Hilakivi-Clarke L, Cabanes A, de Assis S, Wang M, Khan G, Shoemaker W J, Stevens R G
Lombardi Cancer Center and Department of Oncology, Georgetown University, 3970 Reservoir Road NW, Washington, DC 20007, USA.
Br J Cancer. 2004 Jun 1;90(11):2225-31. doi: 10.1038/sj.bjc.6601793.
Findings in humans and animal models suggest that in utero hormonal and dietary exposures increase later breast cancer risk. Since alcohol intake by adult women consistently increases their breast cancer risk, we wondered whether maternal alcohol consumption during pregnancy increases female offspring's mammary tumorigenesis. In our study, pregnant female rats were pair-fed isocaloric diets containing either 0 (control), 16 or 25 g alcohol kg(-1) feed between days 7 and 19 of gestation. These alcohol exposures generate blood alcohol levels that correspond to low and moderate alcohol consumption and are lower than those that induce foetal alcohol syndrome. Serum oestradiol levels were elevated in pregnant rats exposed to alcohol (P<0.003). When adult, female offspring of alcohol-exposed dams developed significantly more 7,12-dimethylbenz[a]anthracene -induced mammary tumours, compared to the controls (tumour multiplicity; mean+/-s.e.m., controls: 2.0+/-0.3, 16 g alcohol: 2.7+/-0.4 and 25 g alcohol: 3.7+/-0.4; P<0.006). In addition, the mammary epithelial tree of the alcohol-exposed offspring was denser (P<0.004) and contained more structures that are susceptible for the initiation of breast cancer (P<0.001). Immunohistochemical assessment indicated that the mammary glands of 22-week-old in utero alcohol-exposed rats contained elevated levels of oestrogen receptor-alpha (P<0.04) that is consistent with the changes in mammary gland morphology. In summary, maternal alcohol intake during pregnancy increases female offspring's mammary tumorigenesis, perhaps by programming the foetal mammary gland to exhibit persistent alterations in morphology and gene expression. It remains to be determined whether an increase in pregnancy oestradiol levels mediated alcohol's effects on offspring's mammary tumorigenesis.
人类和动物模型的研究结果表明,子宫内的激素和饮食暴露会增加日后患乳腺癌的风险。由于成年女性饮酒会持续增加其患乳腺癌的风险,我们想知道孕期母亲饮酒是否会增加雌性后代的乳腺肿瘤发生。在我们的研究中,怀孕的雌性大鼠在妊娠第7天至19天期间被配对饲喂含0(对照)、16或25 g酒精·kg⁻¹饲料的等热量饮食。这些酒精暴露产生的血液酒精水平对应于低和中度饮酒量,且低于诱发胎儿酒精综合征的水平。暴露于酒精的怀孕大鼠血清雌二醇水平升高(P<0.003)。成年后,与对照组相比,暴露于酒精的母鼠的雌性后代发生7,12-二甲基苯并[a]蒽诱导的乳腺肿瘤明显更多(肿瘤多发性;平均值±标准误,对照组:2.0±0.3,16 g酒精组:2.7±0.4,25 g酒精组:3.7±0.4;P<0.006)。此外,暴露于酒精的后代的乳腺上皮树更密集(P<0.004),且含有更多易引发乳腺癌的结构(P<0.001)。免疫组织化学评估表明,子宫内暴露于酒精的22周龄大鼠的乳腺中雌激素受体-α水平升高(P<0.04),这与乳腺形态的变化一致。总之,孕期母亲饮酒会增加雌性后代的乳腺肿瘤发生,可能是通过对胎儿乳腺进行编程,使其在形态和基因表达上表现出持续的改变。孕期雌二醇水平的升高是否介导了酒精对后代乳腺肿瘤发生的影响,仍有待确定。