Role of leukotriene B4 receptors in the interplay of inflammation and infection
白三烯 B4 受体在炎症和感染相互作用中的作用
基本信息
- 批准号:8433515
- 负责人:
- 金额:$ 27.87万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2009
- 资助国家:美国
- 起止时间:2009-04-01 至 2016-01-31
- 项目状态:已结题
- 来源:
- 关键词:APC geneAcuteAdoptive TransferAffinityAnaphylaxisAntibioticsArthritisAsthmaAtherosclerosisAzoxymethaneBiological ModelsBone MarrowCancer EtiologyCancer ModelCellsCessation of lifeChimera organismChronicColon CarcinomaColonic NeoplasmsColorectal CancerConsumptionDefectDevelopmentDietDiseaseEnvironmentEnvironmental Risk FactorEventExposure toFunctional disorderGenesGenetic VariationHealthHomeostasisHost DefenseHumanImmuneImmune System DiseasesImmune responseImmune systemImmunologic SurveillanceInfectionInfiltrationInflammationInflammation MediatorsInflammatoryInflammatory disease of the intestineIntegration Host FactorsIntestinal CancerIntestinal NeoplasmsIntestinesLTB4R geneLaboratoriesLeukotriene B4Leukotriene B4 ReceptorsLeukotrienesLinkMalignant - descriptorMalignant NeoplasmsMediatingMediator of activation proteinModelingMolecular CarcinogenesisMusMutationPathogenesisPathway interactionsPhenotypePlayProcessProteinsRoleShapesSodium Dextran SulfateTestingToll-Like Receptor PathwayTransgenic MiceTumor PromotersUnited Statesairway hyperresponsivenessbasebody systemcell typeenvironmental agentgut microbiotagut microfloraimmune functionmRNA Expressionmicrobialmicrobial colonizationmicrobicidemicroorganism interactionmouse modelnovelnovel strategiesprotein expressionreceptortumor
项目摘要
DESCRIPTION (provided by applicant): Colon cancer is a leading cause of cancer related deaths in the United States. Exposure to a number of hazardous environmental agents and consumption of the Western diet are known to contribute to the pathogenesis of malignant colon cancer. While chronic inflammation is known to be a major promoter of tumor development the role of gut microflora in contributing to the colon cancer is unknown. Our laboratory has identified leukotriene B4 receptor, BLT1 as a major regulator of inflammation and host response to infections. In a mouse model of spontaneous intestinal cancer (ApcMin/+), we have made the observation that absence of BLT1 greatly enhances intestinal tumor development. This has led to the central hypothesis that Absence of BLT1 enhances colon tumor development by defective immune surveillance and/or altered microbial gut homeostasis. This apparently paradoxical result that loss of a proinflammatory mediator increases inflammation and tumor development suggests that the ever changing micro environment of intestine can have a major influence on the development of colorectal cancer. The current proposal will test this hypothesis in three specific aims. In aim 1, we will examine the mechanisms of leukotriene B4 pathway mediated protection of intestinal cancers in ApcMin/+ mice. Aim 2 will establish the immune functions in tumor bearing mice in the context of BLT1+/+ and BLT1-/- mice. Aim 3 will test the novel concept that defective host response and altered gut microbiota are responsible for rapid development of colon tumors in BLT1-/- mice. These studies will provide a comprehensive model system to examine the interplay of inflammation and infections to the development of colon cancer. Since the mouse ApcMin/+ model is highly related to human colon cancers the result will have direct and immediate impact for the treatment of human colon cancer.
