首页> 外文期刊>Leukemia >PI3-K|[sol]|AKT|[sol]|FKHR and MAPK signaling cascades are redundantly stimulated by a variety of cytokines and contribute independently to proliferation and survival of multiple myeloma cells
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PI3-K|[sol]|AKT|[sol]|FKHR and MAPK signaling cascades are redundantly stimulated by a variety of cytokines and contribute independently to proliferation and survival of multiple myeloma cells

机译:PI3-K | [sol] | AKT | [sol] | FKHR和MAPK信号级联受到多种细胞因子的过度刺激,并独立参与多发性骨髓瘤细胞的增殖和存活

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IL-6 has been reported to play a central role in growth and survival of multiple myeloma (MM) cells. However, recently we have demonstrated that in the presence of bone marrow stromal cells, survival of MM cells becomes independent of the IL-6/gp130/STAT3 pathway questioning the singular role of IL-6 in MM. Therefore, it was the aim of this study to identify additional factors and signaling pathways that might contribute to the growth and survival of MM cells. We found that in addition to IL-6 a number of bone marrow derived cytokines such as LIF, VEGF, bFGF, MIP-1, SDF-1, IL-1, SCF and IL-3 activate the MAPK pathway and induce proliferation of MM.1S and RPMI-8226 MM cells. In addition, these cytokines independently phosphorylate the forkhead family member FKHR via PI3-K/AKT and support survival of primary human MM cells. Inhibition of these pathways induces apoptosis in MM cell lines and primary MM cells. Thus, we provide evidence that in addition to IL-6 a number of different factors trigger important growth-promoting pathways to support the proliferation and survival of MM cells. Therefore, blocking such pathways, rather than blocking a single factor, might be a promising approach for the development of novel treatment strategies in MM.
机译:据报道,IL-6在多发性骨髓瘤(MM)细胞的生长和存活中起着核心作用。然而,最近我们已经证明,在骨髓基质细胞的存在下,MM细胞的存活变得独立于IL-6 / gp130 / STAT3途径,质疑IL-6在MM中的独特作用。因此,本研究的目的是确定可能有助于MM细胞生长和存活的其他因素和信号传导途径。我们发现除IL-6外,许多骨髓衍生的细胞因子(如LIF,VEGF,bFGF,MIP-1,SDF-1,IL-1,SCF和IL-3)激活MAPK途径并诱导MM增殖.1S和RPMI-8226 MM单元。此外,这些细胞因子通过PI3-K / AKT独立地使叉头家族成员FKHR磷酸化,并支持原代人MM细胞的存活。这些途径的抑制诱导MM细胞系和原代MM细胞的凋亡。因此,我们提供的证据表明,除了IL-6外,许多其他因素还触发了重要的促生长途径,以支持MM细胞的增殖和存活。因此,阻断这样的途径,而不是阻断单个因素,可能是发展MM新治疗策略的一种有前途的方法。

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