Temperature-dependent cell death patterns induced by functionalized gold nanoparticle photothermal therapy in melanoma cells

被引:245
|
作者
Zhang, Yujuan [1 ,2 ,3 ,4 ,7 ]
Zhan, Xuelin [1 ,2 ,3 ,4 ]
Xiong, Juan [5 ]
Peng, Shanshan [1 ,2 ,3 ,4 ,6 ]
Huang, Wei [1 ,2 ,3 ,4 ]
Joshi, Rakesh [6 ]
Cai, Ying [1 ,2 ,3 ,4 ]
Liu, Yanling [1 ,2 ,3 ,4 ]
Li, Rong [1 ,2 ,3 ]
Yuan, Keng [1 ,2 ,3 ,4 ]
Zhou, Nanjin [1 ,2 ,3 ,4 ]
Min, Weiping [1 ,2 ,3 ,4 ,6 ]
机构
[1] Nanchang Univ, Inst Immunotherapy, Nanchang, Jiangxi, Peoples R China
[2] Nanchang Univ, Coll Basic Med, Nanchang, Jiangxi, Peoples R China
[3] Jiangxi Acad Med Sci, Nanchang, Jiangxi, Peoples R China
[4] Jiangxi Prov Key Lab Immunotherapy, Nanchang, Jiangxi, Peoples R China
[5] Shenzhen Univ, Sch Med, Dept Prevent Med, Shenzhen, Peoples R China
[6] Univ Western Ontario, Dept Surg Pathol & Oncol, London, ON, Canada
[7] Harvard TH Chan Sch Publ Hlth, Dept Genet & Complex Dis, Boston, MA 02115 USA
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
基金
加拿大健康研究院;
关键词
DRUG-DELIVERY; IN-VITRO; NECROPTOSIS; CARCINOMA; APOPTOSIS; ABLATION; NANORODS; INHIBITOR; MECHANISM; AUTOPHAGY;
D O I
10.1038/s41598-018-26978-1
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Photothermal therapy (PTT) is a promising approach for cancer targeting therapy. However, the temperature-dependent killing of tumor cells in PTT remains unclear. In this study, we report necroptosis plays a role in the anti-tumor effects observed in gold nanorod (GNR)-mediated PTT in melanoma. We first synthesized gold nanorods with a targeting adaptor FA (GNRs-FA), which achieved high efficacy of targeted delivery to melanoma cells. We further demonstrated PTT, precipitated by GNRs-FA under the induction of near-infrared laser, was temperature-dependent. Furthermore, the photothermal killing of melanoma cells showed different patterns of cell death depending on varying temperature in PTT. In a lower temperature at 43 degrees C, the percentages of apoptosis, necroptosis and necrosis of tumor cells were 10.2%, 18.3%, and 17.6%, respectively, suggesting the cell killing is ineffective at lower temperatures. When the temperature increased to 49 degrees C, the cell death pattern switched to necrosis dominant (52.8%). Interestingly, when the PTT achieved a moderate temperature of 46 degrees C, necroptosis was significantly increased (35.1%). Additionally, GNRs-FA/PPT-mediated necroptosis was regulated by RIPK1 pathway. Taken together, this study is the first to demonstrate that temperature-dependent necroptosis is an important mechanism of inducing melanoma cell death in GNR-mediated PTT in addition to apoptosis and necrosis.
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页数:9
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