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Triptolide downregulates human GD3 synthase (hST8Sia I) gene expression in SK-MEL-2 human melanoma cells

机译:雷公藤甲素下调SK-MEL-2人黑素瘤细胞中人GD3合酶(hST8Sia I)基因表达

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摘要

In this study, we have shown that gene expression of human GD3 synthase (hST8Sia I) is suppressed by triptolide (TPL) in human melanoma SK-MEL-2 cells. To elucidate the mechanism underlying the downregulation of hST8Sia I gene expression in TPL-treated SK-MEL-2 cells, we characterized the TPL-inducible promoter region within the hST8Sia I gene using luciferase constructs carrying 5'-deletions of the hST8Sia I promoter. Functional analysis of the 5'-flanking region of the hST8Sia I gene demonstrated that the -1146 to -646 region, which contains putative binding sites for transcription factors c-Ets-1, CREB, AP-1 and NF-κB, functions as the TPL-inducible promoter of hST8Sia I in SK-MEL-2 cells. Site-directed mutagenesis and ChIP analysis indicated that the NF-κB binding site at -731 to -722 is crucial for TPL-induced suppression of hST8Sia I in SK-MEL-2 cells. This suggests that TPL induces down-regulation of hST8Sia I gene expression through NF-κB activation in human melanoma cells.
机译:在这项研究中,我们已经表明雷公藤内酯醇(TPL)在人黑素瘤SK-MEL-2细胞中抑制了人GD3合酶(hST8Sia I)的基因表达。为了阐明在TPL处理的SK-MEL-2细胞中hST8Sia I基因表达下调的潜在机制,我们使用了带有hST8Sia I启动子5'缺失的荧光素酶构建体,对hST8Sia I基因内的TPL诱导型启动子区域进行了表征。对hST8Sia I基因5'侧翼区的功能分析表明,-1146至-646区含有假定的转录因子c-Ets-1,CREB,AP-1和NF-κB结合位点,其功能如下:在SK-MEL-2细胞中hST8Sia I的TPL诱导型启动子。定点诱变和ChIP分析表明,-731至-722处的NF-κB结合位点对TPL诱导的SK-MEL-2细胞中hST8Sia I的抑制至关重要。这表明TPL通过人黑素瘤细胞中的NF-κB激活诱导hST8Sia I基因表达下调。

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