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首页> 外文期刊>Nutrition and Cancer: An International Journal >Japanese black vinegar 'izumi' inhibits the proliferation of human squamous cell carcinoma cells via necroptosis
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Japanese black vinegar 'izumi' inhibits the proliferation of human squamous cell carcinoma cells via necroptosis

机译:日本黑醋“泉”通过坏死病抑制人鳞状细胞癌细胞的增殖

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Kurozu (Japanese black vinegar), a traditional product made from unpolished rice, contains beneficial organic materials and minerals. Improved manufacturing processes yielded a new vinegar, Izumi, that contains large amounts of these constituents. Because the antioxidative effects of Kurozu are well understood, we examined Izumi for its anticancer activity against the human squamous cell carcinoma (SCC) cell line HSC-5. HSC-5 cells were treated with Izumi or ordinary grain vinegar adjusted to 4.2% acidicity. MTT assay and the trypan blue dye exclusion test showed that Izumi significantly inhibited the proliferation of HSC-5 cells compared to ordinary grain vinegar. Propidium iodide (PI) flow cytometry and annexin V/PI staining revealed that among cells treated or untreated with Izumi or ordinary grain vinegar there was no difference in the number of apoptotic cells. A new form of necrosis, programmed necrosis or necroptosis, has been proposed. It is mediated by receptor-interacting serine-threonine kinase 3 (RIPK3), key signaling molecule, and results in the release of cellular danger-associated molecular patterns (DAMPs). When HSC-5 cells were treated with Izumi, the cellular level of RIPK3 protein and the amount of high-mobility group protein B1, one of the DAMPs, released into culture media were remarkably increased. These findings indicate that Izumi inhibits the proliferation of human SCC cells via programmed necrosis (necroptosis).
机译:黑米是一种由糙米制成的传统产品,含有有益的有机物质和矿物质。生产工艺的改进产生了一种新的醋Izumi,其中含有大量的这些成分。因为黑醋栗的抗氧化作用是众所周知的,所以我们检查了Izumi对人类鳞状细胞癌(SCC)细胞系HSC-5的抗癌活性。将HSC-5细胞用Izumi或调节至4.2%酸性的普通谷物醋处理。 MTT分析和锥虫蓝染料排除试验表明,与普通谷物醋相比,Izumi显着抑制了HSC-5细胞的增殖。碘化丙啶(PI)流式细胞术和膜联蛋白V / PI染色显示,在用Izumi或普通谷物醋处理或未处理的细胞中,凋亡细胞的数量没有差异。已经提出了一种新形式的坏死,程序性坏死或坏死性坏死。它是由关键信号分子与受体相互作用的丝氨酸-苏氨酸激酶3(RIPK3)介导的,并导致释放与细胞危险相关的分子模式(DAMPs)。用Izumi处理HSC-5细胞时,释放到培养基中的RIPK3蛋白的细胞水平和DAMPs之一的高迁移率基团蛋白B1的量显着增加。这些发现表明,Izumi通过程序性坏死(坏死性坏死)抑制人SCC细胞的增殖。

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