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Mol Carcinog. 2017 Jan;56(1):163-171. doi: 10.1002/mc.22480. Epub 2016 Mar 17.

本文引用的文献

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Preliminary physiologically based pharmacokinetic models for benzo[a]pyrene and dibenzo[def,p]chrysene in rodents.初步的生理基于药代动力学模型在啮齿类动物中苯并[a]芘和二苯并[def,p]chrysene。
Toxicol Appl Pharmacol. 2011 Dec 15;257(3):365-76. doi: 10.1016/j.taap.2011.09.020. Epub 2011 Sep 29.
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Differential carcinogenicity of cigarette smoke in mice exposed either transplacentally, early in life or in adulthood.香烟烟雾在胚胎期、生命早期或成年期暴露的小鼠中的差异致癌性。
Int J Cancer. 2012 Mar 1;130(5):1001-10. doi: 10.1002/ijc.26103. Epub 2011 May 30.
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Nutrition, epigenetics, and developmental plasticity: implications for understanding human disease.营养、表观遗传学和发育可塑性:对理解人类疾病的启示。
Annu Rev Nutr. 2010 Aug 21;30:315-39. doi: 10.1146/annurev.nutr.012809.104751.
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Transplacental benzene exposure increases tumor incidence in mouse offspring: possible role of fetal benzene metabolism.胎盘中苯暴露会增加小鼠后代的肿瘤发生率:胎儿苯代谢的可能作用。
Carcinogenesis. 2010 Jun;31(6):1142-8. doi: 10.1093/carcin/bgq074. Epub 2010 Apr 16.
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Comparative contribution of the aryl hydrocarbon receptor gene to perinatal stage development and dioxin-induced toxicity between the urogenital complex and testis in the mouse.芳烃受体基因对小鼠泌尿生殖复合体和睪丸在围产期发育和二恶英诱导毒性中的比较贡献。
Biol Reprod. 2010 Mar;82(3):636-43. doi: 10.1095/biolreprod.109.080812. Epub 2009 Dec 9.
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Fetal mouse Cyp1b1 and transplacental carcinogenesis from maternal exposure to dibenzo(a,l)pyrene.胎儿小鼠Cyp1b1与母体暴露于二苯并(a,l)芘所致的经胎盘致癌作用。
Cancer Prev Res (Phila). 2008 Jul;1(2):128-34. doi: 10.1158/1940-6207.CAPR-07-0004. Epub 2008 Mar 19.
7
Identifying efficacious approaches to chemoprevention with chlorophyllin, purified chlorophylls and freeze-dried spinach in a mouse model of transplacental carcinogenesis.在经胎盘致癌小鼠模型中确定叶绿素铜钠盐、纯化叶绿素和冻干菠菜化学预防的有效方法。
Carcinogenesis. 2009 Feb;30(2):315-20. doi: 10.1093/carcin/bgn280. Epub 2008 Dec 10.
8
Lymphoma and lung cancer in offspring born to pregnant mice dosed with dibenzo[a,l]pyrene: the importance of in utero vs. lactational exposure.给怀孕小鼠喂食二苯并[a,l]芘后其后代患淋巴瘤和肺癌的情况:子宫内暴露与哺乳期暴露的重要性
Toxicol Appl Pharmacol. 2008 Dec 15;233(3):454-8. doi: 10.1016/j.taap.2008.09.009. Epub 2008 Sep 24.
9
Chemoprevention of dibenzo[a,l]pyrene transplacental carcinogenesis in mice born to mothers administered green tea: primary role of caffeine.对饮用绿茶的母鼠所产小鼠经胎盘发生的二苯并[a,l]芘致癌作用进行化学预防:咖啡因的主要作用
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10
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胎盘中二苯并[def,p] Chrysene(DBC)的致癌作用:母体暴露的时间决定了后代中靶组织的反应。

Transplacental carcinogenesis with dibenzo[def,p]chrysene (DBC): timing of maternal exposures determines target tissue response in offspring.

机构信息

Department of Environmental and Molecular Toxicology, Oregon State University, Corvallis, OR 97331, USA.

出版信息

Cancer Lett. 2012 Apr 1;317(1):49-55. doi: 10.1016/j.canlet.2011.11.010. Epub 2011 Nov 13.

DOI:10.1016/j.canlet.2011.11.010
PMID:22085489
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3269513/
Abstract

Dibenzo[def,p]chrysene (DBC) is a transplacental carcinogen in mice (15mg/kg; gestation day (GD) 17). To mimic residual exposure throughout pregnancy, dams received four smaller doses of DBC (3.75mg/kg) on GD 5, 9, 13 and 17. This regimen alleviated the previously established carcinogenic responses in the thymus, lung, and liver. However, there was a marked increase in ovarian tumors (females) and hyperplastic testes (males). [(14)C]-DBC (GD 17) dosing revealed transplacental distribution to fetal tissues at 10-fold lower concentrations than in paired maternal tissue and residual [(14)C] 3weeks post-dose. This study highlights the importance of developmental stage in susceptibility to environmental carcinogens.

摘要

二苯并[def,p]苝(DBC)是一种在小鼠中具有胎盘转移致癌性的物质(15mg/kg;妊娠第 17 天)。为了模拟整个怀孕期间的残留暴露,母鼠在妊娠第 5、9、13 和 17 天接受了四次较小剂量的 DBC(3.75mg/kg)。该方案减轻了先前在胸腺、肺和肝脏中建立的致癌反应。然而,卵巢肿瘤(雌性)和增生睾丸(雄性)明显增加。在妊娠第 17 天给予 [(14)C]-DBC 后,与配对的母体组织相比,胎儿组织中的胎盘转移分布浓度低 10 倍,且 3 周后仍有 [(14)C]残留。这项研究强调了发育阶段对环境致癌物质易感性的重要性。