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白细胞介素-3联合粒细胞-巨噬细胞集落刺激因子治疗可提高阿糖胞苷在体外对急性髓系白血病原始细胞的选择性。

Treatment with interleukin-3 plus granulocyte-macrophage colony-stimulating factors improves the selectivity of Ara-C in vitro against acute myeloid leukemia blasts.

作者信息

Bhalla K, Holladay C, Arlin Z, Grant S, Ibrado A M, Jasiok M

机构信息

Department of Medicine, Medical University of South Carolina, Charleston 29425.

出版信息

Blood. 1991 Nov 15;78(10):2674-9.

PMID:1824260
Abstract

Hematopoietic growth factors (HGFs) interleukin-3 (IL-3) and granulocyte-macrophage colony-stimulating factor (GM-CSF) individually have been shown to increase the percentage of acute myeloid leukemia (AML) blasts in S phase and enhance the cytotoxic effects of Ara-C against these blasts in culture. We compared in vitro the effects of a combined treatment with GM-CSF (10 ng/mL) plus IL-3 (10 ng/mL) on the metabolism and cytotoxicity of Ara-C in normal bone marrow mononuclear cells (NBMMC) and AML blasts. NBMMC from six healthy volunteers and AML blasts from 10 patients were incubated for 20 hours with or without IL-3 plus GM-CSF, followed by a concurrent treatment with Ara-C for 4 additional hours. Exposure to the HGFs and Ara-C produced significantly higher intracellular Ara-CTP levels as well as higher Ara-CTP/dCTP pool ratios in AML blasts as compared with NBMMC. Treatment with HGFs resulted in [3H] Ara-C DNA incorporation that was significantly higher in AML blasts versus NBMMC. This selective improvement of Ara-C metabolism in AML blasts was associated with an enhanced Ara-C-mediated leukemia colony-forming unit (CFU) growth inhibition. In contrast, exposure to HGFs resulted in an improved colony growth of normal CFU granulocyte-monocyte and CFU-granulocyte, erythroid, monocyte, megakaryocyte. These in vitro studies indicate that a combined treatment with IL-3 plus GM-CSF may improve the selectivity of Ara-C against AML blasts.

摘要

造血生长因子(HGFs)白细胞介素-3(IL-3)和粒细胞-巨噬细胞集落刺激因子(GM-CSF)已分别被证明可增加急性髓系白血病(AML)母细胞在S期的百分比,并增强阿糖胞苷(Ara-C)在培养中对这些母细胞的细胞毒性作用。我们在体外比较了GM-CSF(10 ng/mL)加IL-3(10 ng/mL)联合治疗对正常骨髓单个核细胞(NBMMC)和AML母细胞中Ara-C代谢及细胞毒性的影响。来自6名健康志愿者的NBMMC和来自10名患者的AML母细胞在有或无IL-3加GM-CSF的情况下孵育20小时,随后同时用Ara-C再处理4小时。与NBMMC相比,暴露于HGFs和Ara-C后,AML母细胞中细胞内Ara-CTP水平显著更高,Ara-CTP/dCTP池比率也更高。用HGFs处理导致[3H]Ara-C掺入DNA,AML母细胞中的掺入量显著高于NBMMC。AML母细胞中Ara-C代谢的这种选择性改善与Ara-C介导的白血病集落形成单位(CFU)生长抑制增强有关。相反,暴露于HGFs导致正常CFU粒细胞-单核细胞和CFU-粒细胞、红细胞、单核细胞、巨核细胞的集落生长得到改善。这些体外研究表明,IL-3加GM-CSF联合治疗可能会提高Ara-C对AML母细胞的选择性。

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