| Literature DB >> 33089613 |
Zhaoran Wang1,2, Linlin Song1, Qing Liu1, Run Tian1,2, Yingxu Shang1, Fengsong Liu1,2, Shaoli Liu1, Shuai Zhao1,2, Zihong Han1,2, Jiashu Sun1,2, Qiao Jiang1,2, Baoquan Ding1,2.
Abstract
Using the DNA origami technique, we constructed a DNA nanodevice functionalized with small interfering RNA (siRNA) within its inner cavity and the chemotherapeutic drug doxorubicin (DOX), intercalated in the DNA duplexes. The incorporation of disulfide bonds allows the triggered mechanical opening and release of siRNA in response to intracellular glutathione (GSH) in tumors to knockdown genes key to cancer progression. Combining RNA interference and chemotherapy, the nanodevice induced potent cytotoxicity and tumor growth inhibition, without observable systematic toxicity. Given its autonomous behavior, exceptional designability, potent antitumor activity and marked biocompatibility, this DNA nanodevice represents a promising strategy for precise drug design for cancer therapy.Entities:
Keywords: DNA origami; cancer therapy; drug delivery; nanodevice; siRNA delivery
Mesh:
Substances:
Year: 2020 PMID: 33089613 DOI: 10.1002/anie.202009842
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336