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Methylation, Copy Number, and LOH Analysis of Chr8q24 for Discovery of Ovarian and Breast Cancer Biomarkers

机译:CHR8Q24发现卵巢癌生物标志物的甲基化,拷贝数和LOH分析

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The association of genetic abnormalities and specific cancers is leading to an increasing number of biomarkers that can be used for early detection of cancers, determination of treatment protocols and predicted prognoses. Additionally, the methylation state of an increasing number of genes is also producing possible predictive biomarkers for specific cancers and stages of cancer as well. To this end, we have analyzed both breast and ovarian cancers and their normal adjacent tissue using both DNA methylation analysis and genome wide array screening for LOH and copy number variations. The combination of these two methods has yielded several groupings of markers that are cancer specific as well as showing specificity for the specific tumor type. Specifically, there are increased copies in the chr8q24 region in both ovarian and breast tumor DNA and differences in the methylation between the two tumor DNAs. We will present the results of the combination of the genome wide analysis and DNA methylation results that may be used in combination to produce potential biomarkers for these two cancer types.
机译:遗传异常和特异性癌症的关联导致越来越多的生物标志物,可用于早期检测癌症,治疗方案的测定和预测预测。另外,越来越多的基因的甲基化状态也为特异性癌症和癌症的阶段产生了可能的预测生物标志物。为此,我们使用DNA甲基化分析和基因组宽阵列筛选来分析乳腺癌和卵巢癌和它们的正常相邻组织,用于LOH和拷贝数变化。这两种方法的组合产生了几种是癌症的标记物,以及表现出特定肿瘤类型的特异性。具体地,在卵巢肿瘤和乳腺肿瘤DNA中的CHR8Q24区域中存在增加的拷贝,并且两种肿瘤DNA之间的甲基化的差异。我们将提出基因组广泛分析和DNA甲基化结果的组合结果,其可以组合使用以产生这两种癌症类型的潜在生物标志物。

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