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Re: Targeting PIM kinase enhances the activity of sunitinib in renal cell carcinoma

机译:回复:靶向PIM激酶增强舒尼替尼在肾细胞癌中的活性

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Background: Upregulation of PIM kinase expression has been reported in many malignancies, suggesting that inhibition of PIM kinase activity may be an attractive therapeutic strategy. We hypothesised that inhibition of PIM kinase activity with SGI-1776, a novel small molecule inhibitor of PIM kinase activity, would reduce the viability of renal cell carcinoma (RCC) cells and enhance the activity of sunitinib. Methods: Immunoblotting, qRT-PCR, and gene expression arrays were carried out to identify genes modulated by SGI-1776 treatment. The anticancer activity of SGI-1776 and sunitinib was determined by viability and apoptosis assays and in tumour xenografts in vivo. Results: Treatment with SGI-1776 led to a decrease in phosphorylated and total c-Myc levels, which resulted in the modulation of c-Myc target genes.
机译:背景:在许多恶性肿瘤中均已报道PIM激酶表达上调,这表明抑制PIM激酶活性可能是一种有吸引力的治疗策略。我们假设用SGI-1776(一种新型的PIM激酶活性小分子抑制剂)抑制PIM激酶活性会降低肾细胞癌(RCC)细胞的活力并增强舒尼替尼的活性。方法:进行免疫印迹,qRT-PCR和基因表达阵列,以鉴定由SGI-1776处理的基因。 SGI-1776和舒尼替尼的抗癌活性通过生存力和凋亡测定以及体内肿瘤异种移植来确定。结果:用SGI-1776处理导致磷酸化和总c-Myc水平降低,从而导致c-Myc靶基因的调节。

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  • 来源
    《The Journal of Urology》 |2012年第6期|共2页
  • 作者

    AtalaA.;

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  • 正文语种 eng
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  • 入库时间 2022-08-19 15:17:15

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