Functional Assembly of Salivary Cells to Relieve Xerostomia
Functional Assembly of Salivary Cells to Relieve Xerostomia
批准号:
8390897
负责人:
MARY C FARACH-CARSON
金额:
$63.18万
依托单位:
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:
2012-07-17 至 2016-06-30
关键词:
Acinar CellAddressAdverse effectsAffectAgonistAnimal ModelArtificial SalivaAutologousBasement membraneBiocompatibleBiologicalBiological ProcessBlood VesselsBody Weight decreasedCell CommunicationCell SurvivalCellsChemicalsClinicalCollaborationsComplexCuesDeglutitionDentalDental cariesDifferentiation and GrowthDisease ProgressionDuctal Epithelial CellEatingEngineeringEnzymesEpithelial CellsEpitopesEthylene GlycolsExtracellular MatrixExtracellular Matrix ProteinsGelGlandGoalsGrowth FactorHead and Neck CancerHead and neck structureHumanHyaluronic AcidHybridsHydrogelsImmune responseImplantIn VitroIndividualInfectionInjuryIon ChannelLaboratoriesMechanicsMembrane ProteinsMethodsModelingModificationMorphogenesisMyoepithelial cellNatural regenerationOperative Surgical ProceduresOral cavityOrganPatientsPeptidesPerformancePhenotypePhysiologicalPopulationPreventionProductionPropertyQuality of lifeRadiationRadiation therapyRadiation-Protective AgentsRattusRecoveryRegenerative MedicineResearch PersonnelSalivaSalivarySalivary GlandsSignal TransductionSiteSolutionsStem cellsStimulusStructureSurgical OncologistSystemTechnologyTherapeuticTissue EngineeringTissue SampleTissuesTransplantationXerostomiaangiogenesisbasecell typecontrolled releasecopolymerdesignethylene glycolflexibilityfunctional restorationhuman tissueimplantationin vivoin vivo Modelnovelparticleperlecanphysical propertyprogenitorprototypereconstitutionresponserestorationsaliva secretionsalivary acinar cellsalivary cellscaffoldtissue regenerationwater channel
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Xerostomia, or 'dry mouth', is the inevitable consequence of the standard radiation treatment for head and neck cancers, and leads to severe dental issues (caries, infections, decay), difficulties in swallowing, speaking, and eating,
gradual weight loss, and overall discomfort. Current therapies have not proven effective in long term application, and few tissue engineering strategies have been applied to this problem. In this application, we assemble three PIs with the necessary engineering, biological, and clinical expertise to address salivary regeneration using core biological design principles. In Aim 1, Xinqiao Jia's laboratory will develop hyaluronic acid (HA) gels as a modular cellular scaffolding material. HA is a compelling material for salivary gland regenerative medicine, as it is naturally derived, biodegradable, and offers flexible tuning of chemical and mechanical properties to match those of native tissue. Microscale HA hydrogel particles (HGP) will be used as growth factor depots to stimulate salivary cell organization, gland morphogenesis, and vascular input to the neotissue. In Aim 2, Cindy Farach-Carson's laboratory will apply these technologies in vitro, leveraging their ability to reliably isolate and expand acinar, ductal, and myoepithelial cells fro human tissue samples. Bioactive fragments will be incorporated into the HA matrix to facilitate acinar/ductal cell organization, and cell reconstitution will be conducted in a stepwise fashion to
insure proper lumen formation, polarity, and function. In Aim 3, Robert Witt will conduct in vivo implantations of HA matrices in an animal model, to determine the host response to the HGP growth factors, the viability of the neo-salivary glands, and a functional assessment of saliva production, content, and quality. These three Aims combine fresh discoveries from an existing collaboration among the three PIs, and maintain a clear goal of eventual translational application.
PUBLIC HEALTH RELEVANCE: Patients with cancers of the head and neck often undergo radiation therapy as a part of their initial treatment. One side-effect of this radiation is atroph of cells in the mouth that produce saliva, which leads to xerostomia or 'dry mouth'. Xerostomia markedly lowers quality of life. We have identified methods for isolating these cells prior to radiation, growing them in the lab, and seeding them within gels that could help the cells reform as functional salivary glands, which could then be returned to the original patient.
