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首页> 外文期刊>Neoplasma: Journal of Experimental and Clinical Oncology >Switching (overtargeting) of estrogen effects and its potential role in hormonal carcinogenesis.
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Switching (overtargeting) of estrogen effects and its potential role in hormonal carcinogenesis.

机译:雌激素作用的转换(过度靶向)及其在激素致癌中的潜在作用。

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Peculiarities of the estrogens influence on target tissues is one of the crucial problems in understanding of the estrogen-induced carcinogenesis and anticarcinogenesis mechanisms. Conditions or factors enhancing the genotoxic component in total effect of estrogens (on the uterine tissue, in particular) are very important, since these factors may influence both the hormonal carcinogenesis type and biological properties of the developing hormone-dependent tumors. In this study female rats (3 months of age at the beginning of experiment) have been given plain water (group 1) or 5% ethanol solution over 4 months. Rats which received ethanol were further divided into 6 groups (groups 2-7). During last 2 months of the experiment N-acetylcysteine was given to rats in group 3, ascorbic acid (vitamin C) and alpha-tocopherol (vitamin E)--to group 4, melatonin--to group 5, carnosine--to group 6; the rats in group 7 swam for 5 days a week according to the so called developing schedule. 2.5 weeks before the end of experiment all rats underwent bilateral ovariectomy, and over 11 days preceding the last day of the experiment they received injections of estradiol (2 microg intramuscularly daily). When the experiment was over, estradiol and cholesterol blood levels, progesterone receptors content, peroxidase activity, proliferation index, percent of cells in S and G2/M phases, thickness of endometrium and rate of DNA damage in uterine tissue (COMET assay) and estradiol 2-hydroxylase activity in liver tissue were measured. The conclusion was that administration of 5% ethanol combined with estrogen injections results in genotoxic (G) changes in the uterus, which may be prevented by giving N-acetylcysteine or melatonin. Combination of vitamins C and E enhances some features of hormonal (H) estrogen effects (uterine weight, induction of progesterone receptors), but attenuates the other (proliferation index). Consequently, the combination of N-acetylcysteine and optimal doses of ascorbic acid and alpha-tocopherol may be recommended for prevention of the phenomenon of switching of estrogen effects [PSEE] (e.g. enhancement of G-component and decrease of H-component), observed particularly in cases of the treatment with tobacco smoke or ethanol consumption in more than moderate (15%) concentrations, which lead to the increased risk of genotoxic type of hormonal carcinogenesis.
机译:雌激素的特异性对靶组织的影响是了解雌激素诱导的致癌作用和抗癌发生机理的关键问题之一。增强雌激素总作用(尤其是对子宫组织)的遗传毒性成分的条件或因素非常重要,因为这些因素可能会影响荷尔蒙癌变类型和正在发展的激素依赖性肿瘤的生物学特性。在这项研究中,在4个月内给雌性大鼠(实验开始时3个月大)服用了白开水(第1组)或5%乙醇溶液。接受乙醇的大鼠进一步分为6组(2-7组)。在实验的最后2个月中,将第3组的大鼠服用N-乙酰半胱氨酸,将抗坏血酸(维生素C)和α-生育酚(维生素E)给药至第4组,褪黑激素-给药至第5组,肌肽-给药6;第7组的老鼠按照所谓的发育时间表每周游泳5天。实验结束前2.5周,所有大鼠均进行了双侧卵巢切除术,并且在实验最后一天之前的11天内,他们接受了雌二醇注射(每天2克肌肉注射)。实验结束后,雌二醇和胆固醇的血液水平,孕激素受体含量,过氧化物酶活性,增殖指数,S和G2 / M期细胞百分比,子宫内膜厚度和子宫组织DNA损伤率(COMET分析)和雌二醇测定肝组织中的2-羟化酶活性。结论是,将5%乙醇与雌激素一起注射会导致子宫的遗传毒性(G)变化,这可以通过服用N-乙酰半胱氨酸或褪黑激素来预防。维生素C和E的组合可增强荷尔蒙(H)雌激素作用的某些功能(子宫重量,孕激素受体的诱导),但会减弱其他功能(增殖指数)。因此,建议将N-乙酰半胱氨酸与最佳剂量的抗坏血酸和α-生育酚结合使用,以预防雌激素效应[PSEE]转换现象(例如,G成分增加而H成分减少)特别是在使用烟熏或乙醇消耗量超过中度(15%)浓度的治疗的情况下,这会导致遗传毒性类型的激素致癌风险增加。

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