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Stimulus-induced expression of the ABCG2 multidrug transporter in HepG2 hepatocarcinoma model cells involves the ERK1/2 cascade and alternative promoters

机译:在HepG2肝癌模型细胞中刺激诱导的ABCG2多药转运蛋白表达涉及ERK1 / 2级联和替代启动子

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摘要

The ATP-binding cassette G subfamily member ABCG2 protein is involved in drug resistance of various types of cancer including hepatocellular carcinoma (HCC). The transcriptional regulation of the ABCG2 gene was shown to depend on various transcription factors, and three alternative promoters were described. Here we aimed to decipher the role of hepatocyte growth factor (HGF) and the related kinase cascades on the expression of ABCG2 and the role of the different promoters in this process in the HepG2 human HCC cell line. We observed that HGF treatment increased the amount of ABCG2 on the cell surface in parallel with an increased ABCG2 transcription. ABCG2 mRNA expression was also increased by EGF, oxidative stress or activation of the aryl hydrocarbon receptor, while decreased by TGFb. Treatment with U0126, a specific inhibitor of the ERK1/2 cascade, prevented the HGF and the oxidative stress induced ABCG2 upregulation. We also show that the regulation of ABCG2 by various modulators involve specific alternative promoters. In conclusion, we demonstrate a unique role of the ERK1/2 cascade on ABCG2 modulation in HepG2, and the differential use of the alternative ABCG2 promoters in this cell line. This study reveals the molecular participants of ABCG2 overexpression as new potential treatment targets in HCC.
机译:ATP结合盒G亚家族成员ABCG2蛋白与包括肝细胞癌(HCC)在内的各种癌症的耐药性有关。已显示ABCG2基因的转录调控取决于各种转录因子,并描述了三个替代启动子。在这里,我们旨在破译肝细胞生长因子(HGF)和相关激酶级联在ABCG2表达上的作用以及不同启动子在HepG2人类HCC细胞系中的作用。我们观察到,HGF处理与增加的ABCG2转录平行地增加了细胞表面上ABCG2的量。 EGF,氧化应激或芳烃受体的活化也增加了ABCG2 mRNA的表达,而TGFb降低了ABCG2 mRNA的表达。用U0126(一种ERK1 / 2级联的特异性抑制剂)进行的治疗可防止HGF和氧化应激诱导的ABCG2上调。我们还表明,各种调节剂对ABCG2的调节涉及特定的替代启动子。总之,我们证明了ERK1 / 2级联对HepG2中ABCG2调控的独特作用,以及在该细胞系中不同ABCG2启动子的不同用途。这项研究揭示了ABCG2过表达的分子参与者是HCC中新的潜在治疗靶标。

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