| Literature DB >> 30773888 |
Smruthi Suryaprakash1, Yeh-Hsing Lao1, Hyeon-Yeol Cho2, Mingqiang Li1, Ha Yeun Ji1, Dan Shao1, Hanze Hu1, Chai Hoon Quek1, Dantong Huang1, Rachel L Mintz1, Juli R Bagó3, Shawn D Hingtgen3, Ki-Bum Lee2, Kam W Leong1,4.
Abstract
Mesenchymal stem cell (MSC) has been increasingly applied to cancer therapy because of its tumor-tropic capability. However, short retention at target tissue and limited payload option hinder the progress of MSC-based cancer therapy. Herein, we proposed a hybrid spheroid/nanomedicine system, comprising MSC spheroid entrapping drug-loaded nanocomposite, to address these limitations. Spheroid formulation enhanced MSC's tumor tropism and facilitated loading of different types of therapeutic payloads. This system acted as an active drug delivery platform seeking and specifically targeting glioblastoma cells. It enabled effective delivery of combinational protein and chemotherapeutic drugs by engineered MSC and nanocomposite, respectively. In an in vivo migration model, the hybrid spheroid showed higher nanocomposite retention in the tumor tissue compared with the single MSC approach, leading to enhanced tumor inhibition in a heterotopic glioblastoma murine model. Taken together, this system integrates the merits of cell- and nanoparticle- mediated drug delivery with the tumor-homing characteristics of MSC to advance targeted combinational cancer therapy.Entities:
Keywords: Mesenchymal stem cell; cell spheroid; glioblastoma; nanomedicine; targeted therapy
Mesh:
Year: 2019 PMID: 30773888 DOI: 10.1021/acs.nanolett.8b04697
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189