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首页> 外文期刊>International Journal of Hematology >Extracellular NM23-H1 protein inhibits the survival of primary cultured normal human peripheral blood mononuclear cells and activates the cytokine production
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Extracellular NM23-H1 protein inhibits the survival of primary cultured normal human peripheral blood mononuclear cells and activates the cytokine production

机译:细胞外NM23-H1蛋白抑制原代培养的正常人外周血单个核细胞的存活并激活细胞因子的产生

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摘要

An elevated serum level of NM23-H1 protein is found in acute myelogenous leukemia (AML) and predicts a poor treatment outcome for AML patients. To investigate the potential pathological link between the elevated serum level of this protein and poor prognosis, we examined the extracellular effects of recombinant NM23-H1 protein on the in vitro survival of primary cultured normal peripheral blood mononuclear cells (PBMNC) at concentrations equivalent to the levels found in the serum of AML patients. Extracellular NM23-H1 protein inhibited the in vitro survival of PBMNC and promoted the production of various cytokines, such as GM-CSF and IL-1β, which in fact promoted the growth of primary cultured AML cells. These findings indicate a novel biological action of extracellular NM23-H1 and its association with poor prognosis of patients with elevated serum levels of NM23-H1 protein. These results suggest an important role of extracellular NM23-H1 in the malignant progression of leukemia and a potential therapeutic target for these malignancies.
机译:在急性粒细胞性白血病(AML)中发现了NM23-H1蛋白的血清水平升高,并预测AML患者的治疗结局较差。为了研究这种蛋白的血清水平升高与预后不良之间的潜在病理联系,我们研究了重组NM23-H1蛋白对原代培养的正常外周血单个核细胞(PBMNC)的体外存活率的等效于其的体外作用。 AML患者血清中的血脂水平。细胞外NM23-H1蛋白抑制了PBMNC的体外存活,并促进了各种细胞因子(如GM-CSF和IL-1β)的产生,实际上促进了原代培养的AML细胞的生长。这些发现表明细胞外NM23-H1的新型生物学作用及其与血清NM21-H1蛋白水平升高的患者预后不良相关。这些结果表明细胞外NM23-H1在白血病的恶性进展中的重要作用和这些恶性肿瘤的潜在治疗目标。

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