Role of Neurogenic Inflammation in Pancreatic Cancer
神经源性炎症在胰腺癌中的作用
基本信息
- 批准号:9093716
- 负责人:
- 金额:$ 41.55万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2013
- 资助国家:美国
- 起止时间:2013-08-15 至 2018-06-30
- 项目状态:已结题
- 来源:
- 关键词:AblationAffectAfferent NeuronsAppearanceAttenuatedAutomobile DrivingBloodBlood CirculationBrain-Derived Neurotrophic FactorCalcitonin Gene-Related PeptideCellsClinicalConditioned Culture MediaDataDevelopmentDiagnosisDiseaseDisease ProgressionDistantEdemaElectrophysiology (science)Epithelial CellsExposure toFiberGene ExpressionGenesGeneticGenetically Engineered MouseGlutamatesGrowthHealthHumanHypersensitivityImmune systemIndividualInflammationInflammatoryLabelLaboratoriesLeadLesionLinkLiverMaintenanceMalignant NeoplasmsMalignant neoplasm of pancreasMethodologyMethodsModelingMusNatureNerve Growth Factor ReceptorsNerve Growth FactorsNervous system structureNeurogenic InflammationNeuronsNodose GanglionOrganPancreasPancreatectomyPancreatic Ductal AdenocarcinomaPancreatic Intraepithelial NeoplasiaPatientsPhysiciansPlayPremalignantProcessProductionPropertyRiskRoleSensorySignal TransductionStagingSubstance PTRP channelTestingTimeTissuesUnited StatesUp-RegulationWestern Blottingacute pancreatitisafferent nervebasechronic pancreatitiscytokineglial cell-line derived neurotrophic factorhigh riskmouse modelneurotrophic factorneutralizing antibodynovelpancreatic neoplasmpatch clamppreventprophylacticrelating to nervous systemresearch studyresponsesensory inputspinal nerve posterior roottumortumor growthtumor progression
项目摘要
DESCRIPTION (provided by applicant): Pancreatic ductal adenocarcinoma (PDAC), like many cancers, has a major inflammatory component that is integral to disease progression. In humans, patients with familial chronic pancreatitis (CP) have a 53-fold increase in their risk for PDAC [92] and 40% go on to develop pancreatic cancer [63]. The link between CP and PDAC is so strong that physicians often recommend prophylactic pancreatectomy for patients with severe CP. The mechanistic link between pancreatic inflammation and cancer is not known. However, studies by our laboratories and others indicate that inflammation accelerates the disease, driving maturation of precancerous lesions into frank cancer [40, 41]. Furthermore, in a genetically engineered mouse model (GEM) of PDAC, pancreatic inflammation increased dissemination of pancreatic cells into the blood and liver [78].
Experiments in our labs show that pancreatic inflammation can be regulated by the nervous system. The importance of "neurogenic inflammation" is supported by studies that show ablation or silencing of pancreatic afferents attenuates/prevents acute and chronic pancreatitis [45, 67, 81, 82]. PDAC converts the pancreas into a tissue that produces pathological levels of neurotrophic factors that cause hypersensitivity and sprouting of sensory neuron terminals and this likely underlie disease-related neurogenic inflammation. Importantly, preliminary data from our lab indicate that growth factor upregulation begins early in the disease process, even before the appearance of frank cancer (Preliminary Data). These observations in combination with the role that inflammation appears to play in progression of PDAC leads to the central hypothesis of this application: PDAC-generated neurotrophic factors induce neurogenic inflammation that drives PDAC progression. This hypothesis will be tested in the following specific aims:
Aim 1: Determine the effect of PDAC-produced neurotrophic factors on pancreatic afferents (dorsal root and nodose ganglion neurons) and whether blocking these growth factors attenuates the release of neurogenic inflammatory molecules.
Aim 2: Determine the contribution of neurogenic inflammation to PDAC progression and tumor growth.
These studies will directly test the role of the nervous system in PDAC. Three different methodologies will be tested for their ability to block neurogenic inflammation and slow/halt disease progression. Each of these methods is either currently available or in development for use in the clinical setting. If successful, any of these approaches could be used for patients with
high-risk for PDAC or those in which the disease is already diagnosed.
描述(由申请人提供):与许多癌症一样,胰腺导管腺癌(PDAC)具有与疾病进展不可或缺的主要炎症成分。在人类中,患有家族性慢性胰腺炎(CP)的患者患PDAC的风险增加了53倍[92],40%的患者继续发展为胰腺癌[63]。CP和PDAC之间的联系是如此紧密,以至于医生经常建议对重度CP患者进行预防性胰腺切除术。胰腺炎症和癌症之间的机制联系尚不清楚。然而,我们的实验室和其他人的研究表明,炎症加速了疾病,促使癌前病变成熟为坦率的癌症[40,41]。此外,在PDAC的基因工程小鼠模型(GEM)中,胰腺炎症增加了胰腺细胞向血液和肝脏中的传播[78]。
我们实验室的实验表明,胰腺炎症可以由神经系统调节。“神经源性炎症”的重要性得到了研究的支持,这些研究表明胰腺传入神经的消融或沉默可减轻/预防急性和慢性胰腺炎[45,67,81,82]。PDAC将胰腺转化为产生病理水平的神经营养因子的组织,所述神经营养因子引起超敏反应和感觉神经元末端的发芽,并且这可能是疾病相关的神经源性炎症的基础。重要的是,我们实验室的初步数据表明,生长因子上调在疾病过程的早期就开始了,甚至在坦率的癌症出现之前。这些观察结果与炎症似乎在PDAC进展中发挥的作用相结合,导致本申请的中心假设:PDAC产生的神经营养因子诱导神经源性炎症,从而驱动PDAC进展。将在以下具体目标中检验这一假设:
目标1:确定PDAC产生的神经营养因子对胰腺传入神经(背根和结状神经节神经元)的影响,以及阻断这些生长因子是否会减弱神经源性炎症分子的释放。
目的2:确定神经源性炎症对PDAC进展和肿瘤生长的贡献。
这些研究将直接测试神经系统在PDAC中的作用。将测试三种不同方法阻断神经源性炎症和减缓/停止疾病进展的能力。这些方法中的每一种都是目前可用的或正在开发用于临床环境。如果成功的话,这些方法中的任何一种都可以用于
PDAC的高风险或那些已经诊断出疾病的人。
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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BRIAN M DAVIS其他文献
BRIAN M DAVIS的其他文献
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- 资助金额:
$ 41.55万 - 项目类别:
Role of Neurogenic Inflammation in Pancreatic Cancer
神经源性炎症在胰腺癌中的作用
- 批准号:
8721899 - 财政年份:2013
- 资助金额:
$ 41.55万 - 项目类别:
Role of Neurogenic Inflammation in Pancreatic Cancer
神经源性炎症在胰腺癌中的作用
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8559041 - 财政年份:2013
- 资助金额:
$ 41.55万 - 项目类别:
Role of Neurogenic Inflammation in Pancreatic Cancer
神经源性炎症在胰腺癌中的作用
- 批准号:
9302686 - 财政年份:2013
- 资助金额:
$ 41.55万 - 项目类别:
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Phenotyping pain in a mouse model of pancreatic cancer
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