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SENP1 inhibition induces apoptosis and growth arrest of multiple myeloma cells through modulation of NF-kappa B signaling

机译:SENP1抑制通过调节NF-κB信号传导诱导多发性骨髓瘤细胞凋亡和生长停滞

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摘要

SUMO/sentrin specific protease 1 (Senp1) is an important regulation protease in the protein sumoylation, which affects the cell cycle, proliferation and differentiation. The role of Senp1 mediated protein desumoylation in pathophysiological progression of multiple myeloma is unknown. In this study, we demonstrated that Senp1 is overexpressed and induced by IL-6 in multiple myeloma cells. Lentivirus-mediated Senp1 knockdown triggers apoptosis and reduces viability, proliferation and colony forming ability of MM cells. The NF-kappa B family members including P65 and inhibitor protein IkB alpha play important roles in regulation of MM cell survival and proliferation. We further demonstrated that Senp1 inhibition decreased IL-6-induced P65 and IkB alpha phosphorylation, leading to inactivation of NF-kappa B signaling in MM cells. These results delineate a key role for Senp1 in IL-6 induced proliferation and survival of MM cells, suggesting it may be a potential new therapeutic target in MM. (C) 2015 Elsevier Inc. All rights reserved.
机译:SUMO / Sentrin特异性蛋白酶1(Senp1)是蛋白sumoylation中重要的调控蛋白酶,它影响细胞周期,增殖和分化。 Senp1介导的蛋白质去合成在多发性骨髓瘤的病理生理进程中的作用尚不清楚。在这项研究中,我们证明了Senp1在多种骨髓瘤细胞中过表达并被IL-6诱导。慢病毒介导的Senp1敲低触发细胞凋亡,并降低MM细胞的活力,增殖和集落形成能力。包括P65和抑制剂蛋白IkB alpha在内的NF-κB家族成员在MM细胞存活和增殖的调节中起着重要作用。我们进一步证明,Senp1抑制降低了IL-6诱导的P65和IkBα磷酸化,从而导致MM细胞中NF-κB信号失活。这些结果描述了Senp1在IL-6诱导的MM细胞增殖和存活中的关键作用,表明它可能是MM中潜在的新治疗靶标。 (C)2015 Elsevier Inc.保留所有权利。

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