Role of epigenetic regulators in pancreatic cancer
Role of epigenetic regulators in pancreatic cancer
批准号:
8093877
负责人:
Alexandros Tzatsos
金额:
$14.99万
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:
2011-09-16 至 2013-08-31
关键词:
AddressAdenocarcinoma CellBenchmarkingBiochemicalBiologicalBiological ProcessBiologyCDKN2A geneCancer EtiologyCell LineCellsCessation of lifeChromatinCodeComplexCoupledDevelopmentEZH2 geneEngineeringEnzymesEpigenetic ProcessFamilyFutureGene Expression ProfilingGene MutationGene SilencingGene TargetingGenesGenetic ScreeningGenetic TranscriptionGenetically Engineered MouseGlobal ChangeGrowthHistonesIn VitroKRAS2 geneKnockout MiceLesionLightMADH4 geneMaintenanceMalignant NeoplasmsMalignant neoplasm of pancreasMapsMediatingMediator of activation proteinMethylationMicroRNAsModelingMolecularMutationOncogenicPancreasPancreatic Ductal AdenocarcinomaPathogenesisPatternPlayPolycombPremalignantPrevalencePrimary Cell CulturesProcessProteinsRegulationRepressionRoleShapesStem cellsSystemTherapeuticTransgenic OrganismsTumor Suppressor ProteinsTumorigenicityUndifferentiatedUnited StatesUp-RegulationWorkbasecancer stem cellchromatin modificationclinically relevantdemethylationembryonic stem cellgene repressiongenetic regulatory proteingenome-widehistone methyltransferasehistone modificationin vivoinduced pluripotent stem cellinhibitor/antagonistloss of functionmouse modelneoplastic cellnovelnovel strategiesnovel therapeuticspluripotencypressureprogramspromoterself-renewalsenescencesmall hairpin RNAsmall moleculetherapeutic targettumor growthtumor progression
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Eukaryotic gene transcription is influenced by chromatin modifications that are under the control of epigenetic regulatory proteins. In addition to genetic alterations, it is now apparent that epigenetic mechanisms are also central to cancer pathogenesis. Epigenetic alterations are heritable, drive neoplastic progression, and undergo the same selective pressure as genetic alterations. Therefore identifying the key epigenetic regulators in cancers should point to new and better therapeutic approaches. An integrative biology approach has been employed to identify and dissect the role that families of histone modifying enzymes play in the development of pancreatic ductal adenocarcinoma (PDAC), the 4th most common cause of cancer death in the United States. This unbiased genetic screen led the discovery of the family of jumonji-domain histone demethylases (HDMs) as important regulators of PDAC. In particular, it has been found that the HDM, KDM2B, was highly upregulated in PDAC and was required for the tumorigenicity of PDAC cell lines and the immortalization and transformation of primary cells. By using gain- and loss-of-function approaches and genetically engineered mouse models we propose to delineate the molecular mechanisms by which KDM2B contributes to PDAC initiation, progression, and maintenance by defining key target genes and establishing the functional interaction between KDM2B and other chromatin modifying enzymes. Given the reversibility of histone methylation and the importance of the Jumonji domain, KDM2B -unlike many other oncogenic transcriptional regulators- represents an attractive candidate for the development of small molecule inhibitors.
PUBLIC HEALTH RELEVANCE: In addition to genetic alterations, epigenetic mechanisms are also central to cancer pathogenesis. Epigenetic alterations are heritable, drive neoplastic progression, and undergo the same selective pressure as genetic alterations. Identifying the key epigenetic regulators in cancer should point to new and better therapeutic approaches.
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依托单位:
海外基金