Genomic and Epigenomic Profiling by MSNP
Genomic and Epigenomic Profiling by MSNP
批准号:
7459086
负责人:
Benjamin Tycko
金额:
$24.15万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-07-01 至 2010-06-30
关键词:
AllelesAsiaBiologicalBiological AssayBiological ModelsCancerousCellsChromatinCompatibleCpG dinucleotideDNADNA MethylationDNA Microarray ChipDNA Microarray formatDNA SequenceDNA copy numberDataData AnalysesData ElementDetectionDigestionDiseaseEnsureEpigenetic ProcessEuropeFlow CytometryFundingGene ExpressionGene FrequencyGeneticGenomeGenomicsHumanHuman GenomeLightLoss of HeterozygosityMalignant NeoplasmsMapsMedicalMethodsMethylationMicrodissectionModificationMutationNephroblastomaNumbersPathogenesisPatternPilot ProjectsPolymerase Chain ReactionPopulationProto-OncogenesRecurrenceResolutionRunningSamplingScoreSingle Nucleotide PolymorphismSouthern BlottingStandards of Weights and MeasuresTechnologyTestingThinkingTissuesTumor Suppressor GenesWorkbisulfitecancer Biomedical Informatics Gridcancer cellcancer diagnosischromosome losscostdesignepigenomicshuman tissuemRNA Expressionneoplasticnovel strategiestechnology developmenttool
中文摘要
描述(由申请人提供):DNA甲基化改变是癌细胞的标志,表观遗传畸变包括DNA甲基化的获得和损失也是其他医学疾病的基础。这种表观遗传畸变被认为在癌症的发生和发展过程中与遗传变化(如染色体的丧失和获得)协同作用。在这项技术开发项目中,我们将开发并广泛验证一种具有成本效益,高分辨率和高通量的方法,用于同时表征人类癌症中DNA甲基化基因组的遗传畸变和改变。我们期望这种方法,我们缩写为MSNP(甲基化敏感SNP阵列分析),将有助于回答DNA序列与其甲基化模式(遗传/表观遗传相互作用和等位基因特异性DNA甲基化)之间的关系以及DNA甲基化与基因表达之间的关系等基本问题。以及实现重要的医学目标,包括识别由DNA甲基化调节的肿瘤抑制基因和原癌基因,以及发现用于癌症诊断和检测的新的强大标记。DNA甲基化改变是癌细胞的标志,DNA甲基化的获得和损失也是其他医学疾病的基础。该项目旨在优化和验证一种名为MSNP的新方法,用于在正常和癌变人体组织中以高分辨率检测和绘制整个人类基因组中的DNA甲基化。来自MSNP的数据有望揭示癌症的发病机制,并为癌症诊断和检测提供新的、强大的标志物。
英文摘要
DESCRIPTION (provided by applicant): Altered DNA methylation is a hallmark of cancer cells, and epigenetic aberrations including gains and losses of DNA methylation also underlie other medical disorders. Such epigenetic aberrations are thought to act in concert with genetic changes, such as chromosome losses and gains, in cancer initiation and progression. In this technology development project we will develop and extensively validate a cost-effective, high-resolution and high-throughput method for simultaneously characterizing genetic aberrations and alterations in DNA methylation genome wide in human cancers. We expect that this method, which we abbreviate MSNP (Methylation-sensitive SNP array analysis), will be useful both for answering fundamental questions such as the relationship between the DNA sequence and its pattern of methylation (genetic/epigenetic interactions and allele-specific DNA methylation) and the relationship between DNA methylation and gene expression, and for achieving important medical objectives including identifying tumor suppressor genes and proto-oncogenes regulated by DNA methylation and finding new and robust markers for cancer diagnosis and detection. Altered DNA methylation is a hallmark of cancer cells, and gains and losses of DNA methylation also underlie other medical disorders. This project is designed to optimize and validate a new method, called MSNP, for detecting and mapping DNA methylation at high resolution across the entire human genome in both normal and cancerous human tissues. Data from MSNP are expected to shed light on cancer pathogenesis and produce new and robust markers for cancer diagnosis and detection.
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