| Literature DB >> 26004286 |
Wei Rao1,2, Hai Wang1,2,3, Jianfeng Han3,4, Shuting Zhao1,2, Jenna Dumbleton1,2, Pranay Agarwal1,2, Wujie Zhang5, Gang Zhao6, Jianhua Yu3,4, Debra L Zynger7, Xiongbin Lu8, Xiaoming He1,2,3.
Abstract
Tumor reinitiating cancer stem-like cells are responsible for cancer recurrence associated with conventional chemotherapy. We developed a doxorubicin-encapsulated polymeric nanoparticle surface-decorated with chitosan that can specifically target the CD44 receptors of these cells. This nanoparticle system was engineered to release the doxorubicin in acidic environments, which occurs when the nanoparticles are localized in the acidic tumor microenvironment and when they are internalized and localized in the cellular endosomes/lysosomes. This nanoparticle design strategy increases the cytotoxicity of the doxorubicin by six times in comparison to the use of free doxorubicin for eliminating CD44(+) cancer stem-like cells residing in 3D mammary tumor spheroids (i.e., mammospheres). We further show these nanoparticles reduced the size of tumors in an orthotopic xenograft tumor model with no evident systemic toxicity. The development of nanoparticle system to target cancer stem-like cells with low systemic toxicity provides a new treatment arsenal for improving the survival of cancer patients.Entities:
Keywords: CD44; EPR; cancer stem-like cell; chitosan; nanoparticle; targeting
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Year: 2015 PMID: 26004286 DOI: 10.1021/nn506928p
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881