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首页> 外文期刊>Oncogene >IL-6-independent expression of Mcl-1 in human multiple myeloma
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IL-6-independent expression of Mcl-1 in human multiple myeloma

机译:多发性骨髓瘤中Mcl-1的IL-6依赖性表达

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摘要

Mcl-1 is a critical antiapoptotic survival factor for human multiple myeloma (MM). We examined the importance of IL-6 for Mcl-1 expression in five MM cell lines and in primary MM cells from 14 patients. While culture of MM.1S cells in IL-6 did induce Mcl-1 expression, four other MM cell lines exhibited high levels of Mcl-1 expression that were unaffected by IL-6. Similarly, Mcl-1 expression in 10 of 14 primary MM isolates was found to be IL-6-independent. An analysis of the mechanisms responsible for IL-6-independent Mcl-1 expression was undertaken. ERK1/2 activity did not influence Mcl-1 expression, distinct from Mcl-1 regulation that occurs during myeloid differentiation from hematopoietic progenitor cells. Inhibition of the PI3K pathway led to growth inhibition of 8226 and ANBL-6 cells without reduction of Mcl-1 levels, and high level Mcl-1 expression was maintained in the absence of activated STAT3. Analysis of the transcriptional activity of 5'-regulatory sequences from the human Mcl-1 gene in MM cells demonstrated high levels of IL-6-independent indicator gene activation as predicted. These data demonstrate that the mechanisms regulating Mcl-1 levels in MM cells are heterogeneous, and are often independent from IL-6 signaling pathways.
机译:Mcl-1是人类多发性骨髓瘤(MM)的关键抗凋亡生存因子。我们检查了IL-6在5种MM细胞系和14例原发性MM细胞中Mcl-1表达的重要性。虽然在IL-6中培养MM.1S细胞确实诱导了Mcl-1表达,但其他四个MM细胞系却表现出高水平的Mcl-1表达,不受IL-6的影响。同样,发现14个原发性MM分离物中有10个Mcl-1表达独立于IL-6。进行了负责独立于IL-6的Mcl-1表达的机制的分析。 ERK1 / 2活性并不影响Mcl-1的表达,这与Mcl-1的调节不同,Mcl-1的调节是在骨髓从造血祖细胞分化过程中发生的。 PI3K途径的抑制导致8226和ANBL-6细胞的生长抑制而不降低Mcl-1水平,并且在没有激活的STAT3的情况下维持了高水平的Mcl-1表达。 MM细胞中来自人类Mcl-1基因的5'调控序列的转录活性分析表明,IL-6独立的指示基因激活水平很高。这些数据表明调节MM细胞中Mcl-1水平的机制是异质的,并且通常独立于IL-6信号通路。

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