Modulation of PEDF activities as potential therapeutic targets in prostate cancer.
Modulation of PEDF activities as potential therapeutic targets in prostate cancer.
批准号:
8848509
负责人:
Stephanie Filleur
金额:
$4.98万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-06-20 至 2016-11-30
关键词:
AffectAnimalsApoptosisBiological AssayBlood CirculationCancer Cell GrowthCancer PatientCell LineCell SurvivalCellsChemotaxisCollaborationsCombined Modality TherapyDataDevelopmentDiseaseDisorder by SiteDistantDoseDsRedDunning Prostate CancerEndothelial CellsEngineeringGoalsGrowthHistopathologyHormonesHumanImmuneIn VitroInflammationInflammatoryInjection of therapeutic agentInstitutionInterleukin-8InvestigationKidneyLNCaPLaboratoriesLeadLiverLungMalignant NeoplasmsMalignant neoplasm of prostateMeasuresMediator of activation proteinMetastatic Neoplasm to the BoneMetastatic Prostate CancerModelingMolecular TargetMonitorMusNeoplasm MetastasisNormal tissue morphologyOrganPC3 cell linePatientsPharmaceutical PreparationsPhenotypePlacebosPopulationPre-Clinical ModelPredictive FactorProductionPropertyProstateProstate Cancer therapyProstatic NeoplasmsProteinsPublishingRattusResearchResistanceRodent ModelRoleSiteSpecimenSpleenSystemTaxane CompoundTestingTherapeuticTravelTreatment EfficacyTumor Cell InvasionTumor ImmunityTumor VolumeUmbilical veinUp-RegulationVariantVascularizationWestern BlottingWorkXenograft procedureandrogen independent prostate cancerangiogenesisarginasebasebonecancer cellcancer therapycell growthcell motilitycell typechemotherapycytotoxicdensitydocetaxelfluorescence imagingimprovedin vivoinhibitor/antagonistlymph nodesmacrophagematrigelmigrationmodel developmentmonocyteneoplastic cellnew therapeutic targetnovelpigment epithelium-derived factorprostate cancer cellprostate cancer modelpublic health relevancered fluorescent proteintaxanetherapeutic targettumortumor growthtumor initiationtumor microenvironmenttumor progression
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Neo-vascularization (angiogenesis) and inflammation in the tumor microenvironment have been described as favorable for tumor cell growth and survival. As a direct result, tumor cells are able to travel through the circulation to colonize distant organs and sites (metastases). A natural protein known as Pigment Epithelium-Derived Factor (PEDF) is expressed in normal tissues and decreased in prostate tumors. We have shown that PEDF is a potent angio- inhibitory factor. Other studies suggest a role for PEDF in inflammation; however its precise mode of action is still unclear and need further investigation. In a previous work, we demonstrated that engineering prostate cancer cells to increase PEDF blocks tumor growth and prolong survival in vivo. We also have shown that PEDF stimulates the recruitment of monocytes and macrophages inflammatory cells in vitro. Thus PEDF expression, prostate cancer progression and tumor inflammation seem interrelated. However, their precise relationship during prostate cancer growth and metastasis formation is still unclear. In the proposed study, we will first evaluate in mouse prostate cancer models, the capacity of PEDF to block the formation of bone metastases, a common and therapeutically challenging site of disease in patients with advanced prostate cancer. We will also identify the mechanisms by which PEDF expression affects the anti-tumor immunity activity in human prostate cancer. We will evaluate the in vitro and in vivo anti-tumor activities of PEDF in combination with low dose taxane drugs. The taxane drugs are currently used as standard chemotherapies for patients with metastatic prostate cancer. These studies which combine both in vitro, in vivo and mouse preclinical models, should allow us to provide data in support of PEDF as novel target for prostate cancer treatment. We also anticipate that this project will lead to the development of improved therapeutic approaches for prostate cancer.
PUBLIC HEALTH RELEVANCE: The major goals of this project are to validate PEDF as a novel therapeutic target for prostate cancer and to investigate PEDF anti-cancer efficacy in combination with low dose chemotherapeutic taxane drugs in preclinical models of prostate cancer. We will also identify the mechanisms by which PEDF affects the anti-tumor immunity activity in human prostate cancer.
期刊论文(4)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1371/journal.pone.0174968
发表时间:
2017
期刊:
PloS one
影响因子:
3.7
作者:
[Martinez-Marin D, Jarvis C, Nelius T, de Riese W, Volpert OV, Filleur S]
通讯作者:
Filleur S
DOI:
10.1002/pros.22595
发表时间:
2013-04
期刊:
PROSTATE
影响因子:
2.8
作者:
[Nelius, Thomas, Samathanam, Christina, Martinez-Marin, Dalia, Gaines, Natalie, Stevens, Jessica, Hickson, Johnny, de Riese, Werner, Filleur, Stephanie]
通讯作者:
Filleur, Stephanie
DOI:
10.1038/cddis.2014.180
发表时间:
2014-05-08
期刊:
Cell death & disease
影响因子:
9
作者:
[]
通讯作者:
Modulation of Pigment Epithelium-Derived Factor's activities as potential therape
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批准号:8287300
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项目类别:
-
资助金额:$44.55万
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财政年份:2012
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负责人:Stephanie Filleur
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依托单位:
Modulation of Pigment Epithelium-Derived Factor's activities as potential therape
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批准号:8729648
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项目类别:
-
资助金额:$5.02万
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财政年份:2012
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负责人:Stephanie Filleur
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依托单位:
海外基金