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毫米波治疗通过激活人骨肉瘤细胞中线粒体依赖性途径诱导细胞凋亡。

Millimeter wave treatment induces apoptosis via activation of the mitochondrial-dependent pathway in human osteosarcoma cells.

机构信息

Academy of Integrative Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou 350108, PR China.

出版信息

Int J Oncol. 2012 May;40(5):1543-52. doi: 10.3892/ijo.2012.1330. Epub 2012 Jan 12.

Abstract

Millimeter wave (MW) is an electromagnetic wave with a wavelength between 1 and 10 mm and a frequency of 30-300 GHz that causes multiple biological effects and has been used as a major component in physiotherapies for the clinical treatment of various types of diseases including cancers. However, the precise molecular mechanism of the anticancer activity of millimeter wave remains to be elucidated. In the present study, we investigated the cellular effects of the MW in the U-2OS human osteosarcoma cell line. Our results showed that MW induced cell morphological changes and reduced cell viability in a dose- and time-dependent manner suggesting that MW inhibited the growth of U-2OS cells as demonstrated. Hoechst 33258 staining and Annexin V/propidium iodide double staining exhibited the typical nuclear features of apoptosis and increased the proportion of apoptotic Annexin V-positive cells in a dose-dependent manner, respectively. In addition, MW treatment caused loss of plasma membrane asymmetry, release of cytochrome c, collapse of mitochondrial membrane potential, activation of caspase-9 and -3, and increase of the ratio of pro-apoptotic Bax to anti-apoptotic Bcl-2. Taken together, the results indicate that the U-2OS cell growth inhibitory activity of MW was due to mitochondrial-mediated apoptosis, which may partly explain the anticancer activity of millimeter wave treatment.

摘要

毫米波(MW)是一种波长在 1 到 10 毫米之间、频率在 30 到 300 千兆赫之间的电磁波,它会引起多种生物效应,并已被用作治疗各种类型疾病(包括癌症)的物理疗法的主要成分。然而,毫米波的抗癌活性的确切分子机制仍有待阐明。在本研究中,我们研究了 MW 在人骨肉瘤 U-2OS 细胞系中的细胞效应。我们的结果表明,MW 以剂量和时间依赖的方式诱导细胞形态变化和降低细胞活力,表明 MW 抑制了 U-2OS 细胞的生长,如所示。Hoechst 33258 染色和 Annexin V/碘化丙啶双重染色分别以剂量依赖性方式显示出凋亡的典型核特征,并增加了凋亡性 Annexin V 阳性细胞的比例。此外,MW 处理导致质膜不对称性丧失、细胞色素 c 释放、线粒体膜电位崩溃、半胱天冬酶-9 和 -3 的激活以及促凋亡 Bax 与抗凋亡 Bcl-2 的比例增加。总之,这些结果表明 MW 对 U-2OS 细胞生长的抑制活性是由于线粒体介导的凋亡,这可能部分解释了毫米波治疗的抗癌活性。

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