蒽环类类似物和阿糖胞苷引起的髓系白血病多药耐药表型改变。

Altered multidrug resistance phenotype caused by anthracycline analogues and cytosine arabinoside in myeloid leukemia.

作者信息

Hu X F, Slater A, Kantharidis P, Rischin D, Juneja S, Rossi R, Lee G, Parkin J D, Zalcberg J R

机构信息

Trescowthick Laboratory, Peter MacCallum Cancer Institute, Melbourne, Australia.

出版信息

Blood. 1999 Jun 15;93(12):4086-95.

DOI:
Abstract

The expression of P-glycoprotein (Pgp) is often increased in acute myeloid leukemia (AML). However, little is known of the regulation of Pgp expression by cytotoxics in AML. We examined whether Pgp expression and function in leukemic blasts was altered after a short exposure to cytotoxics. Blasts were isolated from 19 patients with AML (15 patients) or chronic myeloid leukemia in blastic transformation (BT-CML, 4 patients). Pgp expression and function were analyzed by flow cytometric analysis of MRK 16 binding and Rhodamine 123 retention, respectively. At equitoxic concentrations, ex vivo exposure for 16 hours to the anthracyclines epirubicin (EPI), daunomycin (DAU), idarubicin (IDA), or MX2 or the nucleoside analogue cytosine arabinoside (AraC) differentially upregulated MDR1/Pgp expression in Pgp-negative and Pgp-positive blast cells. In Pgp-negative blasts, all four anthracyclines and AraC significantly increased Pgp expression (P =.01) and Pgp function (P =.03). In contrast, MX2, DAU, and AraC were the most potent in inducing Pgp expression and function in Pgp positive blasts (P <.05). A good correlation between increased Pgp expression and function was observed in Pgp-negative (r =.90, P =.0001) and Pgp-positive blasts (r =.77, P =.0002). This increase in Pgp expression and function was inhibited by the addition of 1 micromol/L PSC 833 to blast cells at the time of their exposure to these cytotoxics. In 1 patient with AML, an increase in Pgp levels was observed in vivo at 4 and 16 hours after the administration of standard chemotherapy with DAU/AraC. Upregulation of Pgp expression was also demonstrated ex vivo in blasts harvested from this patient before the commencement of treatment. In 3 other cases (1 patient with AML and 2 with BT-CML) in which blasts were Pgp negative at the time of initial clinical presentation, serial samples at 1 to 5 months after chemotherapy showed the presence of Pgp-positive blasts. All 3 patients had refractory disease. Interestingly, in all 3 cases, upregulation of Pgp by cytotoxics was demonstrated ex vivo in blasts harvested at the time of presentation. These data suggest that upregulation of the MDR1 gene may represent a normal response of leukemic cells to cytotoxic stress and may contribute to clinical drug resistance.

摘要

P-糖蛋白(Pgp)在急性髓系白血病(AML)中的表达通常会增加。然而,关于细胞毒性药物对AML中Pgp表达的调控知之甚少。我们研究了白血病原始细胞短期暴露于细胞毒性药物后Pgp的表达和功能是否发生改变。从19例AML患者(15例)或急变期慢性髓系白血病(BT-CML,4例)中分离出原始细胞。分别通过MRK 16结合的流式细胞术分析和罗丹明123保留情况来分析Pgp的表达和功能。在等效毒性浓度下,将原始细胞离体暴露于表柔比星(EPI)、柔红霉素(DAU)、伊达比星(IDA)或MX2等蒽环类药物或核苷类似物阿糖胞苷(AraC)16小时,可使Pgp阴性和Pgp阳性原始细胞中的多药耐药基因1(MDR1)/Pgp表达出现差异上调。在Pgp阴性原始细胞中,所有四种蒽环类药物和AraC均显著增加Pgp表达(P = 0.01)和Pgp功能(P = 0.03)。相比之下,MX2、DAU和AraC在诱导Pgp阳性原始细胞中的Pgp表达和功能方面最为有效(P < 0.05)。在Pgp阴性(r = 0.90,P = 0.0001)和Pgp阳性原始细胞(r = 0.77,P = 0.0002)中,观察到Pgp表达增加与功能之间具有良好的相关性。在原始细胞暴露于这些细胞毒性药物时加入1 μmol/L的PSC 833可抑制Pgp表达和功能的这种增加。在1例AML患者中,给予DAU/AraC标准化疗后4小时和16小时,体内观察到Pgp水平升高。在该患者治疗开始前采集的原始细胞中,离体实验也证实了Pgp表达上调。在另外3例患者(1例AML患者和2例BT-CML患者)中,初始临床表现时原始细胞为Pgp阴性,化疗后1至5个月的系列样本显示存在Pgp阳性原始细胞。所有3例患者均患有难治性疾病。有趣的是,在所有3例病例中,在就诊时采集的原始细胞中离体实验均证实了细胞毒性药物可上调Pgp。这些数据表明,MDR1基因的上调可能代表白血病细胞对细胞毒性应激的正常反应,并可能导致临床耐药。

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