Repression of ARE-Mediated Gene Expression
Repression of ARE-Mediated Gene Expression
批准号:
7258191
负责人:
MICHAEL L. FREEMAN
金额:
$32.48万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-05-01 至 2012-02-29
关键词:
Adenovirus VectorAnimalsAntioxidantsBindingBiological AssayBleomycinChestClinicalCo-ImmunoprecipitationsDNADNA BindingDataDevelopmentDominant-Negative MutationDrug Metabolic DetoxicationElevationEnzymesExcisionFibrosisGCLC geneGene ExpressionGene TransferGenesGenetic TranscriptionGlutamate-Cysteine LigaseGlutathioneGlutathione DisulfideGlutathione S-TransferaseGoalsImmunoblottingIn VitroInjuryKnockout MiceLeadLungLung diseasesMalignant NeoplasmsMeasurementMeasuresMediatingMethodsModelingMolecularMolecular TargetNorthern BlottingOxidantsOxygenPathway interactionsPatientsPhasePrecipitationProductionProteinsPulmonary FibrosisRadiationRadiation therapyReactive Oxygen SpeciesReporterRepressionResearchResponse ElementsSeveritiesSignal TransductionSmall Interfering RNASuperoxide DismutaseSystemTestingTherapeuticTranscriptional ActivationTransfectionTransforming Growth Factor betaTransforming Growth Factorscatalasecytokinein vivooxidationresearch studyresponsetranscription factoryeast two hybrid system
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The overall goal of the application is to identify the molecular pathways responsible for elevated reactive oxygen specie (ROS) levels that follow in response to TGF-beta signaling in order to aid the development of therapeutic strategies needed to treat this significant clinical problem. ROS contribute to the progression of degenerative pulmonary injury in patients with thoracic malignancies who undergo radiation therapy. Phase II detoxification proteins are responsible for removal of ROS. The transcription factor Nrf2 is a master regulator of Phase II gene expression. Loss of Nrf2 signaling ablates Phase II gene expression, elevates ROS, and enhances progression of pulmonary fibrosis. We show that TGF-beta signaling suppresses Nrf2- regulated Phase II gene expression and elevates ROS. We hypothesize that suppression of Nrf2-regulated transcription is ATF3 mediated, a consequence of TGF-beta signaling through SmadS. Aim 1 will identify the mechanism by which ATF3 suppresses Nrf2-regulated gene expression. The approach will identify the domains required for ATF3 Nrf2 interaction in vitro and in vivo and determine if such an interaction alters Nrf2 function in terms of either Nrf2 DNA binding activity or transcriptional activation. Binding of deletion constructs to GST fusion molecules, co-immunoprecipitation, two hybrid systems, DNA precipitation and ChIP assays will be used. Aim 2 will determine if loss of ATF3 abrogates TGF-beta-mediated suppression of Nrf2-regulated Phase II gene expression and lowers ROS levels. Two approaches will be used to down regulate ATF3: Dominant negative ATF3 molecules and siRNA directed against ATF3. Aim 3 will test the hypothesis that TGF-beta-mediated signaling suppresses Nrf2-regulated gene expression in vivo and that Nrf2 impacts radiation-induced pulmonary fibrosis. The well characterized model of radiation-induced fibrosis will be used to determine if loss of Nrf2 signaling enhances pulmonary injury. Nrf2 wild type and null animals will be used.
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专著(0)
科研奖励(0)
会议论文
The Thromboxane-Prostanoid Receptor in Radiation-Induced Pulmonary Fibrosis
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批准号:10734570
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项目类别:
-
资助金额:$72.59万
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财政年份:2023
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负责人:MICHAEL L. FREEMAN
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依托单位:
Targeting DNA damage response pathways for the treatment of advanced lung cancer
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批准号:8776675
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项目类别:
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资助金额:$22.49万
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财政年份:2014
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负责人:MICHAEL L. FREEMAN
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依托单位:
Nrf2 and Radiation-induced pulmonary fibrosis.
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批准号:8791125
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项目类别:
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资助金额:$43.15万
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财政年份:2013
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负责人:MICHAEL L. FREEMAN
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依托单位:
Nrf2 and Radiation-induced pulmonary fibrosis.
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批准号:8606883
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项目类别:
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资助金额:$42.92万
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财政年份:2013
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负责人:MICHAEL L. FREEMAN
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依托单位:
Nrf2 and Radiation-induced pulmonary fibrosis.
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批准号:8664750
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项目类别:
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资助金额:$3.24万
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财政年份:2013
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负责人:MICHAEL L. FREEMAN
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依托单位:
Nrf2 and Radiation-induced pulmonary fibrosis.
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批准号:8442128
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项目类别:
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资助金额:$39.0万
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财政年份:2013
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负责人:MICHAEL L. FREEMAN
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依托单位:
Development of Small Molecule Radiation Sensitizers
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批准号:8196782
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项目类别:
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资助金额:$36.09万
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财政年份:2009
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负责人:MICHAEL L. FREEMAN
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依托单位:
Development of Small Molecule Radiation Sensitizers
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批准号:8002086
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项目类别:
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资助金额:$34.36万
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财政年份:2009
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负责人:MICHAEL L. FREEMAN
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依托单位:
Development of Small Molecule Radiation Sensitizers
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批准号:7787394
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项目类别:
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资助金额:$35.88万
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财政年份:2009
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负责人:MICHAEL L. FREEMAN
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依托单位:
Development of Small Molecule Radiation Sensitizers
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批准号:8586851
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项目类别:
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资助金额:$33.27万
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财政年份:2009
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负责人:MICHAEL L. FREEMAN
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依托单位:
Development of Small Molecule Radiation Sensitizers
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批准号:8518497
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项目类别:
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资助金额:$1.56万
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财政年份:2009
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负责人:MICHAEL L. FREEMAN
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依托单位:
Development of Small Molecule Radiation Sensitizers
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批准号:8385585
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项目类别:
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资助金额:$32.32万
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财政年份:2009
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负责人:MICHAEL L. FREEMAN
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依托单位:
Repression of ARE-Mediated Gene Expression
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批准号:7577346
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项目类别:
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资助金额:$36.2万
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财政年份:2007
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负责人:MICHAEL L. FREEMAN
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依托单位:
Repression of ARE-Mediated Gene Expression
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批准号:7788176
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项目类别:
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资助金额:$35.06万
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财政年份:2007
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负责人:MICHAEL L. FREEMAN
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依托单位:
Repression of ARE-Mediated Gene Expression
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批准号:7391755
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项目类别:
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资助金额:$35.15万
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财政年份:2007
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负责人:MICHAEL L. FREEMAN
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依托单位:
Repression of ARE-Mediated Gene Expression
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批准号:8033688
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项目类别:
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资助金额:$34.01万
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财政年份:2007
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负责人:MICHAEL L. FREEMAN
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依托单位:
Regulation of Nrf2 Signaling
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批准号:7615551
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项目类别:
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资助金额:$29.79万
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财政年份:2005
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负责人:MICHAEL L. FREEMAN
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依托单位:
Regulation of Nrf2 Signaling
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批准号:7409601
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项目类别:
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资助金额:$28.96万
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财政年份:2005
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负责人:MICHAEL L. FREEMAN
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依托单位:
Regulation of Nrf2 Signaling
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批准号:6965464
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项目类别:
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资助金额:$29.63万
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财政年份:2005
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负责人:MICHAEL L. FREEMAN
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依托单位:
Regulation of Nrf2 Signaling
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批准号:7073985
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项目类别:
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资助金额:$28.65万
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财政年份:2005
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负责人:MICHAEL L. FREEMAN
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依托单位:
海外基金