首页> 外文期刊>Journal of applied toxicology >Different mechanisms of action of 2, 2', 4, 4'-tetrabromodiphenyl ether (BDE-47) and its metabolites (5-OH-BDE-47 and 6-OH-BDE-47) on cell proliferation in OVCAR-3 ovarian cancer cells and MCF-7 breast cancer cells
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Different mechanisms of action of 2, 2', 4, 4'-tetrabromodiphenyl ether (BDE-47) and its metabolites (5-OH-BDE-47 and 6-OH-BDE-47) on cell proliferation in OVCAR-3 ovarian cancer cells and MCF-7 breast cancer cells

机译:2、2',4、4'-四溴二苯醚(BDE-47)及其代谢产物(5-OH-BDE-47和6-OH-BDE-47)对OVCAR-3卵巢细胞增殖的不同作用机制癌细胞和MCF-7乳腺癌细胞

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摘要

Data concerning the possible action of polybrominated diphenyl ethers (PBDEs) in hormone-dependent cancer are scarce. Some data showed that PBDEs may directly affect breast cancer cells formation and only one research showed increased proliferation of the OVCAR-3 cells, but the results are ambiguous and the mechanisms are not clear. There is growing evidence that not only parent compounds but also its metabolites may be involved in cancer development. The present study was, therefore, designed to determine the effect of BDE-47 and its metabolites (2.5 to 50ngml(-1)) on proliferation (BrdU), cell-cycle genes (real-time PCR) and protein expression (Western blot), protein expression of oestrogen receptors ( ), extracellular signal-regulated kinases 1 and 2 (ERK1/2) and protein kinase C (PKC) in OVCAR-3 ovarian and MCF-7 breast cancer cells. In OVCAR-3 cells, the parent compound stimulated cell proliferation by activating CDK1, CDK7, E2F1 and E2F2. Independent of time of exposure, BDE-47 had no effect on ER and ER protein expression and ERK1/2 and PKC phosphorylation. Metabolites had no effect on cell proliferation but increased both ERs protein expression and ERK1/2 and PKC phosphorylation. In MCF-7 cells, the parent compound displayed no effect on cell proliferation but decreased ER and increased ER protein expression with concomitant induction of PKC phosphorylation. Both metabolites increased MCF-7 cell proliferation, ERK1/2 and PKC phosphorylation and decreased ER and ER protein expression.We suggest that studies concerning PBDEs with fewer bromine atoms should be continued to understand environmental links to different hormone-dependent cancers. Copyright (c) 2016 John Wiley & Sons, Ltd.
机译:关于多溴二苯醚(PBDEs)在激素依赖性癌症中可能作用的数据很少。一些数据表明,PBDEs可能直接影响乳腺癌细胞的形成,只有一项研究表明OVCAR-3细胞的增殖增加,但结果尚不明确,其机制尚不清楚。越来越多的证据表明,不仅母体化合物而且其代谢物都可能参与癌症的发展。因此,本研究旨在确定BDE-47及其代谢产物(2.5至50ngml(-1))对增殖(BrdU),细胞周期基因(实时PCR)和蛋白质表达(蛋白质印迹)的影响),雌激素受体()的蛋白表达,细胞外信号调节激酶1和2(ERK1 / 2)以及蛋白激酶C(PKC)在OVCAR-3卵巢和MCF-7乳腺癌细胞中的表达。在OVCAR-3细胞中,母体化合物通过激活CDK1,CDK7,E2F1和E2F2刺激细胞增殖。与暴露时间无关,BDE-47对ER和ER蛋白表达以及ERK1 / 2和PKC磷酸化没有影响。代谢物对细胞增殖没有影响,但增加了ERs蛋白表达以及ERK1 / 2和PKC磷酸化。在MCF-7细胞中,母体化合物对细胞增殖无影响,但ER降低和ER蛋白表达增加,并伴随诱导PKC磷酸化。两种代谢物均会增加MCF-7细胞的增殖,ERK1 / 2和PKC的磷酸化并降低ER和ER蛋白的表达。我们建议应继续开展有关溴原子较少的PBDEs的研究,以了解与不同激素依赖性癌症的环境联系。版权所有(c)2016 John Wiley&Sons,Ltd.

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