2-METHOXYESTRADIOL & HORMONAL CANCER
2-METHOXYESTRADIOL & HORMONAL CANCER
批准号:
7392631
负责人:
BAO-TING ZHU
金额:
$20.46万
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-05-01 至 2009-04-30
关键词:
SDS polyacrylamide gel electrophoresisaffinity chromatographyangiogenesisapoptosisbreast neoplasmscatechol methyltransferasecell growth regulationcell linecell proliferationcell surface receptorsenzyme inhibitorsestradiolhigh performance liquid chromatographyhormone related neoplasm /cancerlaboratory ratmass spectrometryneoplastic growthpolymerase chain reactiontissue /cell culture
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): 2-Methoxyestradiol (2-MeO-E2) is a nonpolar endogenous estrogen metabolite formed by metabolic O-methylation of 2-hydroxyestradiol (the most abundant hydroxyestrogen metabolite in humans). 2-MeO-E2 has anti-proliferative, apoptotic, and antiangiogenic actions at nonphysiological high concentrations. This grant application has two overall goals: (i) to study the molecular mechanism(s) of 2-MeO-E2's action by searching for its specific cellular receptor in human breast cancer cell lines. We will isolate a specific, high-affinity cellular receptor for 2-MeO-E2 present in human breast cancer cells, and we will determine its protein and DNA sequences (described under Specific Aim 1). (ii) To determine whether the endogenously-formed or exogenously-administered 2-MeO-E2 (at physiologically-relevant concentrations) has chemoprotective effects against estrogen-induced mammary tumor formation in a commonly-used animal model. We will determine the potency and efficacy of the exogenously-administered 2-MeO-E2 for protection against estradiol-induced mammary tumorigenesis in female ACI rats, and we will also evaluate the mammary cancer-protective effects of the endogenously-formed 2-MeO-E2 by determining whether chronic administration of entacapone (a selective COMT inhibitor) alters estradiol-induced mammary carcinogenesis in the female ACI rats. These studies are described under Specific Aims 2, 3, and 4. Our proposed studies are expected to advance our knowledge on the mammary cancer-protective effects of 2- MeO-E2, a nonpolar endogenous estrogen metabolite formed in large amounts in humans. This knowledge will form the basis for future development of new approaches to the prevention of human mammary cancer by administration of "physiological doses" of 2-MeO-E2 (or its synthetic analogs), or by using agents that can alter the metabolic formation and/or disposition of endogenous 2-MeO-E2 in beneficial ways. The results will also provide novel mechanistic understanding for the biological actions of 2-MeO-E2.
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PDIp is a major intracellular oestrogen-storage protein that modulates tissue levels of oestrogen in the pancreas.
PDIp 是一种主要的细胞内雌激素储存蛋白,可调节胰腺中雌激素的组织水平。
DOI:
10.1042/bj20120868
发表时间:
2012
期刊:
The Biochemical journal
影响因子:
--
作者:
[Fu,Xinmiao, Wang,Pan, Fukui,Masayuki, Long,Cheng, Yin,Linxiang, Choi,HyeJoung, Zhu,BaoTing]
通讯作者:
Zhu,BaoTing
Synergism between the anticancer actions of 2-methoxyestradiol and microtubule-disrupting agents in human breast cancer.
2-甲氧基雌二醇和微管破坏剂在人类乳腺癌中的抗癌作用之间的协同作用。
DOI:
--
发表时间:
2005
期刊:
Cancer research.
影响因子:
--
作者:
[Han,Gui-Zhen, Liu,Zhi-Jian, Shimoi,Kayoko, Zhu,BaoTing]
通讯作者:
Zhu,BaoTing
Both PDI and PDIp can attack the native disulfide bonds in thermally-unfolded RNase and form stable disulfide-linked complexes.
PDI和PDIP都可以攻击热未折叠的RNase中的天然二硫键,并形成稳定的二硫键连接复合物。
DOI:
10.1016/j.bbapap.2011.01.004
发表时间:
2011-04
期刊:
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS
影响因子:
3.2
作者:
[Fu, Xin-Miao, Zhu, Bao Ting]
通讯作者:
Zhu, Bao Ting
DOI:
10.1097/fpc.0b013e32830fbde4
发表时间:
2009-01
期刊:
Pharmacogenetics and genomics
影响因子:
2.6
作者:
[Bai HW, Zhu BT]
通讯作者:
Zhu BT
Characterization of the estradiol-binding site structure of human protein disulfide isomerase (PDI).
