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Cancer target discovery using SAGE.

机译:使用SAGE发现癌症靶标。

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摘要

Cancer is a genetic disease. Genetic events including mutations, chromosomal gains, losses and rearrangements, along with epigenetic alterations, lead to significant transcriptional changes in cancer cells. Changes in the expression of many genes associated with the onset and progression of cancer likely contribute to the cancerous phenotype. SAGE (Serial Analysis of Gene Expression) is an expression profiling method that allows for global, unbiased and quantitative characterisation of transcriptomes. The expression of thousands of genes can be analysed simultaneously without prior knowledge of their sequence, thus leading to the discovery of novel transcripts. In addition to characterising normal and malignant gene expression patterns, SAGE can be used to identify downstream targets of tumour suppressors and oncogenes and further annotate genomes. Comprehensive analyses of expression profiles using SAGE will yield many new diagnostic and prognostic markers as well as therapeutic targets in cancer.
机译:癌症是一种遗传疾病。包括突变,染色体获得,损失和重排在内的遗传事件,以及表观遗传学改变,都会导致癌细胞的显着转录变化。与癌症的发生和发展有关的许多基因的表达变化可能有助于癌表型。 SAGE(基因表达的序列分析)是一种表达谱分析方法,可对转录组进行全局,无偏和定量表征。无需事先了解其序列即可同时分析数千种基因的表达,从而导致发现新的转录本。除了表征正常和恶性基因表达模式,SAGE还可以用于鉴定肿瘤抑制因子和癌基因的下游靶标,并进一步注释基因组。使用SAGE对表达谱进行全面分析将产生许多新的诊断和预后标志物以及癌症的治疗靶标。

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