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Multilayer photodynamic therapy for highly effective and safe cancer treatment
被引:19
|作者:
Yang, Ling
[1
]
Zhang, Shaojuan
[2
]
Ling, Xiaoxi
[2
]
Shao, Pin
[2
]
Jia, Ningyang
[3
]
Bai, Mingfeng
[2
,4
,5
,6
]
机构:
[1] Fudan Univ, Sch Basic Med Sci, Dept Cellular & Genet Med, Shanghai 200032, Peoples R China
[2] Univ Pittsburgh, Dept Radiol, 100 Technol Dr, Pittsburgh, PA 15219 USA
[3] Second Mil Med Univ, Eastern Hepatobiliary Surg Hosp, Dept Radiol, Shanghai 200438, Peoples R China
[4] Univ Pittsburgh, Dept Med, 3501 Fifth Ave, Pittsburgh, PA 15213 USA
[5] Univ Pittsburgh, Dept Bioengn, Pittsburgh, PA 15261 USA
[6] Univ Pittsburgh, Inst Canc, Pittsburgh, PA 15232 USA
关键词:
Photodynamic therapy;
CB2;
receptor;
TSPO;
Synergistic;
Combination therapy;
PERIPHERAL BENZODIAZEPINE-RECEPTOR;
CANNABINOID CB2 RECEPTOR;
NEGATIVE BREAST-CANCER;
CELL-CYCLE ARREST;
IN-VIVO;
TRANSLOCATOR PROTEIN;
DRUG-RESISTANCE;
ENDOCANNABINOID SYSTEM;
CARCINOMA-CELLS;
NECK CANCERS;
D O I:
10.1016/j.actbio.2017.03.012
中图分类号:
R318 [生物医学工程];
学科分类号:
0831 ;
摘要:
Recent efforts to develop tumor-targeted photodynamic therapy (PDT) photosensitizers (PSs) have greatly advanced the potential of PDT in cancer therapy, although complete eradication of tumor cells by PDT alone remains challenging. As a way to improve PDT efficacy, we report a new combinatory PDT therapy technique that specifically targets multilayers of cells. Simply mixing different PDT PSs, even those that target distinct receptors (this may still lead to similar cell-killing pathways), may not achieve ideal therapeutic outcomes. Instead, significantly improved outcomes likely require synergistic therapies that target various cellular pathways. In this study, we target two proteins upregulated in cancers: the cannabinoid CB2 receptor (CB2R, a G-protein coupled receptor) and translocator protein (TSPO, a mitochondria membrane receptor). We found that the CB2R-targeted PS, IR700DX-mbc94, triggered necrotic cell death upon light irradiation, whereas PDT with the TSPO-targeted IR700DX-6T agent led to apoptotic cell death. Both PSs significantly inhibited tumor growth in vivo in a target-specific manner. As expected, the combined CB2R- and TSPO-PDT resulted in enhanced cell killing efficacy and tumor inhibition with lower drug dose. The median survival time of animals with multilayer PDT treatment was extended by as much as 2.8-fold over single PDT treatment. Overall, multilayer PDT provides new opportunities to treat cancers with high efficacy and low side effects. Statement of Significance Photodynamic therapy (PDT) is increasingly used as a minimally invasive, controllable and effective therapeutic procedure for cancer treatment. However, complete eradication of tumor cells by PDT alone remains challenging. In this study, we investigate the potential of multilayer PDT in cancer treatment with high efficacy and low side effects. Through PDT targeting two cancer biomarkers located at distinct subcellular localizations, remarkable synergistic effects in cancer cell killing and tumor inhibition were observed in both in vitro and in vivo experiments. This strategy may be widely applied to treat various cancer types by using strategically designed PDT photosensitizers that target corresponding upregulated receptors at tactical subcellular localization. (C) 2017 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
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页码:271 / 280
页数:10
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