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Ultrasound-stimulated Microbubbles for Treatment of Pancreatic Cancer Cells with Radiation and Nanoparticles: In vitro Study
被引:0
|作者:
Nakayama, Masao
[1
,2
,4
]
Noda, Ayaha
[3
]
Akasaka, Hiroaki
[1
,5
]
Tominaga, Takahiro
[3
]
McCorkell, Giulia
[4
]
Geso, Moshi
[4
]
Sasaki, Ryohei
[1
]
机构:
[1] Kobe Univ, Grad Sch Med, Div Radiat Oncol, 7-5-2 Kusunokicho,Chuou Ku, Kobe 6500017, Japan
[2] Kita Harima Med Ctr, Div Radiat Therapy, Ono, Hyogo, Japan
[3] Hiroshima Int Univ, Fac Hlth Sci, Dept Clin Radiol, Hiroshima, Japan
[4] RMIT Univ, Sch Hlth & Biomed Sci, Discipline Med Radiat, Bundoora, Australia
[5] Univ Melbourne, Dept Chem Engn, Parkville, Vic, Australia
基金:
日本学术振兴会;
关键词:
Microbubbles;
nanoparticles;
radiation therapy;
radiosensitizer;
ultrasound;
CONTRAST AGENTS;
THERAPY;
SONOPORATION;
RADIOSENSITIZATION;
PARAMETERS;
APOPTOSIS;
TUMORS;
D O I:
10.4103/jmp.jmp_30_24
中图分类号:
R8 [特种医学];
R445 [影像诊断学];
学科分类号:
1002 ;
100207 ;
1009 ;
摘要:
Purpose: This study aims to investigate the radiation enhancement effects of ultrasound-stimulated microbubbles (USMB) with X-rays and nanoparticles on pancreatic cancer cells in vitro. Methods: Sonazoid (TM) microbubbles were used for USMB treatment with a commercially available ultrasound unit. The characterization of the microbubbles before and after ultrasound exposure with different mechanical parameters was evaluated microscopically. Two pancreatic cancer cell lines, MIAPaCa-2 and PANC-1, were treated with different concentrations of microbubbles in combination with 150 kVp X-rays and hydrogen peroxide-modified titanium dioxide nanoparticles. Cell viability was evaluated using a water-soluble tetrazolium dye and a colony formation assay. In addition, intracellular reactive oxygen species (ROS) induced by the combined treatment were assessed. Results: The number of burst microbubbles increased with ultrasound's higher mechanical index and the exposure time. A significant radiation enhancement effect with a significant increase in ROS levels was observed in MIAPaCa-2 cells treated with USMB and 6 Gy X-rays, whereas it was not significant in PANC-1 cells treated with the same. When a higher concentration of USMB was applied with X-rays, no radiation enhancement effects were observed in either cell line. Moreover, there was no radiation enhancement effect by USMB between cells treated with and without nanoparticles. Conclusions: The results indicate that USMB treatment can additively enhance the therapeutic efficacy of radiation therapy on pancreatic cancer cells, while the synergistic enhancement effects are likely to be cell type and microbubble concentration dependent. In addition, USMB did not improve the efficacy of nanoparticle-induced radiosensitization in the current setting.
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页码:326 / 334
页数:9
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