Ultrasound sensitizes chemotherapy in chemoresistant ovarian cancers

被引:0
作者
Lou, Yi [1 ]
Zhang, Yi [2 ]
He, Haining [2 ]
Liu, Yingfen [2 ]
Huang, Ping [3 ]
Yu, Tinghe [1 ,2 ]
机构
[1] Chongqing Med Univ, Inst Life Sci, Chongqing, Peoples R China
[2] Sichuan Univ, W China Univ Hosp 2, W China Inst Women & Childrens Hlth, Lab Biomed Ultrason, Chengdu 610064, Peoples R China
[3] Chongqing Med Univ, Affiliated Hosp 1, Dept Gen Surg, Chongqing, Peoples R China
关键词
Chemoresistance; ovarian cancer; ultrasound; sonochemotherapy; targeted therapy; CARCINOMA CELL-LINE; ADRIAMYCIN RESISTANCE; CISPLATIN; DRUG; MICROBUBBLES; COMBINATION; MECHANISMS; REVERSAL; THERAPY;
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Chemotherapy resistance is still a great challenge to the management of ovarian cancers. Using SKOV3/ADR or COC1/DDP subline as a model of adriamycin- or cisplatin-resistance, ultrasonic chemosensitization was investigated. The addition of noncytotoxic insonation led to a higher cell-death rate as compared with a drug alone. Ultrasound sensitized chemotherapy via increasing intracellular drug accumulation, enhancing drug-induced apoptosis and decreasing the threshold dose for cell apoptosis/necrosis. Ultrasound exposure enhanced cisplatin-induced DNA breakages in COC1/DDP cells but did not decrease the level of glutathione-S-transferase. Chemosensitization attributable to insonation was mostly mediated by cavitation. Ultrasonic chemotherapy had the property of a targeted treatment, in that the dose-anticancer effect and dose-toxicity curves differed from those in conventional chemotherapy. The findings indicated that ultrasound was a non-drug modality for sensitizing chemotherapy in refractory ovarian cancers.
引用
收藏
页码:12047 / 12053
页数:7
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