Key Laboratory for Advanced Materials, Feringa Nobel Prize Scientist Joint Research Center, Joint International Laboratory for Precision Chemistry, Frontiers Science Center for Materiobiology & Dynamic Chemistry, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai, 200237, P. R. China.
Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
Angew Chem Int Ed Engl. 2022 Dec 5;61(49):e202210935. doi: 10.1002/anie.202210935. Epub 2022 Nov 9.
Despite the promise of combination cancer therapy, it remains challenging to develop targeted strategies that are nontoxic to normal cells. Here we report a combination therapeutic strategy based on engineered DNAzyme molecular machines that can promote cancer apoptosis via dynamic inter- and intracellular regulation. To achieve external regulation of T-cell/cancer cell interactions, we designed a DNAzyme-based molecular machine with an aptamer and an i-motif, as the MUC-1-selective aptamer allows the specific recognition of cancer cells. The i-motif is folded under the tumor acidic microenvironment, shortening the intercellular distance. As a result, T-cells are released by metal ion activated DNAzyme cleavage. To achieve internal regulation of mitochondria, we delivered another DNAzyme-based molecular machine with mitochondria-targeted peptides into cancer cells to induce mitochondria aggregation. Our strategy achieved an enhanced killing effect in zinc deficient cancer cells.
尽管联合癌症疗法前景广阔,但开发对正常细胞无毒的靶向策略仍然具有挑战性。在这里,我们报告了一种基于工程 DNAzyme 分子机器的组合治疗策略,该策略可以通过动态的细胞内外调节促进癌症细胞凋亡。为了实现 T 细胞/癌细胞相互作用的外部调节,我们设计了一种基于 DNAzyme 的分子机器,该机器带有适体和 i-motif,因为 MUC-1 选择性适体允许对癌细胞进行特异性识别。i-motif 在肿瘤酸性微环境下折叠,缩短了细胞间距离。结果,T 细胞被金属离子激活的 DNA 酶切割释放。为了实现线粒体的内部调节,我们将另一种带有靶向线粒体肽的基于 DNAzyme 的分子机器递送到癌细胞中,以诱导线粒体聚集。我们的策略在缺锌的癌细胞中实现了增强的杀伤效果。
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