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首页> 外文期刊>Current cancer drug targets >Epigallocatechin-3-gallate Increases RXR gamma-mediated Pro-apoptotic and Anti-invasive Effects in Gastrointestinal Cancer Cell Lines
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Epigallocatechin-3-gallate Increases RXR gamma-mediated Pro-apoptotic and Anti-invasive Effects in Gastrointestinal Cancer Cell Lines

机译:Epigallocatechin-3-gallate增加胃肠道癌细胞系中RXRγ介导的促凋亡和抗侵袭作用

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摘要

Molecules with synergistic effects often enhance the benefits of cancer therapy. We observed that the major catechin of green tea, (-)-Epigallocatechin-3-gallate (EGCG), induced retinoid X receptor-gamma (RXR gamma) expression in the SK-Ch-A1 cholangiocarcinoma cell line and in two colon carcinoma cell lines (LoVo and the derivative multi-drug resistant LoVoMDR). On this basis, we analyzed the effects of EGCG in combination with an RXR gamma ligand, 6-OH-11-O-hydroxyphenantrene (IIF), or with a ligand of retinoic acid receptor, all-trans-retinoic acid (RA). IIF alone and in combination with EGCG activated the retinoic X response elements and induced the germ cell nuclear factor. In parallel, EGCG induced 67 kDa laminin receptor expression alone and in combination with IIF. We observed a synergistic growth inhibition with EGCG and IIF in combination at lower doses. These effects were accompanied by apoptosis activation through the mitochondrial pathway. Moreover, in LoVo cell line we observed an induction of Forkhead box O3 expression, another molecule involved in apoptosis activation. Finally, metalloproteinase activity and extracellular matrix metalloproteinase inducer (EMMPRIN) expression were inhibited and tumor cell invasion was strongly reduced in the SK-Ch-A1 cell line after treatment with EGCG and IIF. In conclusion, the use of specific RXR ligands in combination with catechins could open a new perspective in gastrointestinal tumor chemoprevention.
机译:具有协同作用的分子通常会增强癌症治疗的益处。我们观察到,绿茶的主要儿茶素(-)-Epigallocatechin-3-gallate(EGCG)在SK-Ch-A1胆管癌细胞系和两个结肠癌细胞中诱导类维生素X受体-γ(RXRγ)表达线(LoVo和派生的多药耐药性LoVoMDR)。在此基础上,我们分析了EGCG与RXRγ配体6-OH-11-O-羟基菲汀(IIF)或与视黄酸受体配体全反式视黄酸(RA)结合的效果。 IIF单独或与EGCG结合可激活视黄酸X反应元件并诱导生殖细胞核因子。同时,EGCG单独或与IIF一起诱导67 kDa层粘连蛋白受体表达。我们观察到在较低剂量下与EGCG和IIF联合产生的协同生长抑制作用。这些作用伴随着通过线粒体途径的凋亡激活。此外,在LoVo细胞系中,我们观察到前叉头O3表达的诱导,这是另一个参与凋亡激活的分子。最后,在用EGCG和IIF处理后,SK-Ch-A1细胞系中的金属蛋白酶活性和细胞外基质金属蛋白酶诱导剂(EMMPRIN)的表达被抑制并且肿瘤细胞的侵袭被大大减少。总之,将特定的RXR配体与儿茶素结合使用可以为胃肠道肿瘤的化学预防开辟新的前景。

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