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首页> 外文期刊>The Journal of Nutritional Biochemistry >High levels of arachidonic acid and peroxisome proliferator-activated receptor-alpha in breast cancer tissues are associated with promoting cancer cell proliferation.
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High levels of arachidonic acid and peroxisome proliferator-activated receptor-alpha in breast cancer tissues are associated with promoting cancer cell proliferation.

机译:乳腺癌组织中高含量的花生四烯酸和过氧化物酶体增殖物激活的受体-α与促进癌细胞增殖有关。

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Fatty acids are endogenous ligands of peroxisome proliferator-activated receptor-alpha (PPAR alpha), which is linked to the regulation of fatty acid uptake, lipid metabolism and breast cancer cell growth. This study was designed to screen candidate fatty acids from breast cancer tissue and to investigate the effects of these candidate fatty acids on PPAR alpha expression, cell growth and cell cycle progression in breast cancer cell lines. One breast cancer tissue and one reference tissue were each taken from 30 individual breasts to examine for fatty acid composition and PPAR alpha expression. The cancer cell lines MDA-MB-231 (ER-), MCF-7 (ER++++) and BT-474 (ER++) were used to explore the mechanisms regulating cell proliferation. We found that arachidonic acid (AA) and PPAR alpha were highly expressed in the breast cancer tissues. AA stimulated the growth of all three breast cancer cells in a time- and dose-dependent manner. The growth stimulatory effect of AA was associated with PPAR alpha activation, and the most potent effect was found in MCF-7 cells. The stimulation of cell proliferation by AA was accompanied by the increased expression of cyclin E, a reduced population of G1 phase cells, and a faster G1/S phase transition. In contrast, AA had no effects on the levels of CDK2, CDK4, cyclin D1, p27, Bcl-2 and Bax. Our results demonstrate that high levels of AA and PPAR alpha expression in human breast cancer tissues are associated with ER-overexpressed breast cancer cell proliferation, which is involved in activating PPAR alpha, stimulating cyclin E expression, and promoting faster G1/S transition. All rights reserved, Elsevier.
机译:脂肪酸是过氧化物酶体增殖物激活受体-α(PPARα)的内源性配体,与脂肪酸摄取,脂质代谢和乳腺癌细胞生长的调节有关。这项研究旨在从乳腺癌组织中筛选候选脂肪酸,并研究这些候选脂肪酸对乳腺癌细胞系中PPARα表达,细胞生长和细胞周期进程的影响。从30个单独的乳房中分别取出一个乳腺癌组织和一个参考组织,以检查脂肪酸组成和PPARα表达。使用癌细胞系MDA-MB-231(ER-),MCF-7(ER ++++)和BT-474(ER ++)探索调节细胞增殖的机制。我们发现花生四烯酸(AA)和PPARα在乳腺癌组织中高表达。 AA以时间和剂量依赖性方式刺激了所有三种乳腺癌细胞的生长。 AA的生长刺激作用与PPARα激活相关,在MCF-7细胞中发现最有效的作用。 AA对细胞增殖的刺激伴随着细胞周期蛋白E表达的增加,G1期细胞数量的减少和G1 / S相变的更快。相反,AA对CDK2,CDK4,细胞周期蛋白D1,p27,Bcl-2和Bax的水平没有影响。我们的结果表明,人乳腺癌组织中高水平的AA和PPARα表达与ER过表达的乳腺癌细胞增殖有关,这与激活PPARα,刺激细胞周期蛋白E表达并促进更快的G1 / S过渡有关。保留所有权利,Elsevier。

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