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Expression of O6-methylguanine-DNA methyltransferase causes lomustine resistance in canine lymphoma cells

机译:O6-甲基鸟嘌呤-DNA甲基转移酶的表达引起犬淋巴瘤细胞洛莫司汀耐药

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摘要

The DNA repair protein O6-methylguanine-DNA methyltransferase (MGMT) causes resistance to nitrosoureas in various human cancers. In this study, we analyzed the correlation between canine lymphomas and MGMT in vitro. Two of five canine lymphoma cell lines required higher concentrations of lomustine to inhibit cell growth by 50%, but their sensitivity to the drug increased when they were cultured with an MGMT inhibitor. Fluorometric oligonucleotide assay and real-time polymerase chain reaction of these cell lines revealed MGMT activity and high MGMT mRNA expression, respectively. We analyzed the methylation status of the CpG islands of the canine MGMT gene by the bisulfite-sequencing method. Unlike human cells, the canine lymphoma cell lines did not show significant correlation between methylation status and MGMT suppression levels. Our results suggest that in canine lymphoma MGMT activity may influence sensitivity to nitrosoureas; thus, inhibition of MGMT activity would benefit nitrosourea-resistant patients. Additional studies are necessary to elucidate the mechanism of regulation of MGMT expression.
机译:DNA修复蛋白O 6 -甲基鸟嘌呤-DNA甲基转移酶(MGMT)在多种人类癌症中引起对亚硝基脲的抗性。在这项研究中,我们分析了犬淋巴瘤与MGMT之间的相关性。五个犬淋巴瘤细胞系中的两个需要更高浓度的洛莫司汀以抑制细胞生长50%,但是当它们与MGMT抑制剂一起培养时,对药物的敏感性增加。这些细胞系的荧光寡核苷酸测定和实时聚合酶链反应分别显示了MGMT活性和高MGMT mRNA表达。我们通过亚硫酸氢盐测序方法分析了犬MGMT基因CpG岛的甲基化状态。与人类细胞不同,犬淋巴瘤细胞系在甲基化状态和MGMT抑制水平之间没有显示出显着的相关性。我们的结果表明,犬淋巴瘤中MGMT的活性可能会影响对亚硝基脲的敏感性。因此,抑制MGMT活性将使耐亚硝基脲的患者受益。需要更多的研究来阐明MGMT表达的调节机制。

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