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首页> 外文期刊>Folia neuropathologica >Antiproliferative effects of [D-Pro2, D-Trp7,9]-Substance P and aprepitant on several cancer cell lines and their selectivity in comparison to normal cells
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Antiproliferative effects of [D-Pro2, D-Trp7,9]-Substance P and aprepitant on several cancer cell lines and their selectivity in comparison to normal cells

机译:[D-Pro2,D-Trp7,9] - upstance p和Awarpitant对几种癌细胞系的抗增殖作用及其与正常细胞相比的选择性

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摘要

A?neuropeptide, Substance P (SP), has mitogenic action in many types of cancer cells mediated via the neurokinin-1 receptor (NK1R). Small molecular NK1R antagonists have been frequently shown to possess anticancer activity both in vivo and in vitro, but there are only a?few papers on such activity regarding peptide antagonists. In order to extend the data on this class of compounds, we have compared the effects of a?peptide antagonist, [D-Pro2, D-Trp7,9]-Substance P, and a?small molecular antagonist, aprepitant on the proliferation of five cancer and three normal cell lines. The comparison was based on three assays: cell proliferation test, MTT test and assay for colony formation. Consistently with earlier reports, aprepitant potently reduced cell proliferation in cancer cell lines in all assays, but in contrast to previous works, the compound was not selective and it affected normal cell lines to a?similar degree. The studied peptide antagonist, [D-Pro2, D-Trp7,9]-Substance P, was able to decrease proliferation only in a?few cell lines, and only in the highest concentration (100 μM). In a?lower concentration, a?slight pro-proliferative effect was observed in a?few cell lines. No statistically significant effects on colony formation were found for this compound.
机译:a?神经肽,物质p(sp),在通过神经蛋白酶-1受体(nk1r)介导的许多类型的癌细胞中具有促致致癌作用。小分子NK1R拮抗剂经常显示体内和体外抗癌活性,但只有一个关于肽拮抗剂的这种活动的纸张。为了扩展这类化合物的数据,我们已经比较了a?肽拮抗剂,[d-pro2,d-trp7,9] - ubstancy p和a的小分子拮抗剂的效果五种癌症和三种正常细胞系。比较基于三个测定:细胞增殖试验,MTT测试和菌落形成的测定。始终如一与早期的报告,当前的试验中,Aprepitant在癌细胞系中具有棘手的细胞增殖,但与先前的作品相比,该化合物没有选择性,并且它将正常细胞系影响到a?相似程度。所研究的肽拮抗剂,[D-Pro2,D-Trp7,9] -substance p能够仅在少量细胞系中降低增殖,并且仅以最高浓度(100μm)。在浓度较低的情况下,在少量细胞系中观察到Δ轻微的促进效果。发现该化合物没有对菌落形成的统计学意义。

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