Arsenite-loaded nanoparticles inhibit the invasion and metastasis of a hepatocellular carcinoma: in vitro and in vivo study

被引:18
作者
Chi, Xiaoqin [1 ]
Yin, Zhenyu [1 ]
Jin, Jianbin [5 ]
Li, Hui [1 ,4 ]
Zhou, Jian [1 ,4 ]
Zhao, Zhenghuan [2 ,3 ]
Zhang, Sheng [1 ]
Zhao, Wenxiu [1 ]
Xie, Chengrong [1 ]
Li, Jie [1 ]
Feng, Min [1 ]
Lin, Hongyu [2 ,3 ]
Wang, Xiaomin [1 ]
Gao, Jinhao [2 ,3 ]
机构
[1] Xiamen Univ, Zhongshan Hosp, Xiamen Translat Med Key Lab Hepatobiliary & Pancr, Fujian Prov Key Lab Chron Liver Dis & Hepatocellu, Xiamen 361004, Peoples R China
[2] Xiamen Univ, Coll Chem & Chem Engn, State Key Lab Phys Chem Solid Surfaces, Key Lab Chem Biol Fujian Prov, Xiamen 361005, Peoples R China
[3] Xiamen Univ, Coll Chem & Chem Engn, Dept Biol Chem, Xiamen 361005, Peoples R China
[4] Fudan Univ, Liver Canc Inst, Zhongshan Hosp, Key Lab Carcinogenesis & Canc Invas,Minist Educ, Shanghai 200032, Peoples R China
[5] Yiwu Cent Hosp, Yiwu 322000, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
hepatocellular carcinoma; nano-drugs; arsenic trioxide; migration; metastasis; in vivo; CIRCULATING TUMOR-CELLS; TRIGGERED RELEASE; PROGNOSTIC VALUE; DELIVERY-SYSTEM; CANCER-CELLS; TRIOXIDE; MICROTUBULES; CYTOTOXICITY; RECURRENCE; ACTIVATION;
D O I
10.1088/1361-6528/aa8791
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Postoperative recurrence and metastasis are the major problems for the current treatment of hepatocellular carcinomas (HCC) in the clinic, including hepatectomy and liver transplantation. Here, we report that arsentic-loaded nanoparticles (ALNPs) are able to reduce the invasion of HCC cells in vitro, and, more importantly, can strongly suppress the invasion and metastasis of HCC in vivo without adverse side effects. Compared to free drug arsenic trioxide, ALNPs can deliver the drug into cancer cells more efficiently, destroy the structure of microtubules and reduce the aggregation of microfilaments in cell membranes more significantly. Furthermore, our results also reveal that tumor cells in murine blood were reduced remarkably after intravenous injection of ALNPs, indicating that this nano-drug may efficiently kill circulating tumor cells in vivo. In conclusion, our nano-drug ALNPs have great potential for the suppression of metastasis of HCC, which may open up a new avenue for the effective treatment of HCC without metastasis and recurrence.
引用
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页数:11
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共 48 条
[1]  
[Anonymous], 2018, ANTI-CANCER DRUG, DOI [DOI 10.3322/caac.20115, DOI 10.1097/CAD.0000000000000617]
[2]   Mutational studies on single circulating tumor cells isolated from the blood of inflammatory breast cancer patients [J].
Bingham, Catherine ;
Fernandez, Sandra V. ;
Fittipaldi, Patricia ;
Dempsey, Paul W. ;
Ruth, Karen J. ;
Cristofanilli, Massimo ;
Alpaugh, R. Katherine .
BREAST CANCER RESEARCH AND TREATMENT, 2017, 163 (02) :219-230
[3]   A Perspective on Cancer Cell Metastasis [J].
Chaffer, Christine L. ;
Weinberg, Robert A. .
SCIENCE, 2011, 331 (6024) :1559-1564
[4]   Development of a hybrid paclitaxel-loaded arsenite nanoparticle (HPAN) delivery system for synergistic combined therapy of paclitaxel-resistant cancer [J].
Chen, Fei-yan ;
Zhang, Yu ;
Chen, Xiang-yu ;
Li, Jia-qian ;
Xiao, Xiao-ping ;
Yu, Lu-lu ;
Tang, Qun .
JOURNAL OF NANOPARTICLE RESEARCH, 2017, 19 (04)
[5]   Inorganic phosphate-triggered release of anti-cancer arsenic trioxide from a self-delivery system: an in vitro and in vivo study [J].
Chen, Fei-yan ;
Yi, Jing-wei ;
Gu, Zhe-jia ;
Tang, Bin-bing ;
Li, Jian-qi ;
Li, Li ;
Kulkarni, Padmakar ;
Liu, Li ;
Mason, Ralph P. ;
Tang, Qun .
NANOSCALE, 2016, 8 (11) :6094-6100
[6]   Lipid encapsulation of arsenic trioxide attenuates cytotoxicity and allows for controlled anticancer drug release [J].
Chen, Haimei ;
MacDonald, Robert C. ;
Li, Shuyou ;
Krett, Nancy L. ;
Rosen, Steven T. ;
O'Halloran, Thomas V. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (41) :13348-13349
[7]   Biofunctionalized magnetic nanospheres-based cell sorting strategy for efficient isolation, detection and subtype analyses of heterogeneous circulating hepatocellular carcinoma cells [J].
Chen, Lan ;
Wu, Ling-Ling ;
Zhang, Zhi-Ling ;
Hu, Jiao ;
Tang, Man ;
Qi, Chu-Bo ;
Li, Na ;
Pang, Dai-Wen .
BIOSENSORS & BIOELECTRONICS, 2016, 85 :633-640
[8]   Nanoprobes for in vitro diagnostics of cancer and infectious diseases [J].
Chi, Xiaoqin ;
Huang, Dengtong ;
Zhao, Zhenghuan ;
Zhou, Zijian ;
Yin, Zhenyu ;
Gao, Jinhao .
BIOMATERIALS, 2012, 33 (01) :189-206
[9]   Continuous Improvement of Survival Outcomes of Resection of Hepatocellular Carcinoma A 20-Year Experience [J].
Fan, Sheung Tat ;
Lo, Chung Mau ;
Poon, Ronnie T. P. ;
Yeung, Chun ;
Liu, Chi Leung ;
Yuen, Wai Key ;
Lam, Chi Ming ;
Ng, Kelvin K. C. ;
Chan, See Ching .
ANNALS OF SURGERY, 2011, 253 (04) :745-758
[10]   Inhibition of Cancer Cell Migration by Multiwalled Carbon Nanotubes [J].
Garcia-Hevia, Lorena ;
Valiente, Rafael ;
Fernandez-Luna, Jose L. ;
Flahaut, Emmanuel ;
Rodriguez-Fernandez, Lidia ;
Villegas, Juan C. ;
Gonzalez, Jesus ;
Fanarraga, Monica L. .
ADVANCED HEALTHCARE MATERIALS, 2015, 4 (11) :1640-1644