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Differently labeled peptide ligands for rapid investigation of receptor expression on a new human glioblastoma cell line.

机译:不同标记的肽配体可用于快速研究新型人胶质母细胞瘤细胞系上受体的表达。

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摘要

The neuropeptides vasoactive intestinal peptide (VIP), neuropeptide Y (NPY), and substance P (SP) as well as insulin and insulin-like growth factor 1 (IGF-1) were labeled with biotin, fluorescent dyes, and radioactivity to characterize the expression of peptide receptor of a novel cancer cell line, established from a human glioblastoma multiforme. Thus, not only binding sites could be detected but advantages and disadvantages of the different labels could be compared, too. With all three markers, the presence or absence of the receptors could be answered rapidly and sensitively. The glioblastoma cells express receptors for VIP (IC(50) = 9 nM +/- 30%), insulin (K(d) = 0.66 nM +/- 14%, B(max) = 0.028 nM +/- 13%), and IGF-1 (K(d) = 21 nM +/- 25%, B(max) = 1.65 nM +/- 24%), but there are no binding sites for NPY and SP. As especially VIP and IGF-1 receptors are expressed in huge amounts, these receptors might be an interesting target for tumor diagnostics and therapy.
机译:用生物素,荧光染料和放射性标记神经肽血管活性肠肽(VIP),神经肽Y(NPY)和物质P(SP)以及胰岛素和胰岛素样生长因子1(IGF-1)。人多形性胶质母细胞瘤建立的新型癌细胞系肽受体的表达因此,不仅可以检测结合位点,而且还可以比较不同标记的优缺点。使用所有三个标记,可以快速而灵敏地回答受体的存在与否。胶质母细胞瘤细胞表达VIP(IC(50)= 9 nM +/- 30%),胰岛素(K(d)= 0.66 nM +/- 14%,B(max)= 0.028 nM +/- 13%)的受体,和IGF-1(K(d)= 21 nM +/- 25%,B(max)= 1.65 nM +/- 24%),但没有NPY和SP的结合位点。由于特别是VIP和IGF-1受体大量表达,这些受体可能成为肿瘤诊断和治疗的有趣靶标。

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