Jiangsu Key Laboratory of Druggability of Biopharmaceuticals, State Key Laboratory of Natural Medicines, School of Life Science and Technology, China Pharmaceutical University, Nanjing 210009, China.
Jiangsu Key Laboratory of Druggability of Biopharmaceuticals, State Key Laboratory of Natural Medicines, School of Life Science and Technology, China Pharmaceutical University, Nanjing 210009, China.
J Control Release. 2022 Jun;346:250-259. doi: 10.1016/j.jconrel.2022.04.022. Epub 2022 Apr 27.
Multidrug resistance (MDR) to chemotherapeutic drugs and targeted drug delivery are recurring issues in clinical cancer treatment. Here, a multifunctional fusion protein-DNA conjugate was designed as a co-delivery vehicle for anticancer peptides and chemotherapeutic drugs to combat both drug-resistant and drug-sensitive tumor cells. The fusion protein was constructed by fusing a PsTag polypeptide, a matrix metalloproteinase 2 (MMP2)-degradable domain, and the mitochondria-targeted pro-apoptotic peptide KLAKLAKKLAKLAK. Doxorubicin was efficiently loaded into the fusion protein pre-conjugated dendrimer-like DNA nanostructure. With the incorporation of enhanced stability, tumor targeting, and controlled-release elements, the tailored nanostructure can selectively enter tumor cells and synergistically exert antitumor activity with no significant adverse effects. Thus, these protein-conjugated DNA nanocarriers could be a potential co-delivery system for protein/peptide and chemotherapeutic drugs delivery in synergistic cancer therapy.
多药耐药(MDR)对化疗药物和靶向药物递送是临床癌症治疗中反复出现的问题。在这里,设计了一种多功能融合蛋白-DNA 缀合物作为抗癌肽和化疗药物的共递药载体,以对抗耐药和敏感肿瘤细胞。融合蛋白通过融合 PsTag 多肽、基质金属蛋白酶 2(MMP2)可降解结构域和线粒体靶向促凋亡肽 KLAKLAKKLAKLAK 构建而成。阿霉素被高效地载入融合蛋白预缀合的树状大分子样 DNA 纳米结构中。通过加入增强的稳定性、肿瘤靶向性和控制释放元件,定制的纳米结构可以选择性进入肿瘤细胞,并与无明显不良反应的化疗药物协同发挥抗肿瘤活性。因此,这些蛋白偶联 DNA 纳米载体可能成为协同癌症治疗中蛋白/肽和化疗药物递释的潜在共递药系统。