ROLE OF DNA-BINDING IN SKIN TUMOR INITIATION

DNA 结合在皮肤肿瘤发生中的作用

基本信息

  • 批准号:
    3174653
  • 负责人:
  • 金额:
    $ 14.98万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    1984
  • 资助国家:
    美国
  • 起止时间:
    1984-03-01 至 1993-11-30
  • 项目状态:
    已结题

项目摘要

Humans are continually exposed to a wide variety of chemicals, some of which may act as initiators, promoters, cocarcinogens and/or complete carcinogens. Current evidence suggests that covalent modification of DNA plays a central role in the mechanism of tumor initiation by diverse classes of carcinogenic agents including polycyclic aromatic hydrocarbons (PAH). However, it remains to be determined which DNA-adducts are most important; whether DNA-adducts are removed efficiently or inefficiently thus introducing errors in the DNA; or whether DNA- adducts must persist in the DNA for long periods of time for tumor initiation. The proposed research is designed to further investigate the role of PAH DNA-adduct removal and persistence in relation to skin tumor initiation in mice. Mouse skin is a well known target tissue for PAH and is a widely studied model system for skin carcinogenesis. The specific aims of the proposal are as follows. The quantitative relationship between the formation of specific hydrocarbon DNA-adducts (especially dAdo adducts) and skin tumor-initiation will be determined. The extent and time course of unscheduled DNA synthesis induced by a variety of PAHs will be examined. We will also examine the rates of removal of specific DNA-adducts (especially dAdo adducts) in relation to skin tumor-initiating potency. Furthermore, we will continue to explore the formation, removal, and persistence of hydrocarbon DNA-adducts in epidermal subpopulations in relation to the biphasic disappearance of DNA-adducts in mouse epidermis. We will further examine the role of DNA replication at the time of tumor initiation by determining the quantitative relationship between specific adduct formation and inhibition of epidermal DNA synthesis and through the use of DNA synthesis inhibitors. Finally, to learn more about the biological, biochemical and molecular effects of specific PAH DNA-adducts, we will prepare site directed dAdo adducts from anti BPDE to be incorporated into a bacterial vector. This approach will allow us to test the hypothesis that specific hydrocarbon DNA-adducts are required early after application for skin tumor initiation.
人类不断地接触到各种各样的化学物质,

项目成果

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John DiGiovanni其他文献

John DiGiovanni的其他文献

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{{ truncateString('John DiGiovanni', 18)}}的其他基金

Twist1 as a Target for Prevention and Treatment of Cutaneous Squamous Cell Carcinoma
Twist1作为预防和治疗皮肤鳞状细胞癌的靶点
  • 批准号:
    10651792
  • 财政年份:
    2021
  • 资助金额:
    $ 14.98万
  • 项目类别:
Twist1 as a Target for Prevention and Treatment of Cutaneous Squamous Cell Carcinoma
Twist1作为预防和治疗皮肤鳞状细胞癌的靶点
  • 批准号:
    10424568
  • 财政年份:
    2021
  • 资助金额:
    $ 14.98万
  • 项目类别:
Twist1 as a Target for Prevention and Treatment of Cutaneous Squamous Cell Carcinoma
Twist1作为预防和治疗皮肤鳞状细胞癌的靶点
  • 批准号:
    10288511
  • 财政年份:
    2021
  • 资助金额:
    $ 14.98万
  • 项目类别:
Identification of Natural Compound Combinations for Prevention of Prostate Cancer
预防前列腺癌的天然化合物组合的鉴定
  • 批准号:
    9765960
  • 财政年份:
    2019
  • 资助金额:
    $ 14.98万
  • 项目类别:
Identification of Natural Compound Combinations for Prevention of Prostate Cancer
预防前列腺癌的天然化合物组合的鉴定
  • 批准号:
    10559493
  • 财政年份:
    2019
  • 资助金额:
    $ 14.98万
  • 项目类别:
Identification of Natural Compound Combinations for Prevention of Prostate Cancer
预防前列腺癌的天然化合物组合的鉴定
  • 批准号:
    10320338
  • 财政年份:
    2019
  • 资助金额:
    $ 14.98万
  • 项目类别:
Targeting Fibroblast Growth Factor Receptor-2b in prevention and treatment of cutaneous Squamous cell carcinoma.
靶向成纤维细胞生长因子受体-2b 预防和治疗皮肤鳞状细胞癌。
  • 批准号:
    10318934
  • 财政年份:
    2018
  • 资助金额:
    $ 14.98万
  • 项目类别:
Mechanisms of Obesity-Induced Genetic Instability at Endogenous Mutation Hotspots
肥胖引起的内源突变热点遗传不稳定性的机制
  • 批准号:
    10065499
  • 财政年份:
    2018
  • 资助金额:
    $ 14.98万
  • 项目类别:
Mechanisms of Obesity-Induced Genetic Instability at Endogenous Mutation Hotspots
肥胖引起的内源突变热点遗传不稳定性的机制
  • 批准号:
    10311484
  • 财政年份:
    2018
  • 资助金额:
    $ 14.98万
  • 项目类别:
The Role of CXCL12 Signaling in Obesity-Induced Prostate Cancer Progression
CXCL12 信号在肥胖诱发的前列腺癌进展中的作用
  • 批准号:
    9135275
  • 财政年份:
    2015
  • 资助金额:
    $ 14.98万
  • 项目类别:

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