Cancer remains one of the leading causes of death, which has continuously stimulated the development of numerous functional biomaterials with anticancer activities. Herein is reviewed one recent trend of biomaterials focusing on the advances in enzyme-instructed supramolecular self-assembly (EISA) with anticancer activity. EISA relies on enzymatic transformations to convert designed small-molecular precursors into corresponding amphiphilic residues that can form assemblies in living systems. EISA has shown some advantages in controlling cell fate from three aspects. 1) Based on the abnormal activity of specific enzymes, EISA can differentiate cancer cells from normal cells. In contrast to the classical ligand-receptor recognition, the targeting capability of EISA relies on dynamic control of the self-assembly process. 2) The interactions between EISA and cellular components directly disrupt cellular processes or pathways, resulting in cell death phenotypes. 3) EISA spatiotemporally controls the distribution of therapeutic agents, which boosts drug delivery efficiency. Therefore, with regard to the development of EISA, the aim is to provide a perspective on the future directions of research into EISA as anticancer theranostics.
癌症仍然是主要死因之一,这不断刺激了具有抗癌活性的众多功能生物材料的发展。本文综述了生物材料的一个最新趋势,重点介绍了具有抗癌活性的酶指导超分子自组装(EISA)的进展。EISA 依赖于酶转化将设计的小分子前体转化为相应的两亲性残基,这些残基可以在活系统中形成组装体。EISA 在控制细胞命运方面具有三个方面的优势。1)基于特定酶的异常活性,EISA 可以区分癌细胞和正常细胞。与经典的配体-受体识别不同,EISA 的靶向能力依赖于自组装过程的动态控制。2)EISA 与细胞成分之间的相互作用直接破坏细胞过程或途径,导致细胞死亡表型。3)EISA 时空控制治疗剂的分布,从而提高药物输送效率。因此,就 EISA 的发展而言,目的是提供一个关于 EISA 作为癌症治疗策略研究未来方向的视角。