A New Drug-Free Cancer Therapy Using Ultraviolet Pulsed Irradiation. PDT (PhotoDynamic Therapy) to PPT (Pulsed Photon Therapy).

Johbu Itoh, Yoshiko Itoh
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Abstract

Background: Pulsed ultraviolet (UV) irradiation can be used to generate a broad UV-C spectrum. The pulsing nature of such a spectrum helps increase the damage to cancer cells, leading to their injury and death. In contrast, non-tumor cells repair the damage and survive the same pulsed UV irradiation energy. Herein, we describe the development of a pulsed UV irradiation method for cancer cell dysfunction that irradiates cells with pulsed light by generating tremendous instantaneous UV energy-tens of thousands of times greater than that generated by UV lamps-to cause specific cell injury and dysfunction of cancer cells.

Methods: A newly developed pulsed ultraviolet irradiation device was used. Features of the device used in this study. This device employs a quartz discharge xenon lamp. Cultured tumor cells and non-tumor cells were irradiated with pulsed light at different irradiation doses, and their reactions were observed using optical, electron, and laser microscopes.

Results: Cancer cells have more FAS (CD95) receptor domains than non-cancer cells, and pulsed UV irradiation stimulates the production of reactive oxygen species (ROS) and OH, which exceeds the oxidative stress removal function, resulting in cell injury and death. That is, at low UV doses, only cancer cells underwent cell death, whereas non-cancer cells did not. The pulsed UV irradiation technique directly destroys cancer cells and minimizes the number of residual cancer cells while allowing minimum invasion into non-tumor cells, thereby improving their survival. This suggests the possibility of activating the host's local immune response to eliminate residual cancer cells.

Conclusions: A newly developed pulsed UV radiation system shows potential for use in the development of a drug-free cancer treatment system that selectively kills tumor cells by irradiating them with high-intensity pulsed UV rays over a broad UV-C range of 230-280 nm.

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一种新的无药物治疗癌症的紫外线脉冲照射。PDT(光动力疗法)到PPT(脉冲光子疗法)。
背景:脉冲紫外线(UV)照射可以产生广泛的UV- c光谱。这种光谱的脉冲性质有助于增加对癌细胞的伤害,导致它们受伤和死亡。相反,非肿瘤细胞修复损伤并在相同的脉冲紫外线照射能量下存活。在此,我们描述了一种用于癌细胞功能障碍的脉冲紫外线照射方法的发展,该方法通过产生巨大的瞬时紫外线能量(比紫外线灯产生的能量大数万倍)来照射细胞,以引起癌细胞的特定细胞损伤和功能障碍。方法:采用新研制的脉冲紫外线照射装置。本研究中使用的设备的特点。这个装置采用石英放电氙灯。用不同照射剂量的脉冲光照射培养的肿瘤细胞和非肿瘤细胞,用光学显微镜、电子显微镜和激光显微镜观察它们的反应。结果:癌细胞比非癌细胞具有更多的FAS (CD95)受体结构域,脉冲紫外线照射刺激活性氧(ROS)和OH的产生,超出氧化应激去除功能,导致细胞损伤和死亡。也就是说,在低紫外线剂量下,只有癌细胞发生细胞死亡,而非癌细胞则没有。脉冲紫外线照射技术直接破坏癌细胞,使残留癌细胞的数量降到最低,同时使对非肿瘤细胞的侵袭降到最低,从而提高非肿瘤细胞的存活率。这表明有可能激活宿主的局部免疫反应来消除残留的癌细胞。结论:一种新开发的脉冲紫外线辐射系统显示出在开发无药物癌症治疗系统中使用的潜力,该系统通过在230-280 nm宽UV- c范围内照射高强度脉冲紫外线,选择性地杀死肿瘤细胞。
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