Nuclear Receptors: Full Throttle
Nuclear Receptors: Full Throttle
批准号:
8985996
负责人:
DAVID L. WOODLAND
金额:
$0.6万
依托单位:
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:
2016-01-01 至 2016-12-31
关键词:
AcademiaAddressAdverse effectsAreaBindingBiologyCancer EtiologyCardiovascular DiseasesCessation of lifeCholestasisChromatin StructureClinicalCollaborationsComplexConflict (Psychology)DataDevelopmentDiabetes MellitusDietary FatsDisciplineDiseaseDrug TargetingEducational workshopEmerging TechnologiesEndocrine System DiseasesFamilyFatty acid glycerol estersFertilizationFutureGene Expression RegulationGeneticGenetic TranscriptionGenomeHealthHomeostasisHormonesHumanHypertensionImmune systemIndustryInflammationJointsKnowledgeLearningLigandsLongevityMalignant NeoplasmsMalignant neoplasm of lungMalignant neoplasm of prostateMembraneMetabolic DiseasesMetabolismMethodologyModelingMolecularNuclearNuclear ReceptorsObesityOutcomePharmacologic SubstancePhysiologicalPhysiologyPlayProcessProteomeQuality of lifeRegulator GenesReproductionResearchResearch PersonnelRoleScienceScientistSenior ScientistSignal PathwaySignal TransductionSpeedTissuesTranslationsUtahVitaminsWomanWorkadvanced diseasecareerclinical practicecombinatorialdrug developmentimmune functionimprovedinnovative technologiesinsightinterestmalignant breast neoplasmmeetingsmenneoplasticnew technologynext generationnon-genomicnovelnovel strategiesposterspreventprogramspublic health relevancereceptorreceptor functionresistance mechanismresponsesensorsteroid hormone receptorsymposiumtherapy resistanttranscription factor
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Support is requested for a Keystone Symposia meeting entitled Nuclear Receptors: Full Throttle, organized by Carol A. Lange, Jennifer K. Richer and Karen E. Knudsen. The meeting will be held in Snowbird, Utah from January 10-15, 2016. Nuclear receptors (NRs) represent a large superfamily of ligand-dependent transcription factor "sensors" for a diverse set of fat-soluble hormones, vitamins and dietary lipids. NRs orchestrate genetic response programs critical for normal homeostasis, and are required for reproduction, development, metabolism and immune function. For this reason, NRs have been investigated for over 30 years as promising targets for drugs to treat a broad spectrum of diseases including cancer, diabetes and other endocrine or metabolic disorders, obesity, cardiovascular disease, hypertension, inflammation and cholestasis. Research on NRs has led to numerous successful therapies for deadly diseases that have improved both longevity and quality of life. However, significant hurdles remain that involve further detailed understanding of
the major gene regulatory networks regulated by NRs, how these differ in normal relative to pre-disease and disease states, and the complex problems associated with targeting tissue-specific effects (to reduce side effects) and circumventing mechanisms of resistance. Thus, further insight into the full range of NR functions and interactions with co-regulatory molecules and signaling pathways is necessary for combinatorial approaches involving NRs in health and disease, and development of next-generation therapies. This meeting will bring together a diverse array of our leading scientists, including senior and junior investigators and their trainees, from academic, clinical and pharmaceutical settings, to showcase the latest science, highlight the use of innovative and emerging technologies, explore new directions, and develop collaborative and synergistic efforts in the exciting field of NR biology.
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