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首页> 外文期刊>Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis >The role of p38 mitogen-activated protein kinase in serum-induced leukemia inhibitory factor secretion by bone marrow stromal cells from pediatric myelodysplastic syndromes.
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The role of p38 mitogen-activated protein kinase in serum-induced leukemia inhibitory factor secretion by bone marrow stromal cells from pediatric myelodysplastic syndromes.

机译:p38丝裂原活化蛋白激酶在小儿骨髓增生异常综合征骨髓基质细胞分泌血清诱导的白血病抑制因子中的作用。

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摘要

Stromal cells from pediatric myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML) associated with MDS (MDS-AML) present high expression of leukemia inhibitor factor (LIF). We demonstrated using mitogen-activated protein kinase (MAPK) inhibitors that in stromal cells from pediatric MDS and MDS-AML, p38MAPK was critical in serum-induced secretion of LIF. The serum induction of phosphorylated p38MAPK form was observed only in stromal cells from healthy children, whereas in MDS and MDS-AML basal levels were maintained suggesting constitutive p38MAPK activation. Our study suggested the possible importance in pediatric MDS of p38MAPK signaling pathway which may be a future therapeutic target.
机译:来自小儿骨髓增生异常综合症(MDS)和与MDS相关的急性髓性白血病(AML)(MDS-AML)的基质细胞表现出高表达的白血病抑制因子(LIF)。我们证明了使用有丝分裂原激活的蛋白激酶(MAPK)抑制剂,在小儿MDS和MDS-AML的基质细胞中,p38MAPK在血清诱导的LIF分泌中至关重要。仅在健康儿童的基质细胞中观察到了磷酸化的p38MAPK形式的血清诱导,而在MDS和MDS-AML的基础水平保持不变,表明p38MAPK组成性激活。我们的研究表明p38MAPK信号通路在儿科MDS中的重要性,这可能是未来的治疗目标。

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