首页> 外文期刊>The Journal of Steroid Biochemistry and Molecular Biology >Quercetin-3-O-glucronide inhibits noradrenaline binding to alpha_2-adrenergic receptor, thus suppressing DNA damage induced by treatment with 4-hydroxyestradiol and noradrenaline in MCF-10A cells
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Quercetin-3-O-glucronide inhibits noradrenaline binding to alpha_2-adrenergic receptor, thus suppressing DNA damage induced by treatment with 4-hydroxyestradiol and noradrenaline in MCF-10A cells

机译:槲皮素-3-O-葡糖醛酸抑制去甲肾上腺素与α_2-肾上腺素受体的结合,从而抑制MCF-10A细胞中4-羟基雌二醇和去甲肾上腺素对DNA的损伤

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摘要

Risk factors for breast cancer include estrogens such as 17beta-estradiol (E_2) and high stress levels. 4-Hydroxyestradiol (4-OHE_2), a metabolite of E_2 formed preferentially by cytochrome P4501 B1, is oxidized to E_2-3,4-quinone, which reacts with DNA to form depurinating adducts that exert genotoxicity and car-cinogenicity. Endogenous catecholamines such as adrenaline (A) and noradrenaline (NA) are released from the adrenal gland and sympathetic nervous system during exposure to stress.
机译:乳腺癌的危险因素包括雌激素,例如17β-雌二醇(E_2)和高压力水平。 4-羟基雌二醇(4-OHE_2)是由细胞色素P4501 B1优先形成的E_2代谢产物,被氧化成E_2-3,4-醌,与DNA反应形成脱嘌呤加合物,产生遗传毒性和致癌性。内源性儿茶酚胺如肾上腺素(A)和去甲肾上腺素(NA)在接触压力时会从肾上腺和交感神经系统中释放出来。

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