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首页> 外文期刊>Cancer Cell International >Augmented expression of cardiac ankyrin repeat protein is induced by pemetrexed and a possible marker for the pemetrexed resistance in mesothelioma cells
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Augmented expression of cardiac ankyrin repeat protein is induced by pemetrexed and a possible marker for the pemetrexed resistance in mesothelioma cells

机译:培美曲塞可诱导心脏锚蛋白重复蛋白的表达增强,并且可能是间皮瘤细胞中培美曲塞耐药的标志物

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Pemetrexed (PEM) is an anti-cancer agent targeting DNA and RNA synthesis, and clinically in use for mesothelioma and non-small cell lung carcinoma. A mechanism of resistance to PEM is associated with elevated activities of several enzymes involved in nucleic acid metabolism. We established two kinds of PEM-resistant mesothelioma cells which did not show any increase of the relevant enzyme activities. We screened genes enhanced in the PEM-resistant cells with a microarray analysis and confirmed the expression levels with Western blot analysis. A possible involvement of the candidates in the PEM-resistance was examined with a WST assay after knocking down the expression with si-RNA. We also analyzed a mechanism of the up-regulated expression with agents influencing AMP-activated protein kinase (AMPK) and p53. We found that expression of cardiac ankyrin repeat protein (CARP) was elevated in the PEM-resistant cells with a microarray and Western blot analysis. Down-regulation of CARP expression with si-RNA did not however influence the PEM resistance. Parent and PEM-resistant cells treated with PEM increased expression of CARP, AMPK, p53 and histone H2AX. The CARP up-regulation was however irrelevant to the p53 genotypes and not induced by an AMPK activator. Augmented p53 levels with nutlin-3a, an inhibitor for p53 degradation, and DNA damages were not always associated with the enhanced CARP expression. These data collectively suggest that up-regulated CARP expression is a potential marker for development of PEM-resistance in mesothelioma and that the PEM-mediated enhanced expression is not directly linked with immediate cellular responses to PEM.
机译:培美曲塞(PEM)是靶向DNA和RNA合成的抗癌药,临床上用于间皮瘤和非小细胞肺癌。对PEM有抗性的机制与参与核酸代谢的几种酶的活性升高有关。我们建立了两种对PEM耐药的间皮瘤细胞,它们均未显示相关酶活性的任何增加。我们通过微阵列分析筛选了在PEM耐药细胞中增强的基因,并通过Western印迹分析确认了表达水平。在用si-RNA敲除表达后,通过WST分析检查了候选物可能参与PEM抗性。我们还分析了影响AMP激活的蛋白激酶(AMPK)和p53的药物表达上调的机制。我们发现,通过微阵列和Western印迹分析,心脏锚蛋白重复蛋白(CARP)的表达在PEM耐药细胞中升高。 si-RNA对CARP表达的下调并不影响PEM耐药性。用PEM处理的亲本和PEM耐药细胞会增加CARP,AMPK,p53和组蛋白H2AX的表达。然而,CARP的上调与p53基因型无关,并且不是由AMPK激活剂诱导的。使用坚果蛋白3a(p53降解抑制剂和DNA损伤)增强的p53水平并不总是与CARP表达增强有关。这些数据共同表明,上调的CARP表达是间皮瘤中PEM耐药性发展的潜在标志,并且PEM介导的增强表达与对PEM的直接细胞反应没有直接联系。

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