Neuropeptide Y in neuroblastoma: growth, angiogenesis and future therapeutics.

描述（由申请人提供）：神经母细胞瘤（NB）是儿童肿瘤，尽管有治疗，但通常导致患者死亡。 作为交感神经源，NBs表达神经肽Y（NPY），一种交感神经递质，其作用，然而，在这些肿瘤中仍然未知。 在我们实验室发现NPY对各种细胞的有效生长促进和血管生成活性之后，我们最近发现该肽还刺激NB细胞增殖和肿瘤血管形成，显然是通过相同的Y2和Y 5受体（Rs）。 因此，该提案的总体目标是确定NPY是否是NB中的自分泌/旁分泌生长因子，确定其作用机制和与肿瘤环境的相互作用，验证NPY及其Rs作为潜在的预后标志物，并测试阻断NPY/Y2/Y 5通路是否可能是NB的有效双向治疗。 具体目标将决定：1）人NB组织中NPY及其Rs的表达; 2）NPY与其他NB生长因子的相互作用; 3）Rs相互作用及其细胞内信号传导;以及4）阻断NB中NPY作用的有效方式。 将通过实时RT-PCR和免疫染色研究人NB组织中NPY及其Y2和Y 5 Rs的表达来评估NPY及其Rs对NB的临床相关性以及预后和治疗价值，其与患者存活率、疾病表型和其他已知的预后标志物相关。 为了建立NPY作用及其与其他已知NB生长因子相互作用的机制，我们将确定i）神经营养因子及其Rs是否上调NPY及其Y2/Y 5 Rs，和ii）NPY是否介导神经营养因子的生长促进作用。 将通过蛋白质组学鉴定NB中NPY生长促进和血管生成作用的下游信号传导介质，并使用NB和内皮细胞（EC）增殖、EC迁移和主动脉发芽测定进行测试。 由于初步数据暗示Y2和Y 5 R的异源二聚化是放大NPY诱导的NB和EC增殖的机制-在此，我们将使用用Y2/Y 5 R转染的CHO-K1细胞来证明它们的二聚化，鉴定结合结构域并设计阻断二聚体形成的肽。 将在NB和EC中体外测试阻断肽对NPY诱导的增殖的作用，并且沿着Y2/Y 5 R拮抗剂，在NB异种移植物中体内测试阻断肽对NPY诱导的增殖的作用。 这项研究将首次建立NPY在NB中的作用和机制，并确定该肽及其Rs的预后和治疗价值。

DESCRIPTION (provided by applicant): Neuroblastomas (NBs) are childhood tumors, which, despite therapy, often lead to the death of the patients. Being of sympathetic origin, NBs express neuropeptide Y (NPY), a sympathetic neurotransmitter, whose role, however, in these tumors remains unknown. Following our lab's discovery of NPY's potent growth-promoting and angiogenic activities for various cells, we have recently found that the peptide also stimulates NB cell proliferation and tumor vascularization, apparently via the same Y2 and Y5 receptors (Rs). Thus, the overall goal of this proposal is to establish if NPY is an autocrine/paracrine growth factor in NBs, determine mechanisms of its actions and interactions with tumor environment, validate NPY and its Rs as potential prognostic markers and test if blocking the NPY/Y2/Y5 pathway may be an effective, bi-directional therapy for NB. Specific aims will determine: 1) expression of NPY and its Rs in human NB tissues; 2) interactions of NPY with other NB growth factors; 3) R interactions and their intracellular signaling, and 4) an efficient way of blocking NPY actions in NB. Clinical relevance and the prognostic and therapeutic value of NPY and its Rs for NBs will be assessed by studying expression of NPY and its Y2 and Y5Rs in human NB tissues by Real-time RT-PCR and immunostaining, correlated with patient survival, phenotype of the disease and other known prognostic markers. To establish the mechanisms of NPY actions and its interactions with other known NB growth factors we will determine i) if neurotrophins and their Rs upregulate NPY and its Y2/Y5 Rs, and ii) if NPY mediates nuerotrophins' growth-promoting effects. The downstream signaling mediators of NPY growth-promoting and angiogenic actions in NBs will be identified by proteomics and tested using NB and endothelial cell (EC) proliferation, EC migration and aortic sprouting assays. Since the preliminary data implicated heterodimerization of Y2 and Y5Rs as a mechanism amplifying NPY-induced NB and EC proliferation - here, we will use CHO-K1 cells transfected with the Y2/Y5Rs to prove their dimerization, identify binding domains and design peptides blocking dimer formation. The effect of blocking peptide on NPY-induced proliferation will be tested in vitro in NB and ECs and, along with Y2/Y5R antagonists, in vivo in NB xenografts. The proposed research will be the first to establish the role and mechanisms of NPY's actions in NBs, and determine prognostic and therapeutic values of the peptide and its Rs.