DOI:
10.1371/journal.pone.0027185
发表时间:
2011
期刊:
PloS one
影响因子:
3.7
作者:
[Fu XM, Wang P, Zhu BT]
通讯作者:
Zhu BT
共 12 条
Dietary Polyphenols Are Consequential Epigenetic Modulators of Gene Expression
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批准号:7289336
-
项目类别:
-
资助金额:$35.68万
-
财政年份:2006
-
负责人:BAO-TING ZHU
-
依托单位:
Dietary Polyphenols Are Consequential Epigenetic Modulators of Gene Expression
-
批准号:7434725
-
项目类别:
-
资助金额:$36.0万
-
财政年份:2006
-
负责人:BAO-TING ZHU
-
依托单位:
Dietary Polyphenols Are Consequential Epigenetic Modulators of Gene Expression
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批准号:7645082
-
项目类别:
-
资助金额:$34.97万
-
财政年份:2006
-
负责人:BAO-TING ZHU
-
依托单位:
Dietary Polyphenols Are Consequential Epigenetic Modulators of Gene Expression
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批准号:7455988
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项目类别:
-
资助金额:$34.97万
-
财政年份:2006
-
负责人:BAO-TING ZHU
-
依托单位:
2-METHOXYESTRADIOL & HORMONAL CANCER
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批准号:6886982
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项目类别:
-
资助金额:$20.73万
-
财政年份:2003
-
负责人:BAO-TING ZHU
-
依托单位:
2-METHOXYESTRADIOL & HORMONAL CANCER
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批准号:6612121
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项目类别:
-
资助金额:$20.72万
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财政年份:2003
-
负责人:BAO-TING ZHU
-
依托单位:
Selective Induction of Estrogen Conjugative Metabolism
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批准号:6853607
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项目类别:
-
资助金额:$20.73万
-
财政年份:2003
-
负责人:BAO-TING ZHU
-
依托单位:
2-METHOXYESTRADIOL & HORMONAL CANCER
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批准号:6738045
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项目类别:
-
资助金额:$20.73万
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财政年份:2003
-
负责人:BAO-TING ZHU
-
依托单位:
Selective Induction of Estrogen Conjugative Metabolism
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批准号:7024997
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项目类别:
-
资助金额:$0.0万
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财政年份:2003
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负责人:BAO-TING ZHU
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依托单位:
2-METHOXYESTRADIOL & HORMONAL CANCER
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批准号:7054105
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项目类别:
-
资助金额:$0.0万
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财政年份:2003
-
负责人:BAO-TING ZHU
-
依托单位:
Selective Induction of Estrogen Conjugative Metabolism
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批准号:6700241
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项目类别:
-
资助金额:$20.73万
-
财政年份:2003
-
负责人:BAO-TING ZHU
-
依托单位:
Selective Induction of Estrogen Conjugative Metabolism
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批准号:7392612
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项目类别:
-
资助金额:$20.46万
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财政年份:2003
-
负责人:BAO-TING ZHU
-
依托单位:
Selective Induction of Estrogen Conjugative Metabolism
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批准号:6573684
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项目类别:
-
资助金额:$20.71万
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财政年份:2003
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负责人:BAO-TING ZHU
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依托单位:
EFFECTS OF CIGARETTE SMOKING OR PCBS ON HUMAN ESTRADIOL
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批准号:2884571
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项目类别:
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资助金额:$9.59万
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财政年份:1997
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负责人:BAO-TING ZHU
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依托单位:
EFFECTS OF CIGARETTE SMOKING OR PCBS ON HUMAN ESTRADIOL
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批准号:2700757
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项目类别:
-
资助金额:$4.27万
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财政年份:1997
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负责人:BAO-TING ZHU
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依托单位:
CIGARETTE SMOKING OR PCBS EFFECTS ON ESTRADIOL
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批准号:6043268
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项目类别:
-
资助金额:$13.31万
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财政年份:1997
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负责人:BAO-TING ZHU
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依托单位:
SMOKING EFFECTS ON PCBS EFFECTS ON ESTRADIOL METABOLISM
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批准号:2331124
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项目类别:
-
资助金额:$13.54万
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财政年份:1997
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负责人:BAO-TING ZHU
-
依托单位:
海外基金