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FASEB SRC on HDACs, Sirtuins and Reversible Acetylation in Signaling and Disease

FASEB SRC on HDACs, Sirtuins and Reversible Acetylation in Signaling and Disease
FASEB SRC 关于 HDAC、Sirtuins 以及信号传导和疾病中的可逆乙酰化
批准号:
8595760
负责人:
SCOTT W HIEBERT
金额:
$0.7万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-07-15 至 2014-06-30
关键词:
AcetylationAcetyltransferaseAgingAging-Related ProcessAmericanAnimal Disease ModelsAnimal ModelAreaBasic ScienceBiochemistryBiologicalBiological ProcessBiologyBromodomainCardiovascular DiseasesCell Cycle ProgressionCell Differentiation processCell physiologyCellsCellular biologyChargeChromatin StructureClinicalClinical InvestigatorClinical ResearchClinical TreatmentClinical TrialsCloningCollaborationsCommunitiesCountryDNA biosynthesisDataDevelopmentDiabetes MellitusDiseaseDockingDrug IndustryDrug TargetingEnsureEnzymesEuropeanEventFacultyFemaleFertilizationFingersFosteringFutureGene ExpressionGene Expression RegulationGene ProteinsGenerationsGenome StabilityGoalsHDAC1 geneHIV InfectionsHealthHeart HypertrophyHistonesHousingHumanIn VitroInternationalItalyKnowledgeLinkLondonLongevityLysineMalignant NeoplasmsMetabolic DiseasesMetabolismMethylationModificationMolecular BiologyMolecular Mechanisms of ActionMolecular StructureNeurodegenerative DisordersNeuromuscular DiseasesOralParticipantPathogenesisPathologyPathway interactionsPharmaceutical PreparationsPharmacologic SubstancePharmacologyPhosphorylationPhysiologyPlayPost-Translational Protein ProcessingProcessProtein AcetylationProteinsReaderRegulationResearchResearch PersonnelResveratrolRoleScientistSideSignal TransductionSirtuinsSiteSolid NeoplasmSpeedStem cellsStructureTestingTimeTranslational ResearchUbiquitinationUnderrepresented MinorityWomanabstractingbasecareercareer developmentdrug discoveryfightinggraduate studenthuman diseasein vivoinhibitor/antagonistinnovationinterestleukemia/lymphomameetingsnervous system disordernext generationnovelnovel therapeuticsposterspreclinical studypreventprogramsprotein functionpublic health relevancered wineresearch clinical testingsmall moleculesocialsoundsymposiumtherapeutic targetyeast genetics

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中文摘要
翻译
描述(由申请人提供):组蛋白去乙酰化酶(hdac)是基本细胞事件的重要调节因子,包括细胞周期进程、干细胞功能、细胞命运决定、细胞分化和许多疾病的发病机制。因此,毫不奇怪,蛋白质乙酰化是人类疾病的核心,如神经退行性疾病、心脏肥厚、癌症、艾滋病毒感染,以及更普遍的衰老过程。更重要的是,小分子HDAC抑制剂和激活剂目前正在临床试验中,用于治疗白血病和淋巴瘤、实体瘤、神经肌肉疾病、代谢紊乱等疾病。此外,hdac的一个亚类Sirtuins在酵母基因研究中被指出可以调节寿命,这些酶可能是白藜芦醇的目标,白藜芦醇是红酒中与人类寿命延长有关的成分之一。因此,深入了解hdac是必要的,不仅是为了了解染色质结构、基因调控和蛋白质功能的调控,而且因为hdac密切参与对人类健康产生重大影响的正常和异常细胞过程。在过去的十年中,随着18种人类hdac (HDAC1- 11和SIRT1-7)和许多乙酰转移酶的鉴定、分离、克隆和功能表征,未来几年我们对hdac和蛋白质乙酰化的生物学作用的认识将继续急剧扩大。作为唯一一个专门针对该领域的会议,这个两年一次的会议在汇集约44位基础和临床科学家演讲者与来自世界各地的约120名参与者交流信息和开发新的治疗途径方面发挥着重要作用。主要目标是在基础学术研究人员、临床科学家和制药科学家之间转移知识,以提高效率,了解他们如何控制人类健康,以及如何利用这些活动来对抗各种疾病。第二个目标是培养年轻研究者的发展和兴趣,以帮助支持他们的职业发展。为了实现这些目标,会议场地包括会议空间、餐厅和房间,这样参与者就有足够的时间从正式的演讲转移到非正式的头脑风暴和协作讨论。此外,上午和晚上的口头报告环节包括从提交的摘要中选出的初级科学家的2-3次演讲,这对职业发展和鼓励下一代HDAC科学家非常重要。将通过科学和社会项目强调创建一个全球性的HDAC社区。这次会议将特别及时,因为将介绍新一代HDAC和Bromodomain药物的数据。因此,将于2013年8月18日至23日与FASEB联合在意大利卢卡的Il Ciocco举行的关于hdac和Sirtuins的生物学和治疗靶向及其在衰老和疾病中的作用的第4届双年度会议将获得支持。
英文摘要
