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首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Dietary zinc deficiency or supplementation during gestation increases breast cancer susceptibility in adult female mice offspring following a J-shaped pattern and through distinct mechanisms
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Dietary zinc deficiency or supplementation during gestation increases breast cancer susceptibility in adult female mice offspring following a J-shaped pattern and through distinct mechanisms

机译:在妊娠期间饮食锌缺乏或补充增加了在J形图案之后的成年女性小鼠后代的乳腺癌敏感性,并通过独特的机制

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摘要

Zinc is required for fetal development and is involved in key processes associated with breast carcinogenesis. We evaluated whether maternal zinc deficiency or supplementation during gestation influences female offspring susceptibility to breast cancer in adulthood. C57BL/6 mice consumed during gestation control (30 p.p.m. zinc), zinc-deficient (8 p.p.m) or zinc-supplemented (45 p.p.m.) diets. Maternal zinc supplementation increased in female mice offspring the incidence of chemically-induced mammary adenocarcinomas that were heavier, compared to control group. This was accompanied by a decreased number of terminal end buds, increased cell proliferation and apoptosis, and increased tumor suppressors p21, p53 and Rassfl, Zfp382 and Stat3 expression in mammary glands, as well as increased zinc status. Although maternal zinc deficiency did not alter the incidence of these lesions, it also induced heavier Mammary adenocarcinomas, compared to control group. These effects were accompanied by a decreased number of terminal end buds, increased proto-oncogenes c-Myc and Lmo4 expression and H3K9Me3 and H4K2OMe3 epigenetic marks in mammary glands of offspring, and decreased zinc status and increased levels of oxidative marker malondialdehyde. The data suggest that both maternal zinc deficiency and supplementation during gestation programmed increased breast cancer susceptibility in adult mice offspring following a J-shaped pattern through distinct mechanisms.
机译:胎儿发育需要锌,并且参与与乳腺癌相关的关键过程。我们评估了妊娠期间孕产妇的锌缺乏或补充是否会影响成年期对乳腺癌的女性后代易感性。在妊娠控制期间消耗的C57BL / 6小鼠(锌),缺锌(8 p.M.M)或锌补充(45 p.M.)饮食。与对照组相比,母体小鼠的母锌补充剂在雌性小鼠中增加了化学诱导的乳腺癌腺癌的发生率。这伴随着末端芽的数量下降,增加细胞增殖和凋亡,肿瘤抑制剂P21,P53和Rassfl,ZFP382和STAT3在乳腺中的表达以及增加的锌状态。虽然母性锌缺乏症未改变这些病变的发生率,但与对照组相比,它也诱导了较重的乳腺癌腺癌。这些效果伴随着末端芽的数量下降,增加了甲状腺炎C-myc和LMO 4表达和H3K9ME3和H3K9ME3和H4K2ME3和H4K2ME3表观遗传标记,并降低了锌状态和氧化标志物丙二醛水平增加。该数据表明,在妊娠期间母体锌缺乏和补充在通过不同机制后,在j形图案之后的成年小鼠后代的乳腺癌易感性增加增加。

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