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首页> 外文期刊>Journal of Hematology and Oncology >Klotho, an anti-aging gene, acts as a tumor suppressor and inhibitor of IGF-1R signaling in diffuse large B cell lymphoma
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Klotho, an anti-aging gene, acts as a tumor suppressor and inhibitor of IGF-1R signaling in diffuse large B cell lymphoma

机译:Klotho是一种抗衰老基因,在弥漫性大B细胞淋巴瘤中作为IGF-1R信号的肿瘤抑制因子和抑制剂

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BackgroundKlotho, is a transmembrane protein, performs as a circulating hormone and upstream modulator of the insulin-like growth factor-1 receptor (IGF-1R), fibroblast growth factor (FGF), and Wnt signaling pathways. These pathways are involved in the development and progression of B cell lymphoma. We aimed to explore the expression pattern and functional mechanism of Klotho in diffuse large B cell lymphoma (DLBCL). MethodsImmunohistochemistry (IHC) and western blotting were performed to detect the expression level of Klotho in DLBCL patients and cell lines. Tumor suppressive effect of Klotho was determined by both in vitro and in vivo studies. Signaling pathway activity was assessed by western blotting. ResultsRemarkable lower expression levels of Klotho were observed in DLBCL patients and cell lines. Enforced expression of Klotho could significantly induce cell apoptosis and inhibit tumor growth in DLBCL. Upregulation of Klotho resulted in declined activation of IGF-1R signaling, accompanied with decreased phosphorylation of its downstream targets, including AKT and ERK1/2. Moreover, xenograft model treated with either Klotho overexpression vector or recombinant human Klotho administration presented restrained tumor growth and lower Ki67 staining. ConclusionsOur findings establish that Klotho performs as a tumor suppressor and modulator of IGF-1R signaling in DLBCL. Targeting Klotho may provide novel strategies for future therapeutic intervention.
机译:背景Klotho是一种跨膜蛋白,可作为胰岛素样生长因子1受体(IGF-1R),成纤维细胞生长因子(FGF)和Wnt信号通路的循环激素和上游调节剂。这些途径与B细胞淋巴瘤的发生和发展有关。我们旨在探讨Klotho在弥漫性大B细胞淋巴瘤(DLBCL)中的表达模式和功能机制。方法采用免疫组化和免疫印迹法检测DLBCL患者和细胞株中Klotho的表达水平。通过体外和体内研究确定了Klotho的肿瘤抑制作用。通过蛋白质印迹评估信号通路活性。结果在DLBCL患者和细胞系中观察到明显较低的Klotho表达水平。 Klotho的表达增强可显着诱导DLBCL细胞凋亡并抑制肿瘤的生长。 Klotho的上调导致IGF-1R信号传导的激活降低,并伴随其下游靶标(包括AKT和ERK1 / 2)的磷酸化降低。而且,用Klotho过表达载体或重组人Klotho给药处理的异种移植模型表现出抑制的肿瘤生长和较低的Ki67染色。结论我们的发现确定Klotho在DLBCL中可作为IGF-1R信号传导的肿瘤抑制因子和调节剂。靶向克洛索可能为未来的治疗干预提供新的策略。

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