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P2X7受体是PI3K/GSK3β/VEGF信号网络的关键调节因子:实验性神经母细胞瘤的证据

The P2X7 receptor is a key modulator of the PI3K/GSK3β/VEGF signaling network: evidence in experimental neuroblastoma.

作者信息

Amoroso F, Capece M, Rotondo A, Cangelosi D, Ferracin M, Franceschini A, Raffaghello L, Pistoia V, Varesio L, Adinolfi E

机构信息

Department of Morphology, Surgery and Experimental Medicine, Section of Experimental Pathology, Oncology and Biology, University of Ferrara, Ferrara, Italy.

Laboratory of Molecular Biology, Giannina Gaslini Institute, Genoa, Italy.

出版信息

Oncogene. 2015 Oct 8;34(41):5240-51. doi: 10.1038/onc.2014.444. Epub 2015 Jan 26.

Abstract

Neuroblastoma (NB) is an aggressive pediatric tumor, responsible for 15% of cancer-related deaths in childhood, lacking an effective treatment in its advanced stages. The P2X7 receptor for extracellular ATP was associated to NB cell proliferation and recently emerged as a promoter of tumor engraftment, growth and vascularization. In an effort to identify new therapeutic options for neuroblastoma, we studied the role of P2X7 receptor in NB biology. We first analyzed the effect of P2X7 activation or down-modulation of the main biochemical ways involved in NB progression: the PI3K/Akt/GSK3β/MYCN and the HIF1α/VEGF pathways. In ACN human NB cells, P2X7 stimulation enhanced PI3K/Akt, while decreasing GSK3β activity. In the same model, P2X7 silencing or antagonist administration reduced the activity of PI3K/Akt and increased that of GSK3β, leading to a decrease in cellular glycogen stores. Similarly, P2X7 downmodulation caused a reduction in HIF1α levels and vascular endothelial growth factor (VEGF) secretion. Systemic administration of two different P2X7 antagonists (AZ10606120 or A740003) in nude/nude mice reduced ACN-derived tumor growth. An even stronger effect of P2X7 blockade was obtained in a syngeneic immune-competent neuroblastoma model: Neuro2A cells injected in AlbinoJ mice. Together with tumor regression, treatment with P2X7 antagonists caused downmodulation of the Akt/HIF1α axis, leading to reduced VEGF content and decreased vessel formation. Interestingly, in both experimental models, P2X7 antagonists strongly reduced the expression of the probably best-accepted oncogene in NB: MYCN. Finally, we associated P2X7 overexpression with poor prognosis in advanced-stage NB patients. Taken together, our data suggest that P2X7 receptor is an upstream regulator of the main signaling pathways involved in NB growth, metabolic activity and angiogenesis, and a promising therapeutic target for neuroblastoma treatment.

摘要

神经母细胞瘤(NB)是一种侵袭性儿童肿瘤,占儿童癌症相关死亡的15%,晚期缺乏有效的治疗方法。细胞外ATP的P2X7受体与NB细胞增殖有关,最近被发现是肿瘤植入、生长和血管生成的促进因子。为了寻找神经母细胞瘤的新治疗方案,我们研究了P2X7受体在NB生物学中的作用。我们首先分析了P2X7激活或下调对NB进展所涉及的主要生化途径的影响:PI3K/Akt/GSK3β/MYCN和HIF1α/VEGF途径。在ACN人NB细胞中,P2X7刺激增强了PI3K/Akt,同时降低了GSK3β活性。在同一模型中,P2X7沉默或给予拮抗剂降低了PI3K/Akt的活性,增加了GSK3β的活性,导致细胞糖原储备减少。同样,P2X7下调导致HIF1α水平和血管内皮生长因子(VEGF)分泌减少。在裸鼠/裸鼠中全身给予两种不同的P2X7拮抗剂(AZ10606120或A740003)可减少ACN来源的肿瘤生长。在同基因免疫活性神经母细胞瘤模型(将Neuro2A细胞注射到AlbinoJ小鼠中)中,P2X7阻断的效果更强。与肿瘤消退一起,用P2X7拮抗剂治疗导致Akt/HIF1α轴下调,导致VEGF含量降低和血管形成减少。有趣的是,在两个实验模型中,P2X7拮抗剂都强烈降低了NB中可能最被认可的癌基因:MYCN的表达。最后,我们发现P2X7过表达与晚期NB患者的不良预后相关。综上所述,我们的数据表明,P2X7受体是NB生长、代谢活性和血管生成所涉及的主要信号通路的上游调节因子,是神经母细胞瘤治疗的一个有前景的治疗靶点。

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