| Literature DB >> 27356586 |
Jiang Wu, Ying Liu, Yuxia Tang, Shouju Wang, Chunyan Wang, Yanjun Li, Xiaodan Su1, Jihong Tian2, Ying Tian, Jing Pan, Yunyan Su, Hong Zhu, Zhaogang Teng3, Guangming Lu3.
Abstract
Mesenchymal stem cells (MSCs) have attracted increasing attention as vehicles for cancer treatment. Herein, MSC-based synergistic oncotherapy strategy is presented for the first time. To achieve this goal, yolk-shell structured gold nanorod embedded hollow periodic mesoporous organosilica nanospheres (GNR@HPMOs) with high paclitaxel (PTX) loading capability and excellent photothermal transfer ability upon near-infrared (NIR) light irradiation are first prepared. Cytotoxicity and migration assays show that the viability and tumor-homing capability of MSCs are well-retained after internalization of high content of PTX loaded GNR@HPMOs (denoted as GNR@HPMOs-PTX). In vitro experiments show the GNR@HPMOs-PTX loaded MSCs (GNR@HPMOs-PTX@MSCs) possess synergistic chemo-photothermal killing effects for breast cancer cells. Also, photoacoustic imaging shows that the MSCs can improve dispersion and distribution in tumor tissue for GNR@HPMOs-PTX after intratumoral injection. In vivo experiments in breast cancer model of nude mice further demonstrate that the GNR@HPMOs-PTX@MSCs significantly inhibit tumor growth, suggesting their great potential for synergistic therapy of cancer.Entities:
Keywords: breast cancer; gold nanorods; mesenchymal stem cells; periodic mesoporous organosilica; synergistic therapy
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Year: 2016 PMID: 27356586 DOI: 10.1021/acsami.6b05677
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229