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Analysis of gene network in MCF-7 human breast cancer cells

机译:MCF-7人乳腺癌细胞的基因网络分析

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Recent technological progress on high-throughput measurements for gene expression such as microarray analysis enables us to collect time-series gene expression data for each of tens of thousands of genes. Although a genomic analysis with those data has identified key genes relating to various diseases, few results on estimation of gene regulatory networks with real microarray data are available so far. Recently, the immediately early response (1ER) genes upon epidermal growth factor stimulation in a human breast cancer cell line, MCF-7, have been identified in which time-course microarray data were measured during 90 minutes and 63 1ER genes were chosen from tens of thousands of genes by using statistical analysis. In this paper, we estimate the gene regulatory networks among the 63 1ER genes. To this end, we apply an estimation method based on a mixed logic dynamical modeling developed in an earlier study to the microarray data. However, the original method is executable for continuous gene expression time-series data whereas the real microarray time-course data have very few time points. In addition, some presetting parameters in the model are critical for a successful result on a network estimation. Then, we add a preprocessing and Monte Carlo-based calculation for die original method.
机译:基因表达的高通量测量(例如微阵列分析)方面的最新技术进步使我们能够收集成千上万个基因的时序基因表达数据。尽管利用这些数据进行的基因组分析已经确定了与各种疾病有关的关键基因,但到目前为止,利用真实的微阵列数据估算基因调控网络的结果很少。最近,已经确定了在人乳腺癌细胞MCF-7中表皮生长因子刺激后的立即早期反应(1ER)基因,其中在90分钟内测量了时程微阵列数据,并从数十种中选择了63种1ER基因。通过统计分析分析成千上万的基因在本文中,我们估计了63个1ER基因之间的基因调控网络。为此,我们将基于早期研究中开发的混合逻辑动态建模的估计方法应用于微阵列数据。但是,原始方法可用于连续基因表达时间序列数据,而真正的微阵列时程数据只有很少的时间点。此外,模型中的一些预设参数对于网络估计的成功结果至关重要。然后,我们为原始方法添加了预处理和基于Monte Carlo的计算。

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