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
- 来源:
- 关键词:DNA repair DNA replication autoradiography benzanthracenes benzopyrenediol epoxide carbopolycyclic compound chemical addition chemical carcinogenesis cocarcinogen high performance liquid chromatography laboratory mouse molecular pathology neoplastic transformation radioassay skin neoplasms tissue /cell culture tritium tumor promoters
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
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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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
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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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