Photothermolysis of glioblastoma stem-like cells targeted by carbon nanotubes conjugated with CD133 monoclonal antibody

被引:163
作者
Wang, Chung-Hao [2 ]
Chiou, Shih-Hwa [3 ,4 ]
Chou, Chen-Pin [3 ,5 ]
Chen, Yu-Chih [3 ]
Huang, Yao-Jhang [2 ]
Peng, Ching-An [1 ]
机构
[1] Michigan Technol Univ, Dept Chem Engn, Houghton, MI 49931 USA
[2] Natl Taiwan Univ, Dept Chem Engn, Taipei 10764, Taiwan
[3] Taipei Vet Gen Hosp, Dept Educ & Res, Taipei, Taiwan
[4] Natl Yang Ming Univ, Inst Clin Med, Taipei 112, Taiwan
[5] Kaohsiung Vet Gen Hosp, Dept Radiol, Kaohsiung, Taiwan
关键词
Glioblastoma; Cancer stem-like cells; CD133; Single-walled carbon nanotubes; Near-infrared laser; IDENTIFICATION; TEMOZOLOMIDE; DESTRUCTION; TUMORS;
D O I
10.1016/j.nano.2010.06.010
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
CD133(+) cells in glioblastoma (GBM) display cancer stem cell-like properties and have been considered as the culprit of tumor recurrence, justifying exploration of potential therapeutic modalities targeting CD133(+) cancer stem-like cells (CSCs). For photothermolysis studies, GBM-CD133(+) and GBM-CD133-cells mixed with various ratios were challenged with single-walled carbon nanotubes (SWNTs) conjugated with CD133 monoclonal antibody (anti-CD133) and then irradiated with near-infrared laser light. Results show that GBM-CD133(+) cells were selectively targeted and eradicated, whereas GBM-CD133-cells remained viable. In addition, in vitro tumorigenic and self-renewal capability of GBM-CD133(+) treated with localized hyperthermia was significantly blocked. Furthermore, GBM-CD133(+) cells pretreated with anti-CD133-SWNTs and irradiated by near-infrared laser 2 days after xenotransplantation in nude mice did not exhibit sustainability of CSC features for tumor growth. Taken altogether, our studies demonstrated that anti-CD133-SWNTs have the potential to be utilized as a thermal-coupling agent to effectively target and destroy GBM CSCs in vitro and in vivo. From the Clinical Editor: Glioblastoma remains one of the most notorious cancer from the standpoint of recurrence and overall resistance to therapy. CD133+ stem cells occur among GBM cells, and may be responsible for the huge recurrence risk. This paper discusses a targeted elimination method of these cells, which may enable more efficient therapy in an effort to minimize or prevent recurrence. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:69 / 79
页数:11
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