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首页> 外文期刊>Japanese Journal of Cancer Research >Microarray-based Analysis of Anti-angiogenic Activity of Demethoxycurcumin on Human Umbilical Vein Endothelial Cells: Crucial Involvement of the Down-regulation of Matrix Metalloproteinase.
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Microarray-based Analysis of Anti-angiogenic Activity of Demethoxycurcumin on Human Umbilical Vein Endothelial Cells: Crucial Involvement of the Down-regulation of Matrix Metalloproteinase.

机译:基于微阵列的去甲氧基姜黄素对人脐静脉内皮细胞抗血管生成活性的分析:基质金属蛋白酶下调的关键作用。

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cDNA microarray-based gene expression analysis has been successfully employed to explore the action mechanism and to validate the targets of several drugs. In the present study, we evaluated anti-angiogenic activity of demethoxycurcumin (DC), a structural analog of curcumin, isolated from Curcuma aromatica, and investigated the effect of DC on genetic reprogramming in cultured human umbilical vein endothelial cells (HUVECs) using cDNA microarray analysis. Of 1024 human cancer-focused genes arrayed, 187 genes were up-regulated and 72 genes were down-regulated at least 2-fold by DC. Interestingly, 9 angiogenesis-related genes were down-regulated over 5-fold in response to DC, suggesting that the genetic reprogramming was crucially involved in anti-angiogenesis by the compound. To verify the results obtained from cDNA microarray analysis, matrix metalloproteinase-9 (MMP-9), the product of one of the angiogenesis-related genes down-regulated over 5-fold by DC, was investigated using gelatin zymography. DC
机译:基于cDNA微阵列的基因表达分析已成功用于探索作用机制并验证几种药物的靶标。在本研究中,我们评估了从姜黄中分离的姜黄素的结构类似物去甲氧基姜黄素(DC)的抗血管生成活性,并使用cDNA微阵列芯片研究了DC对培养的人脐静脉内皮细胞(HUVECs)基因重编程的影响。分析。在DC排列的1024个以人类癌症为中心的基因中,有187个基因被上调,而72个基因被下调了至少2倍。有趣的是,响应DC,9种血管生成相关基因被下调了5倍以上,这表明该化合物的抗血管生成至关重要地参与了基因重编程。为了验证从cDNA微阵列分析获得的结果,使用明胶酶谱法研究了基质金属蛋白酶9(MMP-9)(一种被DC下调了5倍的血管生成相关基因之一)的产物。直流电

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