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Triptolide-induced suppression of phospholipase D expression inhibits proliferation of MDA-MB-231 breast cancer cells

机译:雷公藤内酯醇对磷脂酶D表达的抑制作用抑制了MDA-MB-231乳腺癌细胞的增殖

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摘要

In spite of the importance of phospholipase D (PLD) in cell proliferation and tumorigenesis, little is known about the molecules regulating PLD expression. Thus, identification of small molecules inhibiting PLD expression would be an important advance for PLD-mediated physiology. We examined one such here, denoted "Triptolide", which was identified in a chemical screen for inhibitors of PLD expression using cell assay system based on measurement of PLD promoter activity. Triptolide significantly suppressed the expression of both PLD1 and PLD2 with sub-µM potency in MDA-MB-231 breast cancer cells as analyzed by promoter assay and RT-PCR. Moreover, triptolide abolished the protein level of PLD in a time and dose-dependent manner. Triptolide-induced PLD1 downregulation was also observed in all the cancer cells examined, suggesting a general phenomenon detected in various cancer cells. Decrease of PLD expression by triptolide suppressed both basal and PMA-induced PLD activity. In addition, triptolide inhibited activation of NFκB which increased PLD1 expression. Ultimately, downregulation of PLD by triptolide inhibited proliferation of breast cancer cells. Taken together, we demonstrate that triptolide suppresses the expression of PLD via inhibition of NFκB activation and then decreases cell proliferation.
机译:尽管磷脂酶D(PLD)在细胞增殖和肿瘤发生中很重要,但对调节PLD表达的分子知之甚少。因此,鉴定抑制PLD表达的小分子对于PLD介导的生理学将是重要的进展。我们在这里检查了一种称为“ Triptolide”的化合物,该化合物在化学筛选中使用细胞分析系统,基于对PLD启动子活性的测量,确定了PLD表达的抑制剂。雷公藤内酯醇通过启动子测定和RT-PCR分析显示,在MDA-MB-231乳腺癌细胞中以亚µM的效力显着抑制了PLD1和PLD2的表达。此外,雷公藤甲素以时间和剂量依赖性方式消除了PLD的蛋白质水平。在所有检查的癌细胞中也观察到雷公藤内酯醇诱导的PLD1下调,表明在各种癌细胞中检测到普遍现象。雷公藤甲素降低PLD表达可同时抑制基础和PMA诱导的PLD活性。此外,雷公藤甲素抑制NFκB的激活,从而增加PLD1表达。最终,雷公藤内酯对PLD的下调抑制了乳腺癌细胞的增殖。两者合计,我们证明雷公藤甲素通过抑制NFκB活化来抑制PLD的表达,然后降低细胞增殖。

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