Ultrasound-Activated Microbubble Cancer Therapy: Ceramide Production Leading to Enhanced Radiation Effect in vitro

被引:38
作者
Nofiele, J. I. T. [1 ,2 ,3 ]
Karshafian, R. [2 ,3 ]
Furukawa, M. [1 ,2 ]
Al Mahrouki, A. [1 ,2 ]
Giles, A. [1 ,2 ]
Wong, S. [1 ,4 ,5 ]
Czarnota, G. J. [1 ,2 ,4 ,5 ]
机构
[1] Sunnybrook Hlth Sci Ctr, Toronto, ON M4N 3M5, Canada
[2] Sunnybrook Res Inst, Toronto, ON M4N 3M5, Canada
[3] Ryerson Univ, Dept Phys, Toronto, ON M5B 2K3, Canada
[4] Univ Toronto, Dept Radiat Oncol, Toronto, ON M4N 3M5, Canada
[5] Univ Toronto, Dept Med Biophys, Toronto, ON M4N 3M5, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Ceramide; Microbubbles; Ultrasound; Radiation; Asmase; APOPTOSIS;
D O I
10.7785/tcrt.2012.500253
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Blood vessels within tumours represent a key component for cancer cell survival. Disruption of these vessels can be achieved by inducing vascular endothelial-cell apoptosis. Moreover, endothelial cell apoptosis has been proven to be enhanced by ceramide-increasing drugs. Herein, we introduce a novel therapeutic approach which uses ultrasound-stimulated microbubbles used in combination with radiation to cause a rapid accumulation of ceramide in endothelial cells in-vitro. We also test this modality directly with other cell types as a general method of killing cancer cells. Human umbilical vein endothelial cells (HUVEC), acute myeloid leukemia cells (AML), murine fibrosarcoma cells (KHT-C), prostate cancer cells (PC3), breast cancer cells (MDA-MB-231) and astrocytes were used to evaluate this mechanism of inducing cell death. Survival was measured by clonogenic assays, and ceramide content was detected using immunohistochemistry. Exposure of cell types to ultrasound-stimulated bubbles alone resulted in increases in ceramide for all cell types and survivals of 12 +/- 2%, 65 +/- 5%, 83 2%, 58 +/- 4%, 58 +/- 3%, 18 +/- 7% for HUVEC, AML, PC3, MDA, KHT-C and astrocyte cells, respectively. Results from selected cell types involving radiation treatments indicated additive treatment enhancements and increases in intracellular ceramide content one hour after exposure to ultrasound-activated microbubbles and radiation. Endothelial cell survival decreased from 8 +/- 1% after 2 Gy of radiation treatment alone and from 12 +/- 2% after ultrasound and microbubbles alone, to 1 +/- 1% with combined treatment. In Asmase +/+ astrocytes, survival decreased from 56 +/- 2% after 2 Gy radiation alone and from 17 +/- 7% after ultrasound and microbubbles alone, to 5 +/- 2% when combined. Using ASMase deficient astrocytes (Asmase -/-) and Sphingosine-1-phosphate (S1P), we also demonstrate that ultrasound-activated microbubbles stimulate ASMase activity and ceramide production. These findings suggest that ultrasound-stimulated microbubbles could be used as a new biomechanical method to enhance the effects of radiation.
引用
收藏
页码:53 / 60
页数:8
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