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Stearoyl-CoA Desaturase-1 Enzyme Inhibition by Grape Skin Extracts Affects Membrane Fluidity in Human Colon Cancer Cell Lines

机译:葡萄皮提取物对硬脂酰-CoA去饱和酶-1酶的抑制作用影响人结肠癌细胞系中的膜流动性。

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摘要

The polyphenolic compounds present in grape extracts have chemopreventive and anticancer properties. Here, we studied the ability of two grape skin extracts (GSEs), Autumn Royal and Egnatia, to influence the cell motility and membrane fluidity regulated by the enzyme Stearoyl-CoA desaturase-1 (SCD1) which increases with the cancer aggressiveness. Caco2 and SW480 human colon cancer cell lines were treated with increasing concentrations of GSEs to evaluate cell proliferation and motility. SCD1 levels were evaluated in both treated cell lines, by membrane lipidomic analysis conducted by gas chromatography. The expression levels of SCD1 and other factors involved in the reorganization of the cytoskeleton and focal adhesions were assessed by Real-time PCR, Western Blotting, and Immunofluorescence staining. High-performance liquid chromatography (HPLC) analyses were performed to determine the phenolic composition in the GSEs, finding them more expressed in Autumn Royal than in Egnatia. Both treatments reduced the levels of SCD1, phospho-Rac1/Cdc42/Rac1/Cdc42 ratio, Cofilin, Vimentin, and phospho-Paxillin especially in Caco2 compared to SW480, showing a different behavior of the two cell lines to these natural compounds. Our findings show that GSEs block the cell migration and membrane fluidity through a new mechanism of action involving structural cellular components.
机译:葡萄提取物中存在的多酚化合物具有化学预防和抗癌特性。在这里,我们研究了两种葡萄皮提取物(GSE),即Royal Royal和Egnatia,影响由Stearoyl-CoA desaturase-1(SCD1)酶调节的细胞运动性和膜流动性的能力,该酶随癌症的侵袭性增加。用递增浓度的GSE处理Caco2和SW480人结肠癌细胞系,以评估细胞增殖和运动能力。通过气相色谱法进行膜脂质组分析,评估了两种处理过的细胞系中的SCD1水平。通过实时PCR,蛋白质印迹和免疫荧光染色评估了SCD1和其他参与细胞骨架重组和黏着斑粘附的因子的表达水平。进行了高效液相色谱(HPLC)分析,以确定GSE中的酚类成分,发现它们在Royal Royal中比在Egnatia中表达更多。与SW480相比,两种处理均降低了CCD2中的SCD1,磷酸-Rac1 / Cdc42 / Rac1 / Cdc42比率,Cofilin,波形蛋白和磷酸-Paxillin的水平,尤其是在Caco2中,显示了两种细胞系与这些天然化合物的行为不同。我们的发现表明,GSE通过涉及结构性细胞成分的新作用机制来阻止细胞迁移和膜流动性。

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