Department of Radiology, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai Jiao Tong University School of Medicine, 600 Yi Shan Road, Shanghai 200233, China.
School of Chemistry and Chemical Engineering, Frontiers Science Center for Transformative Molecules, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, China.
Sci Adv. 2022 Apr 22;8(16):eabn2941. doi: 10.1126/sciadv.abn2941. Epub 2022 Apr 20.
Packaging multiple drugs into a nanocarrier with rational design to achieve synergistic cancer therapy remains a challenge due to the intrinsically varied pharmacodynamics of therapeutic agents. Especially difficult is combining small-molecule drugs and macromolecular biologics. Here, we successfully graft pheophorbide A (PPA) photosensitizers on DNA backbone at predesigned phosphorothioate modification sites. The synthesized four PPA-grafted DNAs are assembled into a tetrahedron framework, which further associates with a programmed death ligand-1 (PD-L1) small interfering RNA (siRNA) linker through supramolecular self-assembly to form an siRNA and PPA copackaged nanogel. With dual therapeutic agents inside, the nanogel can photodynamically kill tumor cells and induce remarkable immunogenic cell death. Also, it simultaneously silences the PD-L1 expression of the tumor cells, which substantially promotes the antitumor immune response and leads to an enhanced antitumor efficacy in a synergistic fashion.
由于治疗药物内在的药效学差异,将多种药物包装到纳米载体中进行合理设计以实现协同癌症治疗仍然是一个挑战。特别是将小分子药物和大分子生物制剂结合在一起具有挑战性。在这里,我们成功地将原卟啉 IX(PPA)光敏剂接枝到 DNA 主链上预先设计的硫代磷酸酯修饰位点。合成的四个 PPA 接枝 DNA 组装成四面体框架,然后通过超分子自组装与程序性死亡配体-1(PD-L1)小干扰 RNA(siRNA)接头结合,形成 siRNA 和 PPA 共包封的纳米凝胶。纳米凝胶内部有两种治疗药物,既能进行光动力杀死肿瘤细胞,又能诱导明显的免疫原性细胞死亡。此外,它还能同时沉默肿瘤细胞的 PD-L1 表达,从而显著促进抗肿瘤免疫反应,并以协同方式增强抗肿瘤疗效。