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首页> 外文期刊>Technology in cancer research & treatment. >In vivo evidences of nanosecond pulsed electric fields for melanoma malignancy treatment on tumor-bearing BALB/c nude mice
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In vivo evidences of nanosecond pulsed electric fields for melanoma malignancy treatment on tumor-bearing BALB/c nude mice

机译:纳秒脉冲电场在荷瘤BALB / c裸鼠上治疗黑素瘤恶性肿瘤的体内证据

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摘要

In order to get in vivo evidences of nanosecond pulsed electric fields (nsPEF) for skin tumor treatment, tumor models in 10 female BALB/c nude mice were established by inoculating them with human melanoma cells A375. These mice were randomly divided into treated group (exposed to nsPEF with intensity of 20 kV/cm and duration of 300 ns) and control group equally. Five days post-nsPEF treatment, tumor growth in the treated group was effectively inhibited (P < 0.01 compared with that in control group), typical apoptotic characteristics (DNA damage and fragmentation) were observed by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL), and significant increases in Bax and decreases in Bcl-2, micro-vessel density (MVD), vascular endothelial growth factor (VEGF) and proliferating cell nuclear antigen (PCNA) were observed by immunohistochemistry (P < 0.01). These experimental results indicate that in vivo tumor growth can be effectively inhibited by nsPEF, which activate two targets, apoptosis initiation and angiogenesis inhibition.
机译:为了获得用于治疗皮肤肿瘤的纳秒脉冲电场(nsPEF)的体内证据,通过给人类黑素瘤细胞A375接种,在10只雌性BALB / c裸鼠中建立了肿瘤模型。将这些小鼠随机分为治疗组(暴露于强度为20 kV / cm,持续时间为300 ns的nsPEF)和对照组。 nsPEF治疗后5天,治疗组的肿瘤生长得到了有效抑制(与对照组相比,P <0.01),通过末端脱氧核苷酸转移酶dUTP缺口末端标记(TUNEL)观察到典型的凋亡特征(DNA损伤和断裂)。免疫组织化学观察到,Bax,Bcl-2,微血管密度(MVD),血管内皮生长因子(VEGF)和增殖细胞核抗原(PCNA)的表达显着升高(P <0.01)。这些实验结果表明,nsPEF可以有效地抑制体内肿瘤的生长,nsPEF可以激活两个靶标,即凋亡启动和血管生成抑制。

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