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Cutaneous Papilloma and Squamous Cell Carcinoma Therapy Utilizing Nanosecond Pulsed Electric Fields (nsPEF)

机译:皮肤乳头状瘤和鳞状细胞癌治疗利用纳秒脉冲电场(nspEF)

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摘要

Nanosecond pulsed electric fields (nsPEF) induce apoptotic pathways in human cancer cells. The potential therapeutic effective of nsPEF has been reported in cell lines and in xenograft animal tumor model. The present study investigated the ability of nsPEF to cause cancer cell death in vivo using carcinogen-induced animal tumor model, and the pulse duration of nsPEF was only 7 and 14 nano second (ns). An nsPEF generator as a prototype medical device was used in our studies, which is capable of delivering 7–30 nanosecond pulses at various programmable amplitudes and frequencies. Seven cutaneous squamous cell carcinoma cell lines and five other types of cancer cell lines were used to detect the effect of nsPEF in vitro. Rate of cell death in these 12 different cancer cell lines was dependent on nsPEF voltage and pulse number. To examine the effect of nsPEF in vivo, carcinogen-induced cutaneous papillomas and squamous cell carcinomas in mice were exposed to nsPEF with three pulse numbers (50, 200, and 400 pulses), two nominal electric fields (40 KV/cm and 31 KV/cm), and two pulse durations (7 ns and 14 ns). Carcinogen-induced cutaneous papillomas and squamous carcinomas were eliminated efficiently using one treatment of nsPEF with 14 ns duration pulses (33/39 = 85%), and all remaining lesions were eliminated after a 2nd treatment (6/39 = 15%). 13.5% of carcinogen-induced tumors (5 of 37) were eliminated using 7 ns duration pulses after one treatment of nsPEF. Associated with tumor lysis, expression of the anti-apoptotic proteins Bcl-xl and Bcl-2 were markedly reduced and apoptosis increased (TUNEL assay) after nsPEF treatment. nsPEF efficiently causes cell death in vitro and removes papillomas and squamous cell carcinoma in vivo from skin of mice. nsPEF has the therapeutic potential to remove human squamous carcinoma.
机译:纳秒脉冲电场(nsPEF)诱导人癌细胞中的凋亡途径。已经在细胞系和异种移植动物肿瘤模型中报道了nsPEF的潜在治疗效果。本研究使用致癌物诱导的动物肿瘤模型研究了nsPEF在体内引起癌细胞死亡的能力,并且nsPEF的脉冲持续时间仅为7和14纳秒(ns)。在我们的研究中,使用了nsPEF发生器作为原型医疗设备,它能够以各种可编程的幅度和频率传送7–30纳秒的脉冲。七种皮肤鳞状细胞癌细胞系和五种其他类型的癌细胞系用于体外检测nsPEF的作用。在这12种不同的癌细胞系中,细胞死亡的速率取决于nsPEF电压和脉冲数。为了检查nsPEF的体内作用,将致癌剂诱发的皮肤乳头状瘤和鳞状细胞癌的小鼠暴露于nsPEF,其具有三个脉冲数(50、200和400脉冲),两个标称电场(40 KV / cm和31 KV) / cm)和两个脉冲持续时间(7 ns和14 ns)。使用nsPEF的一种治疗方法,以14 ns的持续时间脉冲有效地消除了由致癌物引起的皮肤乳头状瘤和鳞癌(33/39 = 85%),并在第二次治疗后消除了所有剩余的病变(6/39 = 15%)。一次nsPEF治疗后,使用7 ns持续时间脉冲消除了13.5%的致癌物诱导的肿瘤(37个中的5个)。 nsPEF处理后,与肿瘤溶解相关的抗凋亡蛋白Bcl-xl和Bcl-2的表达显着降低,凋亡增加(TUNEL分析)。 nsPEF在体外有效导致细胞死亡,并在体内从小鼠皮肤中去除乳头状瘤和鳞状细胞癌。 nsPEF具有去除人鳞癌的治疗潜力。

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