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Prioritizing breast cancer subtype related miRNAs using miRNA-mRNA dysregulated relationships extracted from their dual expression profiling

机译:使用从其双重表达谱中提取的miRNA-mRNA失调关系来优先处理与乳腺癌亚型相关的miRNA

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Identification of miRNA expression-based breast cancer subtypes is considered a critical means of prognostication. So far, the studies on breast cancer subtypes have not been well characterized, and few studies have performed expression profiling of both miRNA and mRNA from the same breast cancer subtypes samples. In this study we analyzed dual expression profiling data of miRNA and mRNA derived from the expression profiling of 489 miRNAs in 41 luminal-A breast tumors samples and 15 basal-like samples. We defined a correlation coefficient ratio (CCR) and used it to examine the correlative dysregulated relationships between miRNAs and mRNAs. A miRNA-mRNA dysregulated network was arisen from 6222 dysregulated relationships, and from this network, miRNA-miRNA networks specialized for luminal-A and basal-like breast cancer subtypes were extracted according to the CCR values. By analyzing the networks, we found that luminal-A trend and basal-like trend miRNA-miRNA network displayed a change in hubs which connected the most miRNAs, and therefore become the potential breast cancer subtype related miRNAs. In addition, we also used other network analysis methods for miRNA expression profiling data, such as weighted correlation network analysis (WGCNA), Bayesian network analysis, and miRNA similarity (MISIM) analysis to validate the identified miRNAs or miRNA clusters. This study provides a new analyzing method to predict candidate miRNAs of breast cancer subtype from a system biology level and help understanding the relationship between miRNA and mRNA in primary breast cancer subtype.
机译:基于miRNA表达的乳腺癌亚型的鉴定被认为是预后的关键手段。到目前为止,关于乳腺癌亚型的研究尚未得到很好的表征,很少有研究对同一乳腺癌亚型样品中的miRNA和mRNA进行表达谱分析。在这项研究中,我们分析了miRNA和mRNA的双重表达谱数据,这些数据来自41个腔A乳腺肿瘤样品和15个基底样样品中489个miRNA的表达谱。我们定义了一个相关系数比(CCR),并用它来检查miRNA和mRNA之间的相关失调关系。 miRNA-mRNA失调网络是由6222个失调关系产生的,并且根据该CCC值,提取了专门用于腔A和基底样乳腺癌亚型的miRNA-miRNA网络。通过分析网络,我们发现腔A趋势和基底样趋势miRNA-miRNA网络在连接大多数miRNA的集线器中显示出变化,因此成为潜在的与乳腺癌亚型相关的miRNA。此外,我们还使用其他网络分析方法来处理miRNA表达谱数据,例如加权相关网络分析(WGCNA),贝叶斯网络分析和miRNA相似性(MISIM)分析,以验证已识别的miRNA或miRNA簇。这项研究提供了一种新的分析方法,可以从系统生物学水平预测乳腺癌亚型的候选miRNA,并有助于了解原发性乳腺癌亚型中miRNA与mRNA的关系。

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