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Experimental Study of Ultrasound on MDR in a Human Tumor in Vivo
作者姓名:Baojin  Zhai  Liming  Chen  Yumian  Guo  ZhiHong  Wang  Feng  Wu  
作者单位:Baojin Zhai1 Liming Chen1 Yumian Guo1 ZhiHong Wang1 Feng Wu2 1 Department of Neurological Surgery,the Affiliated Hospital of The Medical Colege of Chinese People’sArmed Police Force,Tianjin 300162,China.2 Institute of Ultrasound and Engineering in Medicine,Chongqing University of Medical Science,Chongqing 400016,China.
基金项目:This work was supported by a grant from theNational Natural Science Foundation of China(No.30200060).
摘    要:OBJECTIVE To evaluate the potential efficacy of low-intensity ultrasound(US)in combination with anticancer drugs to reverse multidrug resistance(MDR)in nude mice. METHODS A total of 40 male and female athymic nude mice were inoculated subcutaneously with 5x106 HepG 2 /ADM and HepG 2 cells.Ultrasound with pulsed irradiation at an average intensity of 0.5 W/cm2 was given to the tumor area 10 min after administration of adriamycin(ADM).The tumor 3 dimensional diameters were measured by calipers before and after treatment, and the tumor growth indexes(TGI)calculated.RT-PCR was used to detect the gene levels of the HepG 2 /ADM cells.Immunohistochemical analyses for MDR proteins were conducted on the tumor tissues. RESULTS The ultrasonic treatment resulted in an average reduction in the tumor volume of 62%one month later.The relative mRNA levels of MDR1 and MRP were significantly different among the folowing 4 groups: untreated group as control,ADM treated;US treated;and ADM plus US treated.The mRNA levels of mdr1 and mrp were down-regulated in the US groups compared to those of the non-ultrasound groups by multiple com- parisons.The relative mRNA levels of lrp expression were not significantly changed.The results of immunohistochemistry indicated that tumor tissue from animals treated with US had remarkably low mdr1 and mrp expression. CONCLUSION The results showed that low-intensity US can effectively reduce the size of adriamycin-resistant human hepotacarcinoma in a nude mouse model,and support the efficacy of US to overcome multiple mechanisms of drug resistance.


Experimental Study of Ultrasound on MDR in a Human Tumor in Vivo
Baojin Zhai,Liming Chen,Yumian Guo,ZhiHong Wang,Feng Wu.Experimental Study of Ultrasound on MDR in a Human Tumor in Vivo[J].Chinese Journal of Clinical Oncology,2007,4(6).
Authors:Baojin Zhai  Liming Chen  Yumian Guo  ZhiHong Wang  Feng Wu
Abstract:OBJECTIVE To evaluate the potential efficacy of low-intensity ultrasound(US)in combination with anticancer drugs to reverse multidrug resistance(MDR)in nude mice. METHODS A total of 40 male and female athymic nude mice were inoculated subcutaneously with 5x106 HepG 2 /ADM and HepG 2 cells.Ultrasound with pulsed irradiation at an average intensity of 0.5 W/cm2 was given to the tumor area 10 min after administration of adriamycin(ADM).The tumor 3 dimensional diameters were measured by calipers before and after treatment, and the tumor growth indexes(TGI)calculated.RT-PCR was used to detect the gene levels of the HepG 2 /ADM cells.Immunohistochemical analyses for MDR proteins were conducted on the tumor tissues. RESULTS The ultrasonic treatment resulted in an average reduction in the tumor volume of 62%one month later.The relative mRNA levels of MDR1 and MRP were significantly different among the folowing 4 groups: untreated group as control,ADM treated;US treated;and ADM plus US treated.The mRNA levels of mdr1 and mrp were down-regulated in the US groups compared to those of the non-ultrasound groups by multiple com- parisons.The relative mRNA levels of lrp expression were not significantly changed.The results of immunohistochemistry indicated that tumor tissue from animals treated with US had remarkably low mdr1 and mrp expression. CONCLUSION The results showed that low-intensity US can effectively reduce the size of adriamycin-resistant human hepotacarcinoma in a nude mouse model,and support the efficacy of US to overcome multiple mechanisms of drug resistance.
Keywords:multidrug resistance (MDR)  HepG2/ADM  ultrasound (US)  nude mice  
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