描述(由申请人提供):结肠癌是美国癌症相关死亡的主要原因。众所周知,接触许多有害的环境因素和食用西方饮食会导致恶性结肠癌的发病机制。虽然已知慢性炎症是肿瘤发展的主要促进因素,但肠道微生物群在导致结肠癌中的作用尚不清楚。我们的实验室已确定白三烯 B4 受体 BLT1 是炎症和宿主感染反应的主要调节因子。在自发性肠癌(ApcMin/+)的小鼠模型中,我们观察到BLT1的缺失极大地促进了肠道肿瘤的发展。这导致了一个中心假设:BLT1 的缺失会通过缺陷的免疫监视和/或改变微生物肠道稳态来促进结肠肿瘤的发展。这一看似矛盾的结果表明,促炎介质的丧失会增加炎症和肿瘤的发展,这表明肠道不断变化的微环境可能对结直肠癌的发展产生重大影响。当前的提案将在三个具体目标上检验这一假设。在目标 1 中,我们将研究白三烯 B4 通路介导的 ApcMin/+ 小鼠肠癌保护机制。目标 2 将在 BLT1+/+ 和 BLT1-/- 小鼠的背景下建立荷瘤小鼠的免疫功能。目标 3 将测试新概念,即宿主反应缺陷和肠道微生物群改变是 BLT1-/- 小鼠结肠肿瘤快速发展的原因。这些研究将提供一个全面的模型系统来检查炎症和感染与结肠癌发展的相互作用。由于小鼠ApcMin/+模型与人类结肠癌高度相关,其结果将对人类结肠癌的治疗产生直接而立竿见影的影响。
项目成果
期刊论文数量(5)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Crystalline silica-induced leukotriene B4-dependent inflammation promotes lung tumour growth.
- DOI:10.1038/ncomms8064
- 发表时间:2015-04-29
- 期刊:
- 影响因子:16.6
- 作者:Satpathy SR;Jala VR;Bodduluri SR;Krishnan E;Hegde B;Hoyle GW;Fraig M;Luster AD;Haribabu B
- 通讯作者:Haribabu B
Expression of leukotriene B₄ receptor-1 on CD8⁺ T cells is required for their migration into tumors to elicit effective antitumor immunity.
- DOI:10.4049/jimmunol.1300967
- 发表时间:2013-09-15
- 期刊:
- 影响因子:0
- 作者:Sharma RK;Chheda Z;Jala VR;Haribabu B
- 通讯作者:Haribabu B
Chemoattractant Receptors BLT1 and CXCR3 Regulate Antitumor Immunity by Facilitating CD8+ T Cell Migration into Tumors.
- DOI:10.4049/jimmunol.1502376
- 发表时间:2016-09-01
- 期刊:
- 影响因子:0
- 作者:Chheda ZS;Sharma RK;Jala VR;Luster AD;Haribabu B
- 通讯作者:Haribabu B
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HARIBABU BODDULURI其他文献
HARIBABU BODDULURI的其他文献
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{{ truncateString('HARIBABU BODDULURI', 18)}}的其他基金
Role of leukotriene B4 receptors in the interplay of inflammation and infection
白三烯 B4 受体在炎症和感染相互作用中的作用
- 批准号:
8210894 - 财政年份:2009
- 资助金额:
$ 27.87万 - 项目类别:
Role of leukotriene B4 receptors in the interplay of inflammation and infection
白三烯 B4 受体在炎症和感染相互作用中的作用
- 批准号:
8015283 - 财政年份:2009
- 资助金额:
$ 27.87万 - 项目类别:
Role of leukotriene B4 receptors in the interplay of inflammation and infection
白三烯 B4 受体在炎症和感染相互作用中的作用
- 批准号:
7635082 - 财政年份:2009
- 资助金额:
$ 27.87万 - 项目类别:
Leukotriene B4 Receptors in Rheumatoid Arthritis
类风湿关节炎中的白三烯 B4 受体
- 批准号:
7032234 - 财政年份:2003
- 资助金额:
$ 27.87万 - 项目类别:
Leukotriene B4 Receptors in Rheumatoid Arthritis
类风湿关节炎中的白三烯 B4 受体
- 批准号:
6610703 - 财政年份:2003
- 资助金额:
$ 27.87万 - 项目类别:
Leukotriene B4 Receptors in Rheumatoid Arthritis
类风湿关节炎中的白三烯 B4 受体
- 批准号:
6706978 - 财政年份:2003
- 资助金额:
$ 27.87万 - 项目类别:
Leukotriene B4 Receptors in Rheumatoid Arthritis
类风湿关节炎中的白三烯 B4 受体
- 批准号:
6858582 - 财政年份:2003
- 资助金额:
$ 27.87万 - 项目类别:
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