eDyNAmiC - NYU
eDynamic - 纽约大学
基本信息
- 批准号:10845757
- 负责人:
- 金额:$ 31.82万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2022
- 资助国家:美国
- 起止时间:2022-06-24 至 2024-05-31
- 项目状态:已结题
- 来源:
- 关键词:AccelerationAdvocateAffectArchitectureBloodCancer PatientCellsChemicalsChemistryChromosome PairingChromosomesCollaborationsCommunitiesComputersDNADataDiagnosticDrug TargetingDrug resistanceEarly DiagnosisEducationEvolutionFamilyFingerprintFosteringFunding MechanismsGene Expression RegulationGene OrderGenerationsGenesGeneticGenetic TranscriptionGenomeHumanImmune EvasionImmune systemImmunobiologyImmunologicsImmunologyImmunotherapyInfrastructureInternationalLicensingLigandsMaintenanceMalignant NeoplasmsMedicineModelingMonitorMutationNucleic AcidsOncogenesPatientsPharmaceutical PreparationsProcessProductivityResearch PersonnelResourcesRoleScientistTherapeuticTissuesTumor PromotionWorkYeast Model Systemcancer genomicscancer heterogeneitycancer typecombinatorialepigenomicsexperienceextrachromosomal DNAgenome sequencinginnovationinsightlive cell imagingmachine learning algorithmmathematical modelmultiple omicsnovelpreventprogramstime usetooltumortumor growthwhole genomeyeast genetics
项目摘要
eDyNAmiC (extrachromosomal DNA in Cancer)
Human genes are arranged on 23 pairs of chromosomes, but in cancer, tumour-promoting genes can free themselves from chromosomes and relocate to circular, extrachromosomal pieces of DNA (ecDNA). These ecDNA do not follow the normal “rules” of chromosomal inheritance, enabling tumours to achieve far higher levels of cancer-causing oncogenes than would otherwise be possible, and licensing cancers with a way to evolve and change their genomes to evade treatments at rates that would be unthinkable for human cells. The altered circular architecture of ecDNAs also changes the way that the cancer-causing genes are regulated and expressed, further contributing to aggressive tumour growth. These unique features make ecDNA-containing cancers especially aggressive and difficult to treat. Cancer patients whose tumours harbour ecDNA have markedly shorter survival. Despite being first seen over fifty years ago, the critical importance of ecDNA has only recently come to light, and the scale of the problem is substantial. ecDNAs are present in nearly half of all human cancer types and potentially up-to a third of all cancer patients. The collective current understanding of how ecDNA form, how they function, how they move around the cell, how they evolve to resist treatment, how they impact the immune system, and how they can be effectively targeted are lacking. We bring together an internationally recognized, pioneering interdisciplinary team of cancer biologists, geneticists, computer scientists, evolutionary biologists, mathematicians, clinicians, and patient advocates to boldly create novel insights and resources and to provide transformative solutions to one of Cancer’s Grand Challenges. A core team of experienced and productive ecDNA investigators will work with new investigators in the ecDNA and cancer fields to bring completely new perspectives and approaches to this daunting challenge. By bridging cutting-edge and diverse approaches and insights from cancer genomics, yeast genetics, epigenomics, artificial genome synthesis, longitudinal patient tracking, combinatorial and machine learning algorithms, mathematical modelling, immunobiology, and innovative chemistry we will develop a new understanding of the role of ecDNA in cancer, and we will find new ways to drug the undruggable. This bold programme, which consists of 7 work packages and a committed international infrastructure, generates new and unusual collaborations that would simply be impossible under any other type of funding mechanism. Our programme endeavours to foster bold innovative solutions to one of the hardest problems in cancer and to one of the greatest challenges facing cancer patients.
癌症染色体外DNA研究
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Jef D BOEKE其他文献
Jef D BOEKE的其他文献
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{{ truncateString('Jef D BOEKE', 18)}}的其他基金
MutSensor System: A Set of Highly Sensitive Mutation Reporters to Dissect Genome Stability in Health and Disease
MutSensor 系统:一组高度灵敏的突变报告基因,用于剖析健康和疾病中基因组的稳定性
- 批准号:
10737167 - 财政年份:2023
- 资助金额:
$ 31.82万 - 项目类别:
Brca1-Mediated Suppression Of Retrotransposon Activity - Resubmission - 1
Brca1 介导的逆转录转座子活性抑制 - 重新提交 - 1
- 批准号:
9979202 - 财政年份:2020
- 资助金额:
$ 31.82万 - 项目类别:
Supplement for Center for Synthetic Regulatory Genomics: Building CACNA1C alleles associated with Neuropsychiatric Disorders
合成调控基因组学中心的补充:构建与神经精神疾病相关的 CACNA1C 等位基因
- 批准号:
10405299 - 财政年份:2018
- 资助金额:
$ 31.82万 - 项目类别:
CEGS: Center for Synthetic Regulatory Genomics - Renewal
CEGS:合成监管基因组学中心 - 更新
- 批准号:
10652025 - 财政年份:2018
- 资助金额:
$ 31.82万 - 项目类别:
Core B - Retrotransposon Genomics, Technology and Analysis Core
核心 B - 逆转录转座子基因组学、技术和分析核心
- 批准号:
10581511 - 财政年份:2016
- 资助金额:
$ 31.82万 - 项目类别:
Core B - Retrotransposon Genomics, Technology and Analysis Core
核心 B - 逆转录转座子基因组学、技术和分析核心
- 批准号:
10333659 - 财政年份:2016
- 资助金额:
$ 31.82万 - 项目类别:
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