Ultrasound-induced apoptosis in the presence of Sonazoid and associated alterations in gene expression levels: A possible therapeutic application

被引:33
作者
Furusawa, Yukihiro [2 ]
Zhao, Qing-Li [2 ]
Hassan, Mariame Ali [2 ]
Tabuchi, Yoshiaki [1 ]
Takasaki, Ichiro [1 ]
Wada, Shigehito [3 ]
Kondo, Takashi [2 ]
机构
[1] Toyama Univ, Div Mol Genet Res, Life Sci Res Ctr, Toyama 9300194, Japan
[2] Toyama Univ, Grad Sch Med & Pharmaceut Sci, Dept Radiol Sci, Toyama 9300194, Japan
[3] Toyama Univ, Grad Sch Med & Pharmaceut Sci, Dept Oral & Maxillofacial Surg, Toyama 9300194, Japan
关键词
Low-intensity ultrasound; Sonazoid; Apoptosis; GeneChip analysis; INTENSITY PULSED ULTRASOUND; FREE-RADICAL PRODUCTION; ECHO-CONTRAST AGENT; IDENTIFICATION; MICROBUBBLES; ENHANCEMENT; CELLS; COMBINATION; INHIBITION; MECHANISM;
D O I
10.1016/j.canlet.2009.06.029
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ultrasound (US) has been shown to induce apoptosis and cell lysis in cancer cells. In this study, we report on the potential of using Sonazoid, a new echo-contrast agent, that is chemically more stable and US-resistant in combination with US in cancer therapy. The biological effects and their mechanisms in the presence or absence of ultrasonic exposure in vitro were investigated. In addition, the impact of the agent on the expression levels of genes responsive to US was studied using global-scale microarrays and computational gene expression analysis tools. Our results show that the combination led to enhanced cell killing in the presence of 1 MHz acoustic field. The apoptosis induction was shown to be mediated by the mitochondrial pathway. The occurrence of US-induced DNA damage was also observed. Despite these findings, the agent at concentrations similar to those clinically used can be considered as well tolerated. Furthermore, Sonazoid enhanced expression of genes that related to apoptosis and are responsive to US, although it alone had almost no effect. These results indicate the potential of Sonazoid for US contrast enhancement as well as the possibility of its use in US-aided therapies. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:107 / 115
页数:9
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