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会议论文
Functional Biointegration of Bioengineered Salivary Tissues in Irradiated Animal Models
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批准号:10706557
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项目类别:
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资助金额:$68.03万
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财政年份:2022
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负责人:MARY C FARACH-CARSON
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依托单位:
Functional Biointegration of Bioengineered Salivary Tissues in Irradiated Animal Models
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批准号:10569404
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项目类别:
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资助金额:$72.76万
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财政年份:2022
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负责人:MARY C FARACH-CARSON
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依托单位:
Cell-Based Therapy in Minipig Model of Radiation-Induced Xerostomia
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批准号:10214978
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项目类别:
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资助金额:$40.45万
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财政年份:2020
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负责人:MARY C FARACH-CARSON
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依托单位:
Supplement to R01 Titled: Mechanosensing in the Bone Lacunar-Canalicular System
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批准号:9298122
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项目类别:
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资助金额:$6.49万
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财政年份:2016
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负责人:MARY C FARACH-CARSON
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依托单位:
Functional Assembly of Salivary Cells to Relieve Xerostomia
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批准号:8512701
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项目类别:
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资助金额:$57.77万
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财政年份:2012
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负责人:MARY C FARACH-CARSON
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依托单位:
Functional Assembly of Salivary Cells to Relieve Xerostomia
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批准号:8878217
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项目类别:
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资助金额:$60.18万
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财政年份:2012
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负责人:MARY C FARACH-CARSON
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依托单位:
Functional Assembly of Salivary Cells to Relieve Xerostomia
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批准号:8815356
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项目类别:
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资助金额:$2.57万
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财政年份:2012
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负责人:MARY C FARACH-CARSON
-
依托单位:
Functional Assembly of Salivary Cells to Relieve Xerostomia
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批准号:8668772
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项目类别:
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资助金额:$66.61万
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财政年份:2012
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负责人:MARY C FARACH-CARSON
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依托单位:
PERLECAN AND HEPARANASE IN CARTILAGE GROWTH AND HEALING
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批准号:7959490
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项目类别:
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资助金额:$31.59万
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财政年份:2009
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负责人:MARY C FARACH-CARSON
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依托单位:
ELECTROSPUN COLLAGEN SCAFFOLDS FOR 3D CELLULAR MODELS FOR ANTI-NEOPLASTIC AGENTS
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批准号:7960178
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项目类别:
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资助金额:$5.46万
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财政年份:2009
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负责人:MARY C FARACH-CARSON
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依托单位:
PERLECAN AND HEPARANASE IN CARTILAGE GROWTH AND HEALING
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批准号:7720203
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项目类别:
-
资助金额:$33.01万
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财政年份:2008
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负责人:MARY C FARACH-CARSON
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依托单位:
ELECTROSPUN COLLAGEN SCAFFOLDS FOR 3D CELLULAR MODELS FOR ANTI-NEOPLASTIC AGENTS
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批准号:7720256
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项目类别:
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资助金额:$4.41万
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财政年份:2008
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负责人:MARY C FARACH-CARSON
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依托单位:
Heparan Sulfate Proteoglycans in Bone Stromal Metastasis
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批准号:8382407
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项目类别:
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资助金额:$36.83万
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财政年份:2003
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负责人:MARY C FARACH-CARSON
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依托单位:
Heparan Sulfate Proteoglycans in Bone Stromal Metastasis
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批准号:8305765
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项目类别:
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资助金额:$36.94万
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财政年份:2003
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负责人:MARY C FARACH-CARSON
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依托单位:
Project 2: Heparan Sulfate Proteoglycans in Prostate Cancer Bone Metastasis
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批准号:8794375
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项目类别:
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资助金额:$30.98万
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财政年份:2003
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负责人:MARY C FARACH-CARSON
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依托单位:
Heparan Sulfate Proteoglycans in Bone Stromal Metastasis
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批准号:7617319
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项目类别:
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资助金额:$40.44万
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财政年份:2003
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负责人:MARY C FARACH-CARSON
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依托单位:
Heparan Sulfate Proteoglycans in Bone Stromal Metastasis
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批准号:8112667
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项目类别:
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资助金额:$38.14万
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财政年份:2003
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负责人:MARY C FARACH-CARSON
-
依托单位:
Project 2: Heparan Sulfate Proteoglycans in Prostate Cancer Bone Metastasis
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批准号:9149383
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项目类别:
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资助金额:$30.79万
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财政年份:2003
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负责人:MARY C FARACH-CARSON
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依托单位:
Heparan Sulfate Proteoglycans in Bone Stromal Metastasis
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批准号:8528347
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项目类别:
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资助金额:$35.19万
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财政年份:2003
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负责人:MARY C FARACH-CARSON
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依托单位:
REGULATION OF CALCIUM CHANNEL EXPRESSION IN OSTEOBLASTS
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批准号:6379847
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项目类别:
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资助金额:$25.9万
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财政年份:1999
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负责人:MARY C FARACH-CARSON
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依托单位:
海外基金