Human Apyrase to Disrupt Cancer Therapy
Human Apyrase to Disrupt Cancer Therapy
批准号:
7599772
负责人:
RIDONG CHEN
金额:
$19.67万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-09-12 至 2010-09-11
关键词:
AdhesionsAntiplatelet DrugsApyraseAspirinBiological AssayBleeding time procedureBloodBlood PlateletsBlood VesselsBody WeightBone PainBreastCancer PatientCause of DeathCell LineCell surfaceCellsCessation of lifeChinese Hamster Ovary CellClinicClinicalColorectal AdenomaColorectal CancerComputer AssistedCulture MediaCytotoxic ChemotherapyDiagnosisDiseaseDoseEndothelial CellsEndotheliumEndotoxinsEngineeringEnzymesExhibitsFatty acid glycerol estersFundingGenerationsGenesGliomaGoalsGrantGrowthGuanosine MonophosphateHalf-LifeHemorrhageHistologicHormone ReceptorHumanHydrolysisImmunocompetentIn VitroIncidenceInformaticsInvasiveLaboratoriesLeadLifeLuciferasesLungMalignant NeoplasmsMalignant neoplasm of prostateMammalian CellMammary glandMetastatic Neoplasm to the BoneModelingMusNeoplasm MetastasisOralOutcomePathway interactionsPatientsPharmaceutical PreparationsPhasePlatelet ActivationPlatelet Glycoprotein GPIIb-IIIa ComplexPlatelet aggregationPreclinical TestingPreventionProductionProphylactic treatmentProteinsPublic HealthRattusResearchRiskSafetySerumSubcutaneous InjectionsSystemTailTestingTimeTreatment ProtocolsTumor BurdenTumor-DerivedUnited StatesUniversitiesVeinsWashingtonadenomaaging populationcancer cellcancer therapyclinically relevantdayextracellularfluidityimprovedin vivoinhibitor/antagonistmalignant breast neoplasmmedical schoolsneoplastic cellnovelnovel therapeuticstherapeutic proteinvector
中文摘要
描述(申请人提供):人apyrase代表了一种非常有希望的抑制癌症转移的治疗方法。这种酶强烈抑制血小板的激活和聚集,而不会增加出血的风险。利用蛋白质信息学的方法,我们成功地设计了一个优化的人类apyrase,APT102。有了第一阶段的支持,我们将确定APT102单独或与阿司匹林联合使用在抑制小鼠实验性自发转移方面是有效的。公共卫生相关性:人类apyrase代表了一种非常有希望的癌症治疗方法。我们将确定靶向apyrase单独或与阿司匹林联合使用是否能有效抑制小鼠的实验性转移。
英文摘要
DESCRIPTION (provided by applicant): Human apyrase represents a highly promising therapy for inhibition of cancer metastasis. The enzyme strongly inhibits platelet activation and aggregation without increasing bleeding risk. Using a protein informatics approach, we have successfully engineered an optimized human apyrase, APT102. With the Phase I grant support, we will determine whether APT102, alone or in combination with aspirin, is effective in inhibiting experimental spontaneous metastasis in mice. PUBLIC HEALTH RELEVANCE:Human apyrase represents a highly promising therapy for cancer treatment. We will determine whether the targeted apyrase, alone or in combination with aspirin, is effective in inhibiting experimental metastasis in mice.
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