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首页> 外文期刊>Life sciences >A natural propenoic acid derivative activates peroxisome proliferator-activated receptor-beta/delta (PPARbeta/delta).
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A natural propenoic acid derivative activates peroxisome proliferator-activated receptor-beta/delta (PPARbeta/delta).

机译:天然的丙酸衍生物可激活过氧化物酶体增殖物激活的受体β/δ(PPARbeta /δ)。

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AIMS: Previous studies showed that natural prenyloxyphenylpropanoid derivatives have potent biological properties in vivo. Given the structural similarities between these compounds and known peroxisome proliferator-activated receptor (PPAR) agonists, the present study examined the hypothesis that propenoic acid derivatives activate PPARs. MAIN METHODS: Chimeric reporter assays were performed to identify propenoic acid derivates that could activate PPARs. Quantitative polymerase chain reaction (qPCR) analysis of wild-type and Pparbeta/delta-null mouse primary keratinocytes was performed to determine if a test compound could specifically activate PPARbeta/delta. A human epithelial carcinoma cell line and primary mouse keratinocytes were used to determine the effect of the compound on cell proliferation. KEY FINDINGS: Three of the propenoic acid derivatives activated PPARs, with the greatest efficacy being observed with prenyloxycinnamic acid derivatives 4'-geranyloxyferulic acid (compound 1) for PPARbeta/delta. Compound 1 increased expression of a known PPARbeta/delta target gene through a mechanism that requires PPARbeta/delta. Inhibition of cell proliferation by compound 1 was found in a human epithelial carcinoma cell line. SIGNIFICANCE: Results from these studies demonstrate that compound 1 can activate PPARbeta/delta and inhibit cell proliferation of a human skin cancer cell line, suggesting that the biological effects of 4'-geranyloxyferulic acid may be mediated in part by activating this PPAR isoform.
机译:目的:先前的研究表明,天然异戊烯氧基苯基丙烷衍生物在体内具有强大的生物学特性。考虑到这些化合物与已知的过氧化物酶体增殖物激活受体(PPAR)激动剂之间的结构相似性,本研究检查了烯酸衍生物激活PPAR的假说。主要方法:进行嵌合报告基因分析,以鉴定可以激活PPAR的丙烯酸衍生物。进行了野生型和Pparbeta / delta无效的小鼠原代角质形成细胞的定量聚合酶链反应(qPCR)分析,以确定受试化合物是否可以特异性激活PPARbeta / delta。使用人上皮癌细胞系和原代小鼠角质形成细胞来确定该化合物对细胞增殖的作用。主要发现:三种丙烯酸衍生物激活了PPAR,其中异戊烯基肉桂酸衍生物4'-香叶基氧基阿魏酸(化合物1)对PPARbeta /δ的作用最大。化合物1通过需要PPARbeta / delta的机制增加了已知PPARbeta / delta靶基因的表达。在人上皮癌细胞系中发现了化合物1对细胞增殖的抑制。意义:这些研究的结果表明,化合物1可以激活PPARbeta / delta并抑制人皮肤癌细胞系的细胞增殖,表明4'-香叶基氧基阿魏酸的生物作用可能部分地通过激活该PPAR亚型而介导。

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