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Expression of asparagine synthetase predicts in vitro response to l-asparaginase in canine lymphoid cell lines

机译:天冬酰胺合成酶的表达预测犬淋巴样细胞系中对l-天冬酰胺酶的体外反应

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摘要

l-asparaginase (L-asp), a bacterial enzyme that depletes extracellular asparagine, is used to treat acute lymphoblastic leukemia in humans and a variety of aggressive lymphoid malignancies in dogs. Resistance to this drug is an important cause of treatment failure in both species. Using canine lymphoid cell lines, we found that L-asp sensitivity is strongly negatively correlated with the level of methylation of the asparagine synthetase (ASNS) promoter. Selection for in vitro resistance was accompanied by increased ASNS promoter methylation and decreased ASNS mRNA expression. In addition, treatment with the hypomethylating agent 5-azacytidine increased resistance to L-asp. ASNS methylation and expression is not predictive of overall survival or progression-free survival in canine lymphoma patients treated with L-asp. Our data suggest that ASNS is an important factor in mediating the in vitro response of canine lymphoid cells to L-asp; however, resistance mechanisms may be more complex in dogs treated clinically with L-asp, potentially due to concurrent treatments.
机译:l-天冬酰胺酶(L-asp)是一种消耗细胞外天冬酰胺的细菌酶,用于治疗人的急性淋巴细胞白血病和狗的多种侵袭性淋巴恶性肿瘤。对这两种药物的耐药性是两个物种治疗失败的重要原因。使用犬淋巴样细胞系,我们发现L-asp敏感性与天冬酰胺合成酶(ASNS)启动子的甲基化水平强烈负相关。选择体外抗性伴随着增加的ASNS启动子甲基化和降低的ASNS mRNA表达。另外,用次甲基化剂5-氮杂胞苷处理增加了对L-asp的抗性。 ASNS甲基化和表达不能预测L-asp治疗的犬淋巴瘤患者的总生存或无进展生存。我们的数据表明,ASNS是介导犬淋巴样细胞对L-asp体外反应的重要因素。但是,在临床上用L-asp治疗的狗的耐药机制可能更复杂,这可能是由于同时进行治疗所致。

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