Targeting the Circadian Rhythm in Glioblastoma Stem Cells (R01CA238662)
靶向胶质母细胞瘤干细胞的昼夜节律 (R01CA238662)
基本信息
- 批准号:10419142
- 负责人:
- 金额:$ 46.33万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2021
- 资助国家:美国
- 起止时间:2021-07-01 至 2024-11-30
- 项目状态:已结题
- 来源:
- 关键词:ARNTL geneAdjuvantAdoptedAgeAgonistAlpha RhythmAngiogenic FactorApoptosisAttenuatedBindingBiological ClocksBrainBrain NeoplasmsCarbonCaringCell Cycle ArrestCell MaintenanceCellsCellular Metabolic ProcessChemoresistanceChromatinCircadian RhythmsCitric Acid CycleClinicalCombined Modality TherapyComplexCytolysisDNA DamageDataDependenceDevelopmentDown-RegulationEnzymesEvolutionExcisionExposure toFeedbackFoundationsGenesGenetic TranscriptionGlioblastomaGliomaGlucoseHourHumanImmuneIn VitroInvadedIonizing radiationMaintenanceMalignant - descriptorMalignant NeoplasmsMediatingMetabolicMetabolic PathwayMetabolismMitochondriaMolecularNeuronsNormal CellOncogenicOperative Surgical ProceduresOralOrganismPathway interactionsPatientsPerformance StatusPlanet EarthPlanetsPrognosisProteinsRadiation therapyRecurrenceRegulationRegulatory PathwayReportingResearch Project GrantsResistanceRespirationRoleRotationSignal Transduction PathwayTestingToxic effectTranslatingTreatment FailureTricarboxylic Acidsangiogenesisbasecancer stem cellcell growthchemotherapychromatin immunoprecipitationcircadiancircadian pacemakerclinically significantconventional therapycryptochromedesigneffective therapyempoweredepigenetic regulationimprovedneoplastic cellnerve stem cellnew therapeutic targetnovelnovel therapeuticspalliationpatient responsepatient stratificationpre-clinicalradiation resistanceresponseself-renewalsmall hairpin RNAsmall moleculesmall molecule inhibitorstemstem cell biologystem cell differentiationstem cell growthstem cell proliferationstem cell self renewalstem cellsstem-like cellstemnesstargeted agenttemozolomidetherapeutically effectivetherapy resistanttranscription factortumor
项目摘要
Glioblastomas rank among the most lethal of all human cancers. Current therapy includes maximal surgical
resection, followed by combined radiotherapy and oral chemotherapy (temozolomide), and adjuvant
temozolomide. Maximal current therapy offers only palliation. Median survival for glioblastoma patients has
been reported to be 15-21 months, but these data are derived from patients with favorable age and
performance status. Recurrent glioblastoma therapy is limited with little evidence for effective therapy.
Treatment failure is derived from numerous causes, including the presence of stem-like tumor cells, called
glioblastoma stem cells (GSCs). GSCs contribute to radioresistance, chemoresistance, invasion, immune
escape, and angiogenesis. GSCs display dependencies on specific signal transduction pathways and
epigenetic regulation, associated with metabolic reprogramming.
Almost all living organisms on earth are exposed to a regular 24-hour day-night cycles generated by planet’s
rotation around its own axis, which in return leads to the evolution of intrinsic, entrainable circadian rhythm
driven by cell autonomous biological clocks. Molecular oscillation of transcriptional circuitry to regulate
circadian rhythms include positive regulation by the BMAL1 and CLOCK transcription factors, with two
negative regulatory loops that either transcriptionally downregulate BMAL1 or bind and inhibit
BMAL1:CLOCK transcriptional complexes. In our proposed studies, we leverage preliminary findings that the
circadian rhythm machinery serves distinct cellular and molecular roles in maintenance of GSCs. We will
determine the necessity for circadian rhythm regulation in GSCs mediate through metabolic reprogramming
and selective activation of oncogenic pathways.
To translate these efforts into novel clinical paradigms, we are using a novel class of agents that target
circadian clock function. These small molecule inhibitors are brain penetrant and can be combined with other
therapies to create synergistic targeting of GSCs. To generate the most effective therapeutic paradigm, we
will interrogate the preclinical utility of novel targeted therapies that disrupt the circadian rhythm oscillatory
loop that could accentuate the efficacy of conventional therapy. Collectively, the proposed studies will lay
the foundation for improved understanding of circadian rhythm regulation in cancer stem cell biology with
possible application to improved oncologic care.
胶质母细胞瘤是所有人类癌症中最致命的。目前的治疗包括最大限度的手术
项目成果
期刊论文数量(0)
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STEVE A KAY其他文献
STEVE A KAY的其他文献
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{{ truncateString('STEVE A KAY', 18)}}的其他基金
Targeting the Circadian Rhythm in Glioblastoma Stem Cells (R01CA238662)
靶向胶质母细胞瘤干细胞的昼夜节律 (R01CA238662)
- 批准号:
10530615 - 财政年份:2021
- 资助金额:
$ 46.33万 - 项目类别:
Targeting the Circadian Rhythm in Glioblastoma Stem Cells (R01CA238662)
靶向胶质母细胞瘤干细胞的昼夜节律 (R01CA238662)
- 批准号:
10308040 - 财政年份:2021
- 资助金额:
$ 46.33万 - 项目类别:
Targeting the Circadian Rhythm in Glioblastoma Stem Cells
针对胶质母细胞瘤干细胞的昼夜节律
- 批准号:
9888132 - 财政年份:2019
- 资助金额:
$ 46.33万 - 项目类别:
Targeting the Circadian Rhythm in Glioblastoma Stem Cells
针对胶质母细胞瘤干细胞的昼夜节律
- 批准号:
10061578 - 财政年份:2019
- 资助金额:
$ 46.33万 - 项目类别:
The Role of Cryptochromes in Circadian Regulation of Metabolism
隐花色素在代谢昼夜节律调节中的作用
- 批准号:
9342896 - 财政年份:2016
- 资助金额:
$ 46.33万 - 项目类别:
The Role of Cryptochromes in Circadian Regulation of Metabolism
隐花色素在代谢昼夜节律调节中的作用
- 批准号:
9175163 - 财政年份:2016
- 资助金额:
$ 46.33万 - 项目类别:
Role of Ror proteins in the mammalian circadian clock
Ror 蛋白在哺乳动物生物钟中的作用
- 批准号:
7204152 - 财政年份:2006
- 资助金额:
$ 46.33万 - 项目类别:
Role of Ror proteins in the mammalian circadian clock
Ror 蛋白在哺乳动物生物钟中的作用
- 批准号:
8656526 - 财政年份:2006
- 资助金额:
$ 46.33万 - 项目类别:
Role of Ror proteins in the mammalian circadian clock
Ror 蛋白在哺乳动物生物钟中的作用
- 批准号:
7390286 - 财政年份:2006
- 资助金额:
$ 46.33万 - 项目类别:
Role of Ror proteins in the mammalian circadian clock
Ror 蛋白在哺乳动物生物钟中的作用
- 批准号:
8328724 - 财政年份:2006
- 资助金额:
$ 46.33万 - 项目类别:
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