Abstract

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.

Highlights

  • Nanosecond pulsed electric fields have been shown to cause cell apoptosis, and investigated as a potential application for cancer therapy [1]

  • Cell death caused by Nanosecond pulsed electric fields (nsPEF) occurred in a voltage- and pulse number-dependent fashion

  • We found that the nsPEFtreatment of the carcinogen-induced tumors had decreased expression of the apoptosis-protective proteins Bcl-xl and Bcl-2 as measured by immunohistochemistry, and the tumors had increased apoptosis as measured by TUNEL assay (Figures 5 B C and D)

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Summary

Introduction

Nanosecond pulsed electric fields (nsPEF) have been shown to cause cell apoptosis, and investigated as a potential application for cancer therapy [1]. Nanopulses influence cell activity by a number of means, notably increasing plasma membrane and intracellular membrane permeability and causing alterations of phosphatidylserine distribution (demonstrated by Annexin V binding). Nanopulses induce intracellular events such as calcium release, caspase activation, and release of cytochrome C into the cytoplasm [1,3,4,5,6,7,8]. Nanopulses can induce apoptosis in human cancer cells [3]. Shorter duration nsPEF of up to 20 KV/cm can deliver energy to cells without increasing the temperature of exposed cells for pulse repetition rates of 1 MHz or less [10]

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