Enhancing Viral Oncolysis with Vasculostatin Gene Delivery
Enhancing Viral Oncolysis with Vasculostatin Gene Delivery
批准号:
8638899
负责人:
Balveen Kaur
金额:
$39.51万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-04-01 至 2016-03-31
关键词:
American Cancer SocietyAngiogenesis InhibitorsAngiostatic ProteinsAnimal ModelApoptoticBindingBiologyBrainBrain NeoplasmsCellsCessation of lifeClinical TrialsCytolysisDevelopmentDominant-Negative MutationEatingExtracellular DomainGene DeliveryGene ExpressionGenesGliomaGoalsGrantHerpesvirus 1HypoxiaIn VitroLaboratoriesLeadLengthMalignant GliomaMalignant NeoplasmsModalityMusOncolyticOncolytic virusesPatientsPerfusionPhagocytosisPhosphatidylserinesPlayPropertyResearchRoleSignal TransductionSimplexvirusStructureTestingTherapeuticTissuesToxic effectTranslatingTumor BiologyVasculostatinViralVirusVirus Replicationangiogenesisarmbasecancer celldensityexpectationextracellularfootin vivokillingsmacrophagenestin proteinoncolysisoutcome forecastpreclinical toxicitypublic health relevancereceptorresponsetumortumor microenvironmenttumorigenic
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The ultimate goal of this proposal is to understand the contribution of Vstat120 expressing oncolytic viruses on OV propagation, tumor biology and anti-tumor efficacy. These results will lead to a better understanding of OV therapy induced changes in tumor biology and will lead to the development of a dually armed cancer killing OV. The OV treatment of tumors relies on cancer-specific replication of the virus leading to tumor destruction with minimal toxicity to adjacent non-neoplastic tissue. Results from six clinical trials using replication competent OVs to treat patients with malignant glioma have shown the new modality to be relatively safe, but high expectations of efficacy remain unmet (1, 2). The tumor's microenvironment is increasingly recognized as an important determinant for its progression and its response to therapeutics. My laboratory has recently created two oncolytic viruses, armed with an anti-angiogenic gene. We now propose to elucidate the role of this angiostatic protein in viral propagation, glioma biology and OV efficacy.
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海外基金