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The clinical relevance of the expression of several multidrug-resistant-related genes in patients with primary acute myeloid leukemia.

机译:原发性急性髓细胞性白血病患者中几种耐多药相关基因表达的临床意义。

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摘要

Multidrug resistance (MDR) is a complex phenomenon that includes the expression of many different genes regulating drug transport or metabolism, cellular repair or detoxification mechanisms. The co-expression of several genes could be at the basis of the resistant phenotype in vivo. In order to test a possible prognostic role of the expression and co-expression of several MDR-related genes (MDR1, topoisomerase IIalpha, topoisomerase IIbeta, MRP, GSTpi, LRP), 35 patients affected by acute myeloid leukemia (AML) were tested by RT-PCR assays. In our series, topoisomerase IIbeta was significantly co-expressed with MRP (p = 0.05), GSTpi (p = 0.017) and LRP (p = 0.005). GSTpi was co-expressed with LRP (p = 0.03) and MRP (p = 0.007); on the other hand, 53.8% of patients were LRP and MRP-positive (p = 0.02). The PCR-positivity did not differ according to biological/clinical characteristics of patients, including age; this latter was the only parameter conditioning the response and overall survival. Neither theexpression nor the co-expression of the tested genes was significantly correlated with the response to the induction treatment and long-term outcome.
机译:多药耐药性(MDR)是一种复杂的现象,包括许多调控药物运输或代谢,细胞修复或排毒机制的不同基因的表达。几种基因的共表达可能是体内抗性表型的基础。为了测试几种MDR相关基因(MDR1,拓扑异构酶IIalpha,拓扑异构酶IIbeta,MRP,GSTpi,LRP)的表达和共表达的可能预后作用,对35例急性髓细胞白血病(AML)患者进行了检测RT-PCR分析。在我们的系列中,拓扑异构酶IIbeta与MRP(p = 0.05),GSTpi(p = 0.017)和LRP(p = 0.005)显着共表达。 GSTpi与LRP(p = 0.03)和MRP(p = 0.007)共表达;另一方面,有53.8%的患者LRP和MRP阳性(p = 0.02)。根据患者的生物学/临床特征(包括年龄),PCR阳性率没有差异。后者是调节反应和总生存率的唯一参数。被测基因的表达和共表达均与诱导治疗的反应和长期预后没有显着相关。

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