Department of Pharmacy, Jiangsu Cancer Hospital, the Affiliated Cancer Hospital of Nanjing Medical University, Jiangsu Institute of Cancer Research, 42 Baiziting Road, Nanjing 210009, China.
Key Laboratory of Flexible Electronics (KLOFE), School of Flexible Electronics (Future Technologies) & Institute of Advanced Materials (IAM), Nanjing Tech University (NanjingTech), 30 South Puzhu Road, Nanjing 211816, China.
ACS Appl Mater Interfaces. 2024 Aug 28;16(34):45523-45536. doi: 10.1021/acsami.4c08842. Epub 2024 Aug 14.
Triple-negative breast cancer (TNBC) is a subtype of breast cancer that carries the worst prognosis and lacks specific therapeutic targets. To achieve accurate "cargos" delivery at the TNBC site, we herein constructed a novel biomimetic nano-Trojan horse integrating chemotherapy with gene therapy for boosting TNBC treatment. Briefly, we initially introduce the diselenide-bond-containing organosilica moieties into the framework of mesoporous silica nanoparticles (MONs), thereby conferring biodegradability to intratumoral redox conditions in the obtained MON. Subsequently, doxorubicin (Dox) and therapeutic miR-34a are loaded into MON, thus achieving the combination of chemotherapy and gene-therapy. After homologous tumor cell membrane coating, the ultimate homologous tumor cell-derived biomimetic nano-Trojan horse (namely, MON@Dox@miR-34a@CM) can selectively enter the tumor cells in a stealth-like fashion. Notably, such a nanoplatform not only synergistically eradicated the tumor but also inhibited the proliferation of breast cancer stem-like cells (BCSCs) and . With the integration of homologous tumor cell membrane-facilitated intratumoral accumulation, excellent biodegradability, and synergistic gene-chemotherapy, our biomimetic nanocarriers hold tremendous promise for the cure of TNBC in the future.
三阴性乳腺癌(TNBC)是乳腺癌的一种亚型,预后最差,缺乏特定的治疗靶点。为了在 TNBC 部位实现准确的“货物”递送,我们构建了一种新型仿生纳米木马,将化疗与基因治疗相结合,以增强 TNBC 的治疗效果。简而言之,我们首先将含有二硒键的有机硅烷部分引入介孔硅纳米颗粒(MONs)的框架中,从而使获得的 MON 能够在肿瘤内的氧化还原条件下生物降解。随后,将阿霉素(Dox)和治疗性 miR-34a 装载到 MON 中,从而实现化疗和基因治疗的联合。经过同源肿瘤细胞膜包覆后,最终的同源肿瘤细胞衍生仿生纳米木马(即 MON@Dox@miR-34a@CM)可以以一种类似隐身的方式选择性进入肿瘤细胞。值得注意的是,这种纳米平台不仅协同消除了肿瘤,还抑制了乳腺癌干细胞样细胞(BCSCs)的增殖和 。通过同源肿瘤细胞膜介导的肿瘤内积累、优异的生物降解性和协同的基因-化疗作用,我们的仿生纳米载体有望在未来治愈 TNBC。