课题基金 / 基金详情

Role of estrogen receptor beta in cancer prevention by dietary indole-3-carbinol

Role of estrogen receptor beta in cancer prevention by dietary indole-3-carbinol
雌激素受体β在膳食吲哚-3-甲醇预防癌症中的作用
批准号:
7221809
负责人:
Abby D Benninghoff
金额:
$4.68万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-11-15 至 2008-11-14

项目摘要

项目成果

Abby D Benninghoff的其他基金

相似基金

相关文献

中文摘要
翻译
描述(由申请人提供):本研究的长期目标是更好地了解膳食植物化学物质如何影响人类健康和疾病,吲哚-3-甲醇(I3 C)是十字花科蔬菜的关键活性成分,已被证明是一种非常有效的癌症阻断剂,可降低肺癌、结肠癌、乳腺癌和皮肤癌的风险。人们非常担心,胎儿在怀孕期间接触环境化学物质,如烟雾致癌物,可能与儿童和青年癌症有关。最近一项使用经胎盘小鼠癌症模型的研究表明,母体摄入I3 C与致癌物暴露同时发生,显著降低了10个月大后代因侵袭性胸腺淋巴瘤和肺肿瘤多样性导致的后代死亡率。I3 C的化学预防特性可能涉及多种作用机制,包括与芳烃受体(AhR)和雌激素受体(ER)的相互作用。在这项先前的经胎盘癌症研究中,I3 C的化学预防特性不依赖于AhR。因此,虽然I3 C是一种有效的经胎盘化学保护化合物,但其发挥保护作用的机制尚不清楚。为了解决这一关键的知识缺口,将使用ER β基因敲除小鼠模型评价I3 C在预防子宫内暴露于环境致癌物二苯并[a,l]芘(DBP)的后代癌症方面的疗效。ER β是胸腺和肺中表达的主要ER亚型。工作假设是I3 C对DBP诱导的经胎盘致癌作用的保护需要ER β表达。用于检验这一假设的实验方法包括一项为期10个月的经胎盘癌症研究,该研究利用特定的饮食方案来检验I3 C作为化学预防剂在ER β阳性和阴性妊娠环境中肿瘤起始和肿瘤促进阶段的功效。在后代中评估的终点包括淋巴瘤依赖性死亡率、肺和肝肿瘤结局、肿瘤的形态学数据和总体基因表达谱。胎儿是环境化合物的敏感目标,一生中暴露于化学致癌物的很大一部分发生在妊娠期和整个母乳喂养期间。有证据表明,母亲在怀孕期间食用某些蔬菜或植物衍生化合物,如吲哚-3-甲醇,可以预防后代的儿童和成人癌症。然而,目前缺乏对吲哚-3-甲醇对胎儿发挥其癌症阻断作用的机制的了解,这引起了关于其作为人类癌症的预防和/或治疗剂的可能效用的问题。
英文摘要
DESCRIPTION (provided by applicant): The long-term goal of this research is to develop a better understanding of how dietary phytochemicals can influence human health and disease, lndole-3-carbinol (I3C), a key active component of cruciferous vegetables, has been shown to be a remarkably effective cancer blocking agent by reducing risk of lung, colon, breast and skin cancer. There is great concern that fetal exposure to environmental chemicals during pregnancy, such as smoke carcinogens, could be linked to childhood and young adult cancers. A recent study using a transplacental mouse cancer model showed that maternal consumption of I3C coincident with carcinogen exposure markedly decreased offspring mortality due to aggressive thymic lymphoma as well as lung tumor multiplicity in 10 month-old offspring. The chemopreventive properties of I3C can involve multiple mechanisms of action, including interaction with the aryl hydrocarbon receptor (AhR) and the estrogen receptor (ER). In this prior transplacental cancer study, the chemopreventive property of I3C was not dependent on the AhR. Thus, while I3C is an effective chemoprotective compound transplacentally, the mechanism by which it exerts its protective effects is unknown. To address this critical knowledge gap, the therapeutic efficacy of I3C in prevention of cancer in offspring exposed in utero to the environmental carcinogen dibenzo[a,l]pyrene (DBP) will be evaluated using an ERbeta knockout mouse model. ERbeta is the major ER subtype expressed in the thymus and lung. The working hypothesis is that protection by I3C against DBP-induced transplacental carcinogenesis requires ERbeta expression. The experimental approach employed to test this hypothesis consists of a 10 month transplacental cancer study utilizing specific dietary protocols to test the efficacy of I3C as a chemopreventive agent during tumor initiation and tumor promotion phases in both ERbeta positive and negative gestating environments. Endpoints to be evaluated in offspring include lymphoma-dependent mortality, lung and liver tumor outcome, morphometric data and global gene expression profiles of tumors. The fetus is a sensitive target for environmental compounds, and a significant portion of lifetime exposure to chemical carcinogens occurs during gestation and throughout breast feeding. Evidence suggests that maternal consumption of certain vegetables or plant-derived compounds, such as indole-3- carbinol, during pregnancy can prevent childhood and adult cancers in offspring. However, the current lack of understanding of the mechanisms by which indole-3-carbinol exerts its cancer blocking effects to the fetus raises questions about its possible utility as a preventive and/or therapeutic agent for human cancer.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Impact of transplacental PAH exposure on the epigenome
  • 批准号:
    7876561
  • 项目类别:
  • 资助金额:
    $7.0万
  • 财政年份:
    2010
  • 负责人:
    Abby D Benninghoff
  • 依托单位:
Impact of transplacental PAH exposure on the epigenome
  • 批准号:
    8066723
  • 项目类别:
  • 资助金额:
    $6.93万
  • 财政年份:
    2010
  • 负责人:
    Abby D Benninghoff
  • 依托单位:
Cancer prevention by indole-3-carbinol via modulation of the epigenome
  • 批准号:
    7661019
  • 项目类别:
  • 资助金额:
    $16.08万
  • 财政年份:
    2009
  • 负责人:
    Abby D Benninghoff
  • 依托单位:
Cancer prevention by indole-3-carbinol via modulation of the epigenome
  • 批准号:
    7783782
  • 项目类别:
  • 资助金额:
    $18.48万
  • 财政年份:
    2009
  • 负责人:
    Abby D Benninghoff
  • 依托单位:
海外基金