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首页> 外文期刊>Biomolecules & therapeutics >Growth Inhibitory Effect of (E)-2,4-bis(p-hydroxyphenyl)-2-Butenaf Diacetate through induction of Apoptotic Cell Death by Increasing DR3 Expression in Human Lung Cancer Cells
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Growth Inhibitory Effect of (E)-2,4-bis(p-hydroxyphenyl)-2-Butenaf Diacetate through induction of Apoptotic Cell Death by Increasing DR3 Expression in Human Lung Cancer Cells

机译:(E)-2,4-双(对羟基苯基)-2-丁烯酸双乙酸盐通过增加人肺癌细胞中DR3的表达诱导凋亡细胞死亡的生长抑制作用

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The Maillard Reaction Products (MRPs) are chemical compounds which have been known to be effective in chemoprevention. Death receptors (DR) play a central role in directing apoptosis in several cancer cells. In our previous study, we demonstrated that (E)-2,4-bis(p-hydroxyphenyl)-2-butenal, a MRP product, inhibited human colon cancer cell growth by inducing apoptosis via nuclear factor-kB (NF-kB) inactivation and G_2/M phase cell cycle arrest. In this study, (E)-2,4-bis(p-hydroxyphenyl)-2-butenal diacetate, a new (E)-2,4-bis(p-hydroxyphenyl)-2-butenal derivative, was synthesized to improve their solubility and stability in water and then evaluated against NCI-H460 and A549 human lung cancer cells. (E)-2,4-bis(p-hydroxyphenyl)-2-butenal diacetate reduced the viability in both cell lines in a time and dose-dependent manner. We also found that (E)-2,4-bis(p-hydroxyphenyl)-2-butenal diacetate increased apoptotic cell death through the upregulation of the expression of death receptor (DR)-3 and DR6 in both lung cancer cell lines. In addition to this, the transfection of DR3 siRNA diminished the growth inhibitory and apoptosis inducing effect of (E)-2,4-bis(p-hydroxyphenyl)-2-butenai diacetate on lung cancer cells, however these effects of (E)-2,4-bis(p-hydroxyphenyl)-2-butenal diacetate was not changed by DR6 siRNA. These results indicated that (E)-2,4-bis(p-hydroxyphenyl)-2-butenal diacetate inhibits human lung cancer cell growth via increasing apoptotic cell death by upregulation of the expression of DR3.
机译:美拉德反应产物(MRP)是已知在化学预防中有效的化合物。死亡受体(DR)在指导几种癌细胞的凋亡中起着核心作用。在我们之前的研究中,我们证明了MRP产物(E)-2,4-双(对羟基苯基)-2-丁烯醛通过诱导核因子-kB(NF-kB)的凋亡来抑制人结肠癌细胞的生长。失活和G_2 / M期细胞周期停滞。在这项研究中,合成了一种新的(E)-2,4-双(对羟基苯基)-2-丁烯醛二乙酸酯(E)-2,4-双(对羟基苯基)-2-丁烯醛衍生物它们在水中的溶解度和稳定性,然后针对NCI-H460和A549人肺癌细胞进行评估。 (E)-2,4-双(对羟基苯基)-2-丁烯二乙酸酯以时间和剂量依赖性方式降低了两种细胞系的活力。我们还发现(E)-2,4-双(对羟基苯基)-2-丁烯二乙酸酯通过上调两种肺癌细胞系中死亡受体(DR)-3和DR6的表达而增加了凋亡细胞的死亡。除此之外,DR3 siRNA的转染减弱了(E)-2,4-双(对羟基苯基)-2-丁烯二乙酸盐对肺癌细胞的生长抑制和凋亡诱导作用,但是(E)的这些作用DR6 siRNA不会改变-2,4-双(对羟基苯基)-2-丁烯二乙酸酯。这些结果表明,(E)-2,4-双(对羟基苯基)-2-丁烯二乙酸盐通过上调DR3的表达来增加凋亡细胞的死亡,从而抑制人肺癌细胞的生长。

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