Two Zn(ii) coordination polymers with anticancer drug norcantharidin as ligands for cancer chemotherapy

被引:13
作者
Wang, Jia [1 ]
Huang, Xiange [2 ]
Li, Hegen [2 ]
Yan, Deyue [1 ]
Huang, Wei [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, State Key Lab Met Matrix Composites, Shanghai 200240, Peoples R China
[2] Shanghai Univ Tradit Chinese Med, Longhua Hosp, Shanghai 200032, Peoples R China
关键词
METAL-ORGANIC FRAMEWORK; APOPTOSIS; METASTASIS; ADSORPTION; CARCINOMA; INVASION; CASPASE; CELLS; TUMOR;
D O I
10.1039/d2dt00300g
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Here two Zn(ii) coordination polymers [Zn-20(DMCA)(12)]O-12 (DMCA = demethylcantharic acid, DMCA-Zn1) and [Zn(DMCA)](H2O)(2) (DMCA-Zn2) are synthesized from a broad-spectrum anticancer drug norcantharidin (NCTD) and Zn(NO3)(2)center dot 6H(2)O under solvothermal conditions. By mechanical grinding with a biocompatible polymeric surfactant F127, ultrasonic treatment and filtration, DMCA-Zn1 and DMCA-Zn2 can be transformed into stable nanoparticles (DMCA-Zn1 NPs and DMCA-Zn2 NPs) suspended in water with average diameters of around 190 nm and 162 nm for drug delivery. The in vitro evaluation indicates that DMCA-Zn1 NPs and DMCA-Zn2 NPs can enter into HepG2 and Hep3B cancer cells via endocytosis and inhibit their proliferation. Meanwhile they exhibit relatively low toxicity to L927 normal cells. The in vivo evaluation confirms that DMCA-Zn1 NPs and DMCA-Zn2 NPs can more effectively inhibit the growth of Hep3B tumors with relatively few side effects compared with free NCTD. This approach can be extended to other anticancer drugs to construct nanodrug delivery systems for cancer treatment.
引用
收藏
页码:5624 / 5634
页数:11
相关论文
共 49 条
[1]  
Bray F, 2018, CA-CANCER J CLIN, V68, P394, DOI [10.3322/caac.21492, 10.3322/caac.21609]
[2]   Norcantharidin induce apoptosis in human nasopharyngeal carcinoma through caspase and mitochondrial pathway [J].
Chen, Andy Wei-Ge ;
Tseng, Yen-Shuo ;
Lin, Chia-Chieh ;
Hsi, Yi-Ting ;
Lo, Yu-Sheng ;
Chuang, Yi-Ching ;
Lin, Shu-Hui ;
Yu, Chia-Yun ;
Hsieh, Ming-Ju ;
Chen, Mu-Kuan .
ENVIRONMENTAL TOXICOLOGY, 2018, 33 (03) :343-350
[3]   Knockdown of interferon-stimulated gene 15 affects the sensitivity of hepatocellular carcinoma cells to norcantharidin [J].
Chen, Baoxiang ;
Jin, Shuqiang ;
Bai, Bin ;
Li, Zhi ;
Ni, Caifang ;
Liu, Yansen .
EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2019, 18 (05) :3751-3758
[4]   Synthesis and crystal structure of a new Zn(II) complex with anti-leukemia activity [J].
Chen, Shang-Liang ;
Liu, Xiao-Yan ;
Li, Shao-Chang ;
Wu, Chaoyu ;
Li, Zhi-Yi ;
Li, Ting-Ting .
INORGANIC AND NANO-METAL CHEMISTRY, 2021, 51 (02) :224-229
[5]   Protein phosphatase 5 promotes hepatocarcinogenesis through interaction with AMP-activated protein kinase [J].
Chen, Yao-Li ;
Hung, Man-Hsin ;
Chu, Pei-Yi ;
Chao, Tzu-I ;
Tsai, Ming-Hsien ;
Chen, Li-Ju ;
Hsiao, Yung-Jen ;
Shih, Chih-Ting ;
Hsieh, Feng-Shu ;
Chen, Kuen-Feng .
BIOCHEMICAL PHARMACOLOGY, 2017, 138 :49-60
[6]   Inhibitory effect of norcantharidin, a derivative compound from blister beetles, on tumor invasion and metastasis in CT26 colorectal adenocarcinorna cells [J].
Chen, YJ ;
Shieh, CJ ;
Tsai, TH ;
Kuo, CD ;
Ho, LT ;
Liu, TY ;
Liao, HF .
ANTI-CANCER DRUGS, 2005, 16 (03) :293-299
[7]   Effector mechanisms of norcantharidin-induced mitotic arrest and apoptosis in human hepatoma cells [J].
Chen, YN ;
Chen, JC ;
Yin, SC ;
Wang, GS ;
Tsauer, W ;
Hsu, SF ;
Hsu, SL .
INTERNATIONAL JOURNAL OF CANCER, 2002, 100 (02) :158-165
[8]   ANGIOGENESIS IN CANCER, VASCULAR, RHEUMATOID AND OTHER DISEASE [J].
FOLKMAN, J .
NATURE MEDICINE, 1995, 1 (01) :27-31
[9]   Ultrahigh Porosity in Metal-Organic Frameworks [J].
Furukawa, Hiroyasu ;
Ko, Nakeun ;
Go, Yong Bok ;
Aratani, Naoki ;
Choi, Sang Beom ;
Choi, Eunwoo ;
Yazaydin, A. Oezguer ;
Snurr, Randall Q. ;
O'Keeffe, Michael ;
Kim, Jaheon ;
Yaghi, Omar M. .
SCIENCE, 2010, 329 (5990) :424-428
[10]   Norcantharidin inhibits IL-6-induced epithelial-mesenchymal transition via the JAK2/STAT3/TWIST signaling pathway in hepatocellular carcinoma cells [J].
Gao, Yebo ;
Li, Weidong ;
Liu, Rui ;
Guo, Qiujun ;
Li, Jie ;
Bao, Yanju ;
Zheng, Honggang ;
Jiang, Shulong ;
Hua, Baojin .
ONCOLOGY REPORTS, 2017, 38 (02) :1224-1232