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Targeting the BMP pathway in metastatic cancer

Targeting the BMP pathway in metastatic cancer
靶向转移性癌症中的 BMP 通路
批准号:
10433812
负责人:
Philip Owens
金额:
$0.0万
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-07-01 至 2022-06-30
关键词:
AcuteAdaptive Immune SystemAreaBladderBone DiseasesBone Morphogenetic ProteinsBreast Cancer ModelCalcitoninCardiovascular systemCell Differentiation processCell LineageCell ProliferationCell physiologyCharacteristicsChronicColonComplexDataDevelopmentDiseaseDisseminated Malignant NeoplasmDistantDrug Delivery SystemsFlow CytometryGeneral PopulationGenetically Engineered MouseGoalsGrowthHealth systemHistopathologyHumanImmuneImmunologic SurveillanceImmunosuppressionImpairmentImplantIn VitroInjectionsLesionLeukocytesLong-Term EffectsLungMalignant NeoplasmsMalignant neoplasm of prostateMediatingMedicineMetastatic Neoplasm to the BoneMetastatic Prostate CancerMusMyelogenousMyeloid Cell SuppressionMyeloid CellsMyeloid-derived suppressor cellsNK Cell ActivationNatural Killer CellsNeoplasm MetastasisOsteoblastsOsteocalcinOsteoclastsPalliative CarePathway interactionsPatientsPharmacologyPhenotypePhosphotransferasesProcessPrognosisProstateProstatic NeoplasmsProtein InhibitionReceptor SignalingResearchScientistServicesSignaling ProteinSiteSoldierSourceTestingToxicologyTransgenic MiceTreatment outcomeTreatment-Related CancerTumor Cell InvasionTumor Cell MigrationTumor ExpansionTumor PromotionVeteransWorkZoledronic Acidadaptive immunityanti-tumor immune responsebasebonebone cellbone sialoproteincancer diagnosiscell typeeffective therapyexperimental studyfight againstimmune activationimmune functionimprovedin vivoinhibitor/antagonistmacrophagemelanomamimicrymortalitymouse modelneoplasm registryneoplastic cellnovelnovel therapeutic interventionpre-clinicalpreventprostate cancer cellprostate cancer metastasispublic health relevancerestorationskeletalsmall moleculestandard of caretargeted treatmenttumortumorigenic

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 DESCRIPTION (provided by applicant): Cancer and subsequent metastatic disease continue to be a significant source of mortality. Treatment and outcome are largely determined by whether the cancer has disseminated or metastasized, and once the cancer is no longer locally confined, patient prognosis is poor. We have few treatment opportunities for patients once they have metastases, typically resulting in palliative care. This project aims to study the Bone Morphogenetic Protein (BMP) pathway in metastatic prostate cancers, which preliminary data indicates may be a target for therapy and could potentially revolutionize the management of metastatic disease. This proposal focuses on three key areas: 1) Skeletal metastases, which may be dependent upon BMP signaling to persist. 2) Myeloid cell suppression of anti-tumor immune responses, which may be BMP dependent. 3) Restoration of the adaptive immune system to kill tumor cells through targeting in vivo the myeloid immune suppressive cells BMP signaling. Use of small molecule BMP antagonists developed by VA scientists originally for cardiovascular medicine may hold promise as novel treatments in the fight against metastatic cancers.
期刊论文(3)
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会议论文
DOI: 10.3390/cancers8110100
发表时间: 2016-11-04
期刊: Cancers
影响因子: 5.2
作者: [Jovanović B, Pickup MW, Chytil A, Gorska AE, Johnson KC, Moses HL, Owens P]
通讯作者: Owens P
Targeting the BMP pathway in metastatic cancer
Targeting the BMP pathway in metastatic cancer
  • 批准号:
    9141465
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    2016
  • 负责人:
    Philip Owens
  • 依托单位:
海外基金