Acridine orange exhibits photodamage in human bladder cancer cells under blue light exposure

被引:21
|
作者
Lin, Yi-Chia [1 ,2 ]
Lin, Ji-Fan [3 ]
Tsai, Te-Fu [1 ,2 ]
Chen, Hung-En [1 ]
Chou, Kuang-Yu [1 ,2 ]
Yang, Shan-Che [3 ]
Tang, Ya-Ming [3 ]
Hwang, Thomas I. -Sheng [1 ,2 ]
机构
[1] Shin Kong Wu Ho Su Mem Hosp, Dept Urol, Taipei, Taiwan
[2] Fu Jen Catholic Univ, Sch Med, New Taipei, Taiwan
[3] Shin Kong Wu Ho Su Mem Hosp, Cent Lab, Taipei, Taiwan
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
关键词
PHOTODYNAMIC THERAPY; PROTECTIVE AUTOPHAGY; NUCLEIC-ACIDS; INHIBITION; DAMAGE; MANAGEMENT; APOPTOSIS;
D O I
10.1038/s41598-017-13904-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Human bladder cancer (BC) cells exhibit a high basal level of autophagic activity with accumulation of acridine-orange(AO)-stained acidic vesicular organelles. The rapid AO relocalization was observed in treated BC cells under blue-light emission. To investigate the cytotoxic effects of AO on human BC cell lines under blue-light exposure, human immortalized uroepithelial (SV-Huc-1) and BC cell lines (5637 and T24) were treated with indicated concentrations of AO or blue-light exposure alone and in combination. The cell viability was then determined using WST-1, time-lapse imaging with a Cytosmart System and continuous quantification with a multi-mode image-based reader. Treatment of AO or blue-light exposure alone did not cause a significant loss of viability in BC cells. However, AO exhibited a dose-dependent increment of cytotoxicity toward BC cells under blue-light exposure. Furthermore, the tumor formation of BC cells with treatment was significantly reduced when evaluated in a mouse xenograft model. The photodamage caused by AO was nearly neglected in SV-Huc-1 cells, suggesting a differential effect of this treatment between cancer and normal cells. In summary, AO, as a photosensitizer, disrupts acidic organelles and induces cancer cell death in BC cells under blue-light irradiation. Our findings may serve as a novel therapeutic strategy against human BC.
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页数:11
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