DESCRIPTION (provided by applicant): Histone deacetylases (HDACs) are vital regulators of fundamental cellular events, including cell cycle progression, stem cell functions, cell fate determination, cell differentiation, and the pathogenesis of many diseases. As such, it is not surprising that protein acetylation is central to human diseases, as diverse as neurodegenerative disorders, cardiac hypertrophy, cancer, HIV infection, and more generally the process of aging. More importantly, small molecule HDAC inhibitors and activators are currently in clinical trials for the treatment of leukemia and lymphoma, solid tumors, neuromuscular disorders, metabolic disorders and other diseases. In addition, the Sirtuins, a subclass of HDACs, were fingered in yeast genetic studies as regulating lifespan, and these enzymes might be targeted by resveratrol, one of the components in red wine that has been linked to increased lifespan in humans. Therefore, a thorough understanding of HDACs is required, not merely for understanding the regulation of chromatin structure, gene regulation and protein function, but also because HDACs are intimately involved in normal and abnormal cellular processes that greatly impact human health. With the identification, isolation, cloning and functional characterization of 18 human HDACs (HDAC1- 11 and SIRT1-7) and many acetyltransferases in the past decade, the coming years will see a continued dramatic expansion in our knowledge of the biological roles of HDACs and protein acetylation. As the only conference dedicated to this field, this biannual meeting plays an essential role in bringing together approximately 44 basic and clinical scientist speakers to exchange information and develop new therapeutic avenues with approximately 120 participants from around the world. A primary objective is to transfer knowledge between basic academic researchers, clinical scientists, and pharmaceutical scientists to create efficiencies in understanding how they control human health and how these activities can be harnessed to fight a diverse slate of diseases. A second objective is to foster the development and interests of younger investigators to help support their career development. To accomplish these objectives, the meeting venue houses meeting space, dining, and rooms so that participants have ample time to move from formal presentations to informal brainstorming and collaborative discussions. In addition, the morning and evening oral presentation sessions include 2-3 talks from junior scientists selected from the submitted abstracts, which is important for career development and to encourage the next generation of HDAC scientists. There will be an emphasis through both the scientific and social programs on creating a global HDAC community. This meeting will be particularly timely because data from on a new generation of HDAC and Bromodomain drugs will be presented. Therefore, support is requested for the 4th biannual conference on the biology and therapeutic targeting of HDACs and Sirtuins, and their role in aging and disease to be held at Il Ciocco, Lucca, Italy, August 18-23, 2013 in conjunction with FASEB.
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会议论文
Role of PRC1 in RUNX1-ETO-mediated transcriptional control
  • 批准号:
    10445091
  • 项目类别:
  • 资助金额:
    $42.29万
  • 财政年份:
    2021
  • 负责人:
    SCOTT W HIEBERT
  • 依托单位:
Role of PRC1 in RUNX1-ETO-mediated transcriptional control
  • 批准号:
    10298288
  • 项目类别:
  • 资助金额:
    $45.72万
  • 财政年份:
    2021
  • 负责人:
    SCOTT W HIEBERT
  • 依托单位:
Role of PRC1 in RUNX1-ETO-mediated transcriptional control
  • 批准号:
    10652591
  • 项目类别:
  • 资助金额:
    $42.26万
  • 财政年份:
    2021
  • 负责人:
    SCOTT W HIEBERT
  • 依托单位:
Regulation of transcription and tumor suppression by MTG family members
  • 批准号:
    8696545
  • 项目类别:
  • 资助金额:
    $36.36万
  • 财政年份:
    2014
  • 负责人:
    SCOTT W HIEBERT
  • 依托单位:
海外基金