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首页> 外文期刊>Molecular biology reports >Dependence between estrogen sulfotransferase (SULT1E1) and nuclear transcription factor Nrf-2 regulations via oxidative stress in breast cancer
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Dependence between estrogen sulfotransferase (SULT1E1) and nuclear transcription factor Nrf-2 regulations via oxidative stress in breast cancer

机译:通过乳腺癌氧化胁迫抑制雌激素磺基转移酶(SULT1E1)和核转录因子NRF-2规定的依赖性

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摘要

Human estrogen sulfotransferase (SULT1E1) and nuclear factor erythroid 2-related factor 2 (Nrf-2) expression influences each other in advanced human breast carcinogenesis. The difference in the metabolism of estradiol (E2) in pre- and post-menopausal women remains to be connected with post-menopausal breast cancer. A synergism between ROS production and E2 generation has been demonstrated. No definite mechanism for simultaneous functions of Nrf2, oxidative stress E2 regulating enzymes (SULT1E1) has been yet clarified. Our present review demonstrates that ROS dependent regulation of Nrf-2 is one of the most important determinants of E2 regulation by altering SULT1E1 expression. This study also focuses the idea that estrogen receptor cased subtypes of cancer may have different molecular environments which has an impact on the therapeutic efficacy.
机译:人雌激素磺旋转转移酶(SULT1E1)和核因子红细胞2相关因子2(NRF-2)表达在晚期人类乳腺发生中均受彼此影响。 雌二醇(E2)在绝经后妇女中雌二醇(E2)的差异仍然与绝经后乳腺癌相关联。 已经证明了ROS生产与E2代之间的协同作用。 没有确定NRF2的同时函数的确定机制,氧化应激E2调节酶(SULT1E1)已经阐明。 我们现在的审查证明了NRF-2的ROS依赖性调节是通过改变SULT1E1表达来改变E2调节的最重要的决定因素之一。 本研究还专注于雌激素受体甲壳癌癌的思考可能具有不同的分子环境,其对治疗效果产生影响。

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