Potentiation of cytotoxicity of adriamycin on human ovarian carcinoma cell line 3AO by low-level ultrasound

被引:48
|
作者
Yu, T
Wang, ZB
Jiang, S
机构
[1] Chongqing Med Univ, Inst Ultrasound Engn Med, Chongqing 400016, Peoples R China
[2] Shandong Med Univ, Affiliated Hosp, Jinan 250012, Peoples R China
关键词
ovarian carcinoma; ultrasound; adriamycin; cytotoxicity;
D O I
10.1016/S0041-624X(01)00051-8
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
The aim of this study was to determine whether the ultrasound, with a dosage that did not lead to acute and delayed inhibition, could potentiate the cytotoxicity of adriamycin to human ovarian carcinoma cell line 3AO in vitro. Drug sensitivity was analyzed by clonogenic assay, cells were treated by adriamycin singly in group ADM (control), adriamycin prior to ultrasound exposure in group ADM + US, and ultrasound irradiation prior to adriamycin administration in group US + ADM. The intracellular drug accumulation in each group was determined by fluorometry. The results were: (1) the values of IC50 were 0.0083, <0.001 and 0.0065 mug/ mi in group ADM, ADM + US and US + ADM respectively; the clone surviving rate in group ADM + US and in group US + ADM were decreased (P < 0.001, P < 0.01), compared with control; the surviving rate in group ADM + US was lower than that in group US + ADM (P < 0.01). (2) The intracellular drug accumulations in group ADM + US were promoted (P < 0.01) and not increased significantly in group US + ADM (P > 0.05). These suggested that the low-level ultrasound could enhance the cytotoxicity of adriamycin to human ovarian carcinoma cells and promoted intracellular drug contents played the leading role. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:307 / 309
页数:3
相关论文
共 17 条
  • [1] Reversal of adriamycin resistance in ovarian carcinoma cell line by combination of verapamil and low-level ultrasound
    Yu, TH
    Hu, K
    Bai, J
    Wang, ZB
    ULTRASONICS SONOCHEMISTRY, 2003, 10 (01) : 37 - 40
  • [2] Effects of Dexamethasone on glucocorticoid receptor expression in a human ovarian carcinoma cell line 3AO
    Xu, MJ
    Song, LN
    Wang, ZM
    CHINESE MEDICAL JOURNAL, 2003, 116 (03) : 392 - 395
  • [4] The use of models in "target" theory to evaluate the survival curves of human ovarian carcinoma cell line exposure to adriamycin combined with ultrasound
    Yu, TY
    Xiong, ZA
    Chen, SR
    Tu, G
    ULTRASONICS SONOCHEMISTRY, 2005, 12 (05) : 345 - 348
  • [5] Efficacy of combined therapy with paclitaxel and low-level ultrasound in human chronic myelogenous leukemia cell line K562
    Yang, Shuang
    Wang, Pan
    Wang, Xiaobing
    Zhang, Kun
    Zhang, Xing
    Liu, Quanhong
    JOURNAL OF DRUG TARGETING, 2013, 21 (09) : 874 - 884
  • [6] HPMA copolymer bound adriamycin overcomes MDR1 gene encoded resistance in a human ovarian carcinoma cell line
    Minko, T
    Kopeckova, P
    Pozharov, V
    Kopecek, J
    JOURNAL OF CONTROLLED RELEASE, 1998, 54 (02) : 223 - 233
  • [7] Chronic exposure to HPMA copolymer-bound adriamycin does not induce multidrug resistance in a human ovarian carcinoma cell line
    Minko, T
    Kopecková, P
    Kopecek, J
    JOURNAL OF CONTROLLED RELEASE, 1999, 59 (02) : 133 - 148
  • [8] Biological effects of ultrasound exposure on adriamycin-resistant and cisplatin-resistant human ovarian carcinoma cell lines in vitro
    Yu, TH
    Bai, J
    Hu, K
    Wang, ZB
    ULTRASONICS SONOCHEMISTRY, 2004, 11 (02) : 89 - 94
  • [9] HPMA copolymer-anticancer drug-OV-TL16 antibody conjugates.: 3.: The effect of free and polymer-bound Adriamycin on the expression of some genes in the OVCAR-3 human ovarian carcinoma cell line
    Kunath, K
    Kopecková, P
    Minko, T
    Kopecek, J
    EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2000, 49 (01) : 11 - 15
  • [10] Electrochemical monitoring of anticancer compounds on the human ovarian carcinoma cell line A2780 and its adriamycin- and cisplatin-resistant variants
    Woolley, DE
    Tetlow, LC
    Adlam, DJ
    Gearey, D
    Eden, RD
    Ward, TH
    Allen, TD
    EXPERIMENTAL CELL RESEARCH, 2002, 273 (01) : 65 - 72