首页> 外文期刊>Tumour biology : >Upregulation of ZNRD1 enhances cisplatin resistance in human esophageal cancer cells by regulation of ERCC1 and Bcl-2.
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Upregulation of ZNRD1 enhances cisplatin resistance in human esophageal cancer cells by regulation of ERCC1 and Bcl-2.

机译:ZNRD1的上调通过调节ERCC1和Bcl-2增强人食道癌细胞中的顺铂耐药性。

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摘要

BACKGROUND/AIMS: The precise mechanism of the zinc ribbon domain-containing-1 (ZNRD1) gene on cisplatin resistance remains unclear. The aim of this study is to identify the gene expression profile and explore the role of these genes in ZNRD1-induced cisplatin resistance in esophageal cancer cells. METHODS: An expression vector with ZNRD1 was transfected into the EC109 cells, and then cDNA microarray analysis was performed to identify the gene expression profile. The sensitivity of transfected EC109 cells to cisplatin was evaluated using the MTT assay. RT-PCR and Western blots were performed to validate the differential expression of genes identified by cDNA microarray analysis. RESULTS: We identified 16 genes with significantly different expression levels between the transfected and control cells. The tolerance of EC109 cells to cisplatin was significantly enhanced by the upregulation of ZNRD1. Furthermore, the expression of excision repair cross-complementing-1 (ERCC1) and B-cell lymphoma-2 (Bcl-2) was significantly upregulated. CONCLUSION: The ZNRD1 gene might be involved in the cisplatin resistance of EC109 cells by regulating the expression of ERCC1 and Bcl-2.
机译:背景/目的:含锌带域-1(ZNRD1)基因对顺铂耐药的确切机制仍不清楚。这项研究的目的是确定基因表达谱,并探讨这些基因在食管癌细胞中由ZNRD1诱导的顺铂耐药性中的作用。方法:将带有ZNRD1的表达载体转染到EC109细胞中,然后进行cDNA微阵列分析以鉴定基因表达谱。使用MTT测定法评估转染的EC109细胞对顺铂的敏感性。进行RT-PCR和蛋白质印迹以验证通过cDNA微阵列分析鉴定的基因的差异表达。结果:我们确定了16个基因,它们在转染细胞和对照细胞之间的表达水平明显不同。 ZNRD1的上调显着增强了EC109细胞对顺铂的耐受性。此外,切除修复交叉互补1(ERCC1)和B细胞淋巴瘤2(Bcl-2)的表达明显上调。结论:ZNRD1基因可能通过调控ERCC1和Bcl-2的表达参与EC109细胞的顺铂耐药性。

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