Zhai Bao-jin, Wu Feng, Shao Ze-yong, Hu Kai, Zhao Chun-liang, Wang Zhi-biao
The Center for Tumor Therapy, 2nd Affiliated Hospital, Chongqing University of Medical Science, Chongqing 400010, China.
Zhonghua Gan Zang Bing Za Zhi. 2004 Feb;12(2):95-8.
To establish human hepatocellular carcinoma multidrug-resistance cell line (HepG2/ADM) and to determine the effect of low-frequency pulse ultrasound (US) on MDR cells and investigate its mechanism.
Using gradual increase of adriamycin (ADM) concentrations in culture, an adriamycin-resistant human hepatocellular carcinoma cell sub line (HepG2/ADM) was established in vitro. HepG2/ADM cells were cultured in vitro and randomly divided into 4 groups: the control group (HepG2/ADM only), the group ADM by 1.0 mug/ml adriamycin for 1 h, the group US by low-frequency pulse ultrasound for 10 min, and the group US by low-frequency pulse ultrasound and treated with adriamycin simultaneously at same time. A sonication at a frequency of 0.8 MHz, was delivered with an intensity level of 0.5W/cm2, with continuous exposure of 10 min was applied. The ability of US to induce the apoptosis of MDR was evaluated by analyses of fluorescence microscopy, DNA fragmentation assay and flow cytometry assay.
HepG2/Adm was resistant to many anti-tumor agents, and its IC50 of ADM was 26 times higher than that of parent cell line HepG2. Significant over expressions of P-gp, MRP, LRP and GSTs were detected. HepG2/ADM cells radiated by US had the typical characteristics of apoptosis. Compared with the control group (HepG2/ADM, 3.47%); the apoptosis rates were higher in US (12.23%). The therapeutic alliance of US with ADM for MDR cells, have a significant change in the ratio of apoptosis (18.81%, t=1.46 to 5.36, P<0.01).
HepG2/ADM could have the biological characteristics of human multidrug-resistance cell line. The US sonication of 0.8 MHz could induce apoptosis of HepG2/ADM cell in vitro, and could act synergistically with Adriamycin.
建立人肝癌多药耐药细胞系(HepG2/ADM),探讨低频脉冲超声(US)对多药耐药细胞的作用及其机制。
通过在培养过程中逐渐增加阿霉素(ADM)浓度,体外建立阿霉素耐药人肝癌细胞亚系(HepG2/ADM)。将HepG2/ADM细胞体外培养并随机分为4组:对照组(仅HepG2/ADM)、1.0μg/ml阿霉素处理1小时组、低频脉冲超声处理10分钟组、低频脉冲超声处理并同时给予阿霉素组。采用频率为0.8MHz、强度为0.5W/cm²、连续照射10分钟的超声处理。通过荧光显微镜分析、DNA片段化检测和流式细胞术检测评估超声诱导多药耐药细胞凋亡的能力。
HepG2/Adm对多种抗肿瘤药物耐药,其阿霉素的IC50比亲本细胞系HepG2高26倍。检测到P-糖蛋白、多药耐药相关蛋白、肺耐药蛋白和谷胱甘肽S-转移酶的显著过表达。超声照射的HepG2/ADM细胞具有典型的凋亡特征。与对照组(HepG2/ADM,3.47%)相比,超声组的凋亡率更高(12.23%)。超声与阿霉素联合治疗多药耐药细胞,凋亡率有显著变化(18.81%,t = 1.46至5.36,P < 0.01)。
HepG2/ADM具有人多药耐药细胞系的生物学特性。0.8MHz的超声照射可在体外诱导HepG2/ADM细胞凋亡,并可与阿霉素协同作用。