Endocrine Program, Department of Animal Sciences , Rutgers, The State University of New Jersey, New Brunswick, New Jersey.
Alcohol Clin Exp Res. 2013 Nov;37(11):1901-9. doi: 10.1111/acer.12171. Epub 2013 Jul 26.
Prenatal alcohol exposure has been shown to increase offspring susceptibility to some chemical carcinogens. Whether prenatal exposure to alcohol makes the offspring more susceptible to the development of prostate cancer is not known. Therefore, we determined whether any functional abnormalities and increased cancer susceptibility exist in the prostate of fetal alcohol-exposed male rats during the adult period.
Pregnant rats were fed with a liquid diet containing alcohol (alcohol-fed [AF]), or pair-fed with isocaloric liquid diet (PF) or ad libitum fed with rat chow (ad lib-fed). Male offspring of these rats were given N-Nitroso-N-methylurea and testosterone to induce prostate neoplasia or left untreated. Around 6 to 8 months of age, the prostates of these animals were processed for determination of biochemical changes and histopathologies.
Prostates of noncarcinogen treated animals that were alcohol exposed during the prenatal period demonstrated inflammatory cell infiltration and epithelial atypia and increased number of proliferative cells in the ventral lobe of this gland, but the prostate of control animal showed normal cytoarchitecture. In addition, prenatal alcohol-exposed rats showed decreased levels of cell-cell adhesion marker and increased estrogenic activity in the ventral prostate. Prenatally ethanol (EtOH)-exposed rats, when treated with carcinogen and testosterone, showed histological evidence for high-grade prostatic intraepithelial neoplasia (PIN) primarily in the ventral prostate, whereas control animals showed only low-grade PIN. Prenatally EtOH-exposed rats treated with carcinogen and testosterone also showed increased number of proliferative cells and androgen receptor with concomitant decreased levels of tumor suppressor proteins in the ventral prostate.
These results suggest for the first time that prenatal EtOH exposures induce histophysiological changes in the prostate as well as it increases the susceptibility of the prostate to develop neoplasia during adulthood.
已证实产前酒精暴露会增加后代对某些化学致癌物的易感性。然而,产前酒精暴露是否会使后代更容易患上前列腺癌尚不清楚。因此,我们旨在确定在成年期,胎儿酒精暴露是否会导致雄性酒精暴露大鼠的前列腺出现任何功能异常和增加癌症易感性。
给怀孕的大鼠喂食含有酒精的液体饮食(酒精喂养 [AF]),或用等热量的液体饮食(PF)或自由进食大鼠饲料(自由喂养 [ad lib-fed])配对喂养。这些大鼠的雄性后代接受 N-亚硝基-N-甲基脲和睾酮诱导前列腺肿瘤形成,或不进行处理。在大约 6 到 8 个月大时,对这些动物的前列腺进行生化变化和组织病理学检测。
非致癌物处理的动物的前列腺,其在产前阶段受到酒精暴露,表现出炎症细胞浸润和上皮异型性,以及该腺体腹侧叶中增殖细胞数量增加,但对照组动物的前列腺表现出正常的细胞结构。此外,产前酒精暴露的大鼠的细胞间粘附标志物水平降低,而其腹侧前列腺的雌激素活性增加。用致癌剂和睾酮处理的产前酒精暴露大鼠表现出高级别前列腺上皮内瘤变(PIN)的组织学证据,主要发生在腹侧前列腺,而对照组动物仅表现出低级别 PIN。用致癌剂和睾酮处理的产前酒精暴露大鼠的腹侧前列腺还表现出增殖细胞数量增加和雄激素受体增加,同时肿瘤抑制蛋白水平降低。
这些结果首次表明,产前酒精暴露会导致前列腺的组织生理学变化,并增加其在成年期发生肿瘤的易感性。