课题基金 / 基金详情

PREVENTION OF PROSTATIC CARCINOGENESIS BY ANTIOXIDANTS

PREVENTION OF PROSTATIC CARCINOGENESIS BY ANTIOXIDANTS
通过抗氧化剂预防前列腺癌
批准号:
7340378
负责人:
MAARTEN C BOSLAND
金额:
$24.41万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-02-01 至 2010-01-31

项目摘要

项目成果

MAARTEN C BOSLAND的其他基金

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中文摘要
翻译
描述(由申请人提供):该项目提出的假设是,硒、维生素E和番茄红素通过其抗氧化活性预防前列腺癌的发展。关于这一点,人类研究中没有明确的数据。有很少的实验研究,测试这一假设的报告,和那些没有使用模型系统,不涉及氧化应激机制。此外,还没有研究这些抗氧化剂之间可能存在的关键协同作用的报告。因此,本项目的目的是:(a)在涉及氧化应激机制的前列腺癌动物模型中解决这一假设;(B)利用这一模型数据支持抗氧化活性是硒、维生素E和番茄红素预防前列腺癌的主要机制的观点;(d)探索γ-生育酚的功效和抗氧化活性。该项目将使用一种独特的动物模型,适合测试抗氧化剂的化学预防活性,并将有助于严格评估SELECT试验的理由;以及(d)确定这些抗氧化剂单独和组合的保护活性的大小,以提供功效信息,支持预防临床试验的设计。本研究的具体目的是:(1)确定硒、维生素E(α-生育酚)和番茄红素对雌二醇和睾酮处理的NBL大鼠前列腺癌的预防作用。该模型重要地涉及氧化应激机制。抗氧化剂将在饮食中以无毒剂量给予,与先前不涉及氧化应激的前列腺癌模型研究中使用的剂量相当。(2)确定这些抗氧化剂治疗是否降低与DNA碱基氧化、脂质过氧化和抗氧化酶失活或改变相关的氧化应激参数。这些参数将在NBL大鼠的前列腺区域中测量,其中雌二醇和睾酮治疗诱导癌症和肿瘤前病变,并且观察到的效应将与特定目标1的功效研究的结果相关。还将测量前列腺抗氧化剂水平。(3)为了确定γ-生育酚的疗效和抗氧化活性,有流行病学迹象表明,γ-生育酚对前列腺癌的保护作用强于α-生育酚,将γ-生育酚的作用与目的1和2的α-生育酚研究的作用进行比较。(4)确定三种抗氧化剂联合治疗对预防雌二醇和睾酮治疗的NBL大鼠前列腺癌的疗效,并确定这些治疗是否降低氧化应激参数。将观察到的效应与目的1和2的单药研究结果进行比较。
英文摘要
DESCRIPTION (provided by applicant): The hypothesis addressed by this project is that selenium, vitamin E, and lycopene protect against prostate cancer development through their antioxidant activities. There are no definitive data about this from human studies. There are very few reports of experimental studies that tested this hypothesis, and those that did used models systems that do not involve oxidative stress mechanisms. Furthermore, there are no reports of studies that have investigated the probably critical synergisms that may exist between these antioxidants. Therefore, the purpose of this project is: (a) To address this hypothesis in an animal model of prostate carcinogenesis that does involve oxidative stress mechanisms; (b) To generate with this model data in support of the notion that antioxidant activity is a major mechanism by which selenium, vitamin E, and lycopene protect against prostate cancer; (d) To explore the efficacy and antioxidant activity of gamma-tocopherol. The project will use a unique animal model that is suitable to test chemopreventive activity of antioxidants and it will make a contribution to critically assessing the rationale for the SELECT trial; and (d) To determine the magnitude of the protective activity of these antioxidants individually and in combination to provide efficacy information in support of the design of prevention clinical trials. The Specific Aims of the project are: (1) To determine the efficacy of selenium, vitamin E (alpha-tocopherol), and lycopene to prevent prostate cancer in NBL rats treated with estradiol & testosterone. This model importantly involves oxidative stress mechanisms. The antioxidants will be given in the diet at non-toxic doses comparable to those used in previous studies with prostate cancer models that do not involve oxidative stress. (2) To determine whether treatments with these antioxidants reduce oxidative stress parameters related to oxidation of DNA bases, lipid peroxidation, and inactivation or alteration of antioxidant enzymes. These parameters will be measured in the areas of the prostate of NBL rats where treatment with estradiol & testosterone induces cancer and preneoplastic lesions, and the effects observed will be related to the outcome of the efficacy studies of Specific Aim 1. Prostatic antioxidant levels will also be measured. (3) To determine the efficacy and antioxidant activity of gamma-tocopherol There are epidemiological indications that gamma-tocopherol has stronger protective effects against prostate cancer than alpha-tocopherol and the effects of gamma-tocopherol will be compared with those of the alpha-tocopherol studies of Aims 1 and 2. (4) To determine the efficacy of combination treatment with the three antioxidants to prevent prostate cancer in NBL rats treated with estradiol & testosterone and to determine whether these treatments reduce oxidative stress parameters. The observed effects will be compared with the outcome of the single agent studies of Aims 1 and 2.
期刊论文(4)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1080/01635581.2014.904907
发表时间: 2014
期刊: Nutrition and cancer
影响因子: --
作者: [Özten N, Schlicht M, Diamond AM, Bosland MC]
通讯作者: Bosland MC
DOI: 10.1158/1940-6207.capr-16-0088
发表时间: 2016-08
期刊: Cancer prevention research (Philadelphia, Pa.)
影响因子: --
作者: [Bosland MC]
通讯作者: Bosland MC
DOI: 10.4103/1477-3163.90438
发表时间: 2011
期刊: Journal of carcinogenesis
影响因子: --
作者: [Ozten-Kandaş N, Bosland MC]
通讯作者: Bosland MC
DOI: 10.1007/s40495-015-0031-0
发表时间: 2015-08-01
期刊: Current pharmacology reports
影响因子: --
作者: [Bosland MC, Ozten N, Eskra JN, Mahmoud AM]
通讯作者: Mahmoud AM
Effects of SOD2 genotype, oxidative stress, ER??, and genistein on prostate cance
  • 批准号:
    8236933
  • 项目类别:
  • 资助金额:
    $7.85万
  • 财政年份:
    2011
  • 负责人:
    MAARTEN C BOSLAND
  • 依托单位:
Effects of SOD2 genotype, oxidative stress, ER??, and genistein on prostate cance
  • 批准号:
    8115621
  • 项目类别:
  • 资助金额:
    $7.85万
  • 财政年份:
    2011
  • 负责人:
    MAARTEN C BOSLAND
  • 依托单位:
Preventive Activity of Black Raspberries against Prostate Cancer
  • 批准号:
    8101295
  • 项目类别:
  • 资助金额:
    $16.56万
  • 财政年份:
    2010
  • 负责人:
    MAARTEN C BOSLAND
  • 依托单位:
Preventive Activity of Black Raspberries against Prostate Cancer
  • 批准号:
    7963473
  • 项目类别:
  • 资助金额:
    $20.49万
  • 财政年份:
    2010
  • 负责人:
    MAARTEN C BOSLAND
  • 依托单位: