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Ozone at low concentrations does not affect motility and proliferation of cancer cells in vitro

机译:低浓度下的臭氧不会影响体外癌细胞的运动和增殖

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Exposure to low ozone concentrations is used in medicine as an adjuvant/complementary treatment for a variety of diseases. The therapeutic potential of low ozone concentrations relies on their capability to increase the nuclear translocation of the Nuclear factor erythroid 2-related factor 2 (Nrf2), thus inducing the transcription of Antioxidant Response Elements (ARE)-driven genes and, through a cascade of events, a general cytoprotective response. However, based on the controversial role of Nrf2 in cancer initiation, progression and resistance to therapies, possible negative effects of ozone therapy may be hypothesised in oncological patients. With the aim to elucidate the possible changes in morphology, migration capability and proliferation of cancer cells following mild ozone exposure, we performed wound healing experiments in vitro on HeLa cells treated with low ozone concentrations currently used in the clinical practice. By combining a multimodal microscopy approach (light and fluorescence microscopy, scanning electron microscopy, atomic force microscopy) with morphometric analyses, we demonstrated that, under our experimental conditions, exposure to low ozone concentrations does not alter cytomorphology, motility and proliferation features, thus supporting the notion that ozone therapy should not positively affect tumour cell growth and metastasis.
机译:暴露于低臭氧浓度的药物作为各种疾病的佐剂/互补治疗。低臭氧浓度的治疗潜力依赖于其增加核因子红外二态2相关因子2(NRF2)的核易位的能力,从而诱导抗氧化剂反应元素(A)的转录 - 驱动基因,并通过级联事件,一种一般的细胞保护反应。然而,基于NRF2在癌症起始,进展和对疗法抗性的争议作用,可能在肿瘤患者中假设臭氧治疗的可能对抗可能的负面影响。旨在阐明轻度臭氧暴露后癌细胞形态,迁移能力和增殖的可能变化,我们在临床实践中使用低臭氧浓度处理的Hela细胞体外进行伤口愈合实验。通过将多峰显微镜接近(光和荧光显微镜,扫描电子显微镜,原子力显微镜)与形态学分析相结合,我们证明,在我们的实验条件下,暴露于低臭氧浓度不会改变细胞形态,运动性和增殖特征,从而支撑臭氧治疗不应积极影响肿瘤细胞生长和转移的观念。

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