志贺宁通过增强口腔癌细胞的细胞内活性氧生成和 DNA 损伤来刺激线粒体介导的细胞凋亡

IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Stuti Biswal, Munmun Panda, Bijesh Kumar Biswal
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引用次数: 0

摘要

与克服化疗耐药性的传统化疗药物相比,植物疗法为包括口腔癌在内的各种癌症的治疗提供了一种副作用较小的新见解。Shikonin(Shk)是一种天然生物活性生物碱,存在于Lithospermum erythrorhizon植物的根部。它对各种癌症具有强大的细胞毒活性。我们的研究揭示了 Shk 对 SCC9 和 H357 口腔癌细胞系的释放时间和抗癌潜力。我们通过 MTT 和形态学检测、菌落和瘤球形成检测、AO/EtBr 和 DAPI 染色、Annexin V-FITC/PI 染色、活性氧(ROS)检测和线粒体膜电位(MMP)测量、彗星检测、qRT-PCR 和 Western 印迹分析,研究了 Shk 在口腔癌细胞中的抗增殖、抗移行、细胞周期阻滞和促进凋亡活性。我们还通过对接、CD 光谱和 EtBr 置换实验检测了 DNA 与 Shk 的相互作用。结果发现,Shk 能以时间和浓度依赖性的方式降低 SCC9 和 H357 细胞的活力、增殖和致瘤性。对 SCC9 和 H357 细胞的半数最大抑制浓度(IC50)分别为 0.5 µM 和 1.25 µM。它通过提高 ROS 导致 MMP 耗竭和 DNA 损伤,并使细胞停滞在 G2/M 和 G2/S 期,从而过度表达促凋亡的 Bax 和 caspase 3,促进细胞凋亡。Shk 的抗移行活性是通过分析上皮-间质转化标志物(如 E-cadherin、ZO-1、N-cadherin 和波形蛋白)的表达来实现的。这些总体结果表明,Shk 在体外和体内对口腔癌细胞株都有很强的抗癌活性。因此,它可能是治疗口腔癌的一种很好的药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Shikonin Stimulates Mitochondria-Mediated Apoptosis by Enhancing Intracellular Reactive Oxygen Species Production and DNA Damage in Oral Cancer Cells.

Phytotherapy has rendered a new insight towards the treatment of various cancers, including oral cancer with fewer side effects, over the traditional chemotherapeutic drugs to overcome chemoresistance. Shikonin (Shk) is a natural biologically active alkaloid found in the Lithospermum erythrorhizon plant's root. It has potent cytotoxic activities against various cancers. Our study revealed the release time and anticancer potential of Shk on the SCC9 and H357 oral cancer cell lines. We investigated the antiproliferative, antimigratory, cell cycle arresting and apoptosis promoting activity of Shk in oral cancer cells by performing MTT and morphological assay, colony, and tumor sphere formation assay, AO/EtBr and DAPI staining, Annexin V-FITC/PI staining, assay for reactive oxygen species (ROS) and mitochondrial membrane potential (MMP) measurement, comet assay, qRT-PCR, and western blot analysis. We also checked the interaction of DNA and Shk by docking and CD spectroscopy and EtBr displacement assay. As a result, we found that Shk reduced the viability, proliferation, and tumorigenicity of SCC9 and H357 cells in a time and concentration-dependent manner. We obtained half-maximal inhibitory concentration (IC50) at 0.5 µM for SCC9 and 1.25 µM for H357. It promotes apoptosis via overexpressing proapoptotic Bax and caspase 3 via enhancing ROS that leads to MMP depletion and DNA damage and arrests cells at the G2/M & G2/S phase. The antimigratory activity of Shk was performed by analyzing the expression of markers of epithelial-mesenchymal transition like E-cadherin, ZO-1, N-cadherin, and vimentin. These overall results recommended that Shk shows potent anticancer activity against oral cancer cell lines in both in vitro and ex vivo conditions. So, it could be an excellent agent for the treatment of oral cancer.

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来源期刊
Journal of cellular biochemistry
Journal of cellular biochemistry 生物-生化与分子生物学
CiteScore
9.90
自引率
0.00%
发文量
164
审稿时长
1 months
期刊介绍: The Journal of Cellular Biochemistry publishes descriptions of original research in which complex cellular, pathogenic, clinical, or animal model systems are studied by biochemical, molecular, genetic, epigenetic or quantitative ultrastructural approaches. Submission of papers reporting genomic, proteomic, bioinformatics and systems biology approaches to identify and characterize parameters of biological control in a cellular context are encouraged. The areas covered include, but are not restricted to, conditions, agents, regulatory networks, or differentiation states that influence structure, cell cycle & growth control, structure-function relationships.
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