Chemoprotectants for Head-Neck Therapeutics
Chemoprotectants for Head-Neck Therapeutics
批准号:
8326612
负责人:
HAICHING MA
金额:
$64.05万
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:
2011-09-01 至 2014-08-31
关键词:
AddressAdoptedAdverse effectsAffectAnimal ModelAnimal TestingApoptosisApoptosis RegulatorApoptoticBiological AssayBiological AvailabilityBiologyCaspaseCaspase InhibitorCell Cycle RegulationCell DeathCell LineCellsCessation of lifeCharacteristicsChemicalsChemoprotective AgentClinical TrialsCollaborationsComplicationCytoprotectionCytoprotective AgentDNA DamageDeglutitionDevelopmentDoseDose-LimitingDrug Delivery SystemsEffectivenessEnvironmentExhibitsFibroblastsFunctional disorderFutureGene ExpressionGenesGenomeGoalsGrantHead and Neck CancerHead and neck structureHumanIn VitroInhibitory Concentration 50LeadLifeMalignant NeoplasmsMalignant neoplasm of larynxMetabolismMethodsModelingMucous body substanceMutationNormal CellOncogenesOne-Step dentin bonding systemOralOral mucous membrane structurePainPatientsPenetrationPeptidesPharmaceutical PreparationsPharmacologic SubstancePhasePreventionPropertyRadiationRadiation therapyRadioReactionReaction TimeResearchSignal TransductionSiteStagingStructure-Activity RelationshipTestingTherapeuticTimeTissuesToxic effectWorkabsorptionanalogbasecancer cellcancer therapycaspase-3chemotherapydrug discoveryimprovedin vitro Modelin vivoinhibitor/antagonistkeratinocytenoveloral mucositisphase 1 studyprogramsradiation effectresponsescaffoldsmall molecule
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Chemoprotectants for Head-Neck Therapeutics Oral mucositis occurs as a major dose-limiting and complicating side effect of chemotherapy, radiotherapy, or combined chemo/radiotherapy. It is considered the most significant complication of head and neck cancer therapy. Oral mucositis is accompanied by tremendous pain and can cause life threatening complications. Dysfunction in swallowing following laryngeal cancer therapy can be particularly debilitating. The development of chemoprotectants is the central goal of this proposal. In preliminary studies, Reaction Biology Corporation has discovered selective, reversible, small molecule caspase inhibitors, which have multiple advantages compared to the compounds in the clinical trials. For example, caspase inhibitors from many pharmaceutical companies' drug discovery programs have one of more of the following characteristics: irreversible, peptide-mimic, Pan-caspase inhibitor. In Phase I studies, these compounds are very active in cell based assays, demonstrated significant cell death prevention activities in chemical and radiation induced cell death in normal cell lines. In this Phase II application, we will continue to improve these inhibitors in potency and efficacy in cell based assays and DMPK profiles, to look for the final lead(s) in animal model tests. In this new proposal, the key aims are: 1) Structure-Activity Relationship (SAR) studies to improve caspase inhibitors' potency; 2) Define caspase inhibitors' treatment conditions in vitro in conjugation with chemotherapy and radiation treatments; 3) Test caspase inhibitors' tissue penetration and efficacy in protecting oral mucous cells from radiation therapy in 3D oral mucosa model.
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