ROS-Responsive Nanoparticle Delivery of mRNA and Photosensitizer for Combinatorial Cancer Therapy

被引:32
|
作者
Zhou, Hui [1 ,2 ,5 ,6 ]
Liao, Yuqin [1 ]
Han, Xiangfei [5 ,6 ]
Chen, Dean Shuailin [5 ,6 ]
Hong, Xuechuan [1 ]
Zhou, Kun [3 ,4 ]
Jiang, Xingya [5 ,6 ]
Xiao, Yuling [5 ,6 ]
Shi, Jinjun [5 ,6 ]
机构
[1] Wuhan Univ, Zhongnan Hosp, Sch Pharmaceut Sci, Dept Cardiol, Wuhan 430071, Peoples R China
[2] Nanjing Univ Posts & Telecommun, State Key Lab Organ Elect & Informat Displays, Nanjing 210023, Peoples R China
[3] Nanjing Univ Posts & Telecommun, Inst Adv Mat IAM, Nanjing 210023, Peoples R China
[4] Harvard Med Sch, Boston Childrens Hosp, Vasc Biol Program, Boston, MA 02115 USA
[5] Harvard Med Sch, Ctr Nanomed, Brigham & Womens Hosp, Dept Anesthesiol, Boston, MA 02115 USA
[6] Harvard Med Sch, Brigham & Womens Hosp, Dept Anesthesiol Perioperat & Pain Med, Boston, MA 02115 USA
关键词
p53; mRNA delivery; ROS-responsive nanoparticles; Photodynamic therapy; Cancer; PHOTODYNAMIC THERAPY; PROTEINS;
D O I
10.1021/acs.nanolett.2c03784
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Messenger RNA (mRNA) therapy has shown tremendous potential for different diseases including cancer. While mRNA has been extensively used in cancer vaccine development as antigen or in cancer immunotherapy as immunomodulatory agent, the combination of mRNA therapy with photodynamic therapy has not been explored in cancer treatment. Herein, we report a reactive oxygen species (ROS)responsive polymeric nanoparticle (NP) platform for first-in-field codelivery of mRNA and photosensitizer for effective cancer treatment. We developed ROS-responsive oligomer-based polymeric NPs and applied them to test a combination of p53 mRNA and indocyanine green (ICG). The ROS-triggered disassembly of the NPs could promote mRNA translation efficiency, whereby p53 expression induced apoptosis of lung tumor cells. Meanwhile, the released ICG could lead to generation of ROS under 808 nm laser irradiation to induce photodynamic therapy. The NP codelivery of p53 mRNA and ICG demonstrated an effective and safe anti-tumor effect in a lung cancer model.
引用
收藏
页码:3661 / 3668
页数:8
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