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首页> 外文期刊>Turkish Journal of Hematology >Regulation of Tumor Necrosis Factor-related Apoptosis-inducing Ligand Expression in Primary Acute Leukemic Cells by Chemotherapeutics
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Regulation of Tumor Necrosis Factor-related Apoptosis-inducing Ligand Expression in Primary Acute Leukemic Cells by Chemotherapeutics

机译:化学疗法对肿瘤坏死因子相关的凋亡诱导配体在原发性急性白血病细胞中表达的调节。

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Objective: The expression of the tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) protein and its regulation by chemotherapeutics were analyzed in primary acute leukemic cells.Materials and Methods: Peripheral blood was collected from 16 patients with acute leukemia on days 0, 1, 3, and 5 of chemotherapy. The mononuclear cells were separated from the peripheral blood, and TRAIL expression was assessed by flow cytometry. The bone marrow mononuclear cells of patients with acute leukemia were separated before chemotherapy and cultured in vitro with VP-16 and/or interferon (IFN). The TRAIL expression level was detected after the cell culture.Results: TRAIL expression in the mononuclear cells of peripheral blood was significantly upregulated on day 1 (p0.05).Conclusion: OA single chemotherapy mechanism for leukemia may suffice to induce TRAIL expression and promote the apoptosis of leukemic cells.
机译:目的:分析原发性急性白血病细胞中肿瘤坏死因子相关的凋亡诱导配体(TRAIL)蛋白的表达及其化学治疗的调控作用。材料与方法:于第0天从16例急性白血病患者中采集外周血, 1、3和5的化疗。从外周血中分离单核细胞,并通过流式细胞术评估TRAIL表达。化疗前分离出急性白血病患者的骨髓单个核细胞,并在体外用VP-16和/或干扰素(IFN)培养。细胞培养后检测TRAIL表达水平。结果:外周血单核细胞中TRAIL表达在第1天显着上调(p0.05)。结论:OA单一白血病化疗机制可能足以诱导TRAIL表达和促进白血病细胞的凋亡。

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