The antitumour activities induced by pegylated liposomal cytochalasin D in murine models
文献类型: 外文期刊
第一作者: Huang, Feng-ying
作者: Huang, Feng-ying;Li, Yue-nan;Tan, Guang-hong;Guo, Jun-li;Wang, Hua;Huang, Yong-hao;Zhao, Huan-ge;Zhou, Song-lin;Li, Ling;Lin, Ying-ying;Huang, Feng-ying;Mei, Wen-li;Li, Yue-nan;Dai, Hao-fu;Huang, Feng-ying;Li, Yue-nan
作者机构:
关键词: Cytochalasin D;Pegylated liposome;Tumour angiogenesis;Apoptosis
期刊名称:EUROPEAN JOURNAL OF CANCER ( 影响因子:9.162; 五年影响因子:9.305 )
ISSN: 0959-8049
年卷期: 2012 年 48 卷 14 期
页码:
收录情况: SCI
摘要: Cytochalasin D targets actin and is ubiquitous in eukaryotic cells. When cytochalasin D is used as a cytotoxic agent in cancer therapy, it causes significant side effects. To prevent this, cytochalasin D can be encapsulated in polyethylene liposomes. In this study, high-performance liquid chromatography observation of the biodistribution of pegylated liposomal cytochalasin D in tumour-bearing mice showed that liposomal cytochalasin D could be conveniently dissolved in water for i.v. injection and that it specifically accumulated in tumour tissues, more than natural cytochalasin D did. The half-time of liposomal cytochalasin D in the plasma was also significantly longer than that of natural cytochalasin D (4 h versus 10 min). MTT 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay showed that liposomal cytochalasin D treatment could cause significant inhibition of cell proliferation in vitro in a manner similar to that of natural cytochalasin D. The antitumour activities of liposomal cytochalasin D were investigated in B16 melanoma, CT26 colorectal carcinoma and H22 hepatoma models, and the results indicated that liposomal cytochalasin D could significantly inhibit tumour growth and prolong survival in a manner similar to that of cisplatin. TUNEL-based apoptosis assays showed that liposomal cytochalasin D induced significant tumour cell apoptosis. Significant inhibition of tumour angiogenesis was observed in mice treated with liposomal cytochalasin D. In addition, no significant side effects were observed in mice treated with liposomal cytochalasin D. Our results show that liposomal cytochalasin D increases solubility and bioavailability, a lower incidence of side effects and improves antitumour effects, indicating its potential as a chemical agent for cancer therapy. (C) 2011 Elsevier Ltd. All rights reserved.
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