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首页> 外文期刊>BMC Bioinformatics >Regularized logistic regression with network-based pairwise interaction for biomarker identification in breast cancer
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Regularized logistic regression with network-based pairwise interaction for biomarker identification in breast cancer

机译:基于网络的成对交互的正则逻辑回归用于乳腺癌生物标志物识别

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Backgroud To facilitate advances in personalized medicine, it is important to detect predictive, stable and interpretable biomarkers related with different clinical characteristics. These clinical characteristics may be heterogeneous with respect to underlying interactions between genes. Usually, traditional methods just focus on detection of differentially expressed genes without taking the interactions between genes into account. Moreover, due to the typical low reproducibility of the selected biomarkers, it is difficult to give a clear biological interpretation for a specific disease. Therefore, it is necessary to design a robust biomarker identification method that can predict disease-associated interactions with high reproducibility. Results In this article, we propose a regularized logistic regression model. Different from previous methods which focus on individual genes or modules, our model takes gene pairs, which are connected in a protein-protein interaction network, into account. A line graph is constructed to represent the adjacencies between pairwise interactions. Based on this line graph, we incorporate the degree information in the model via an adaptive elastic net, which makes our model less dependent on the expression data. Experimental results on six publicly available breast cancer datasets show that our method can not only achieve competitive performance in classification, but also retain great stability in variable selection. Therefore, our model is able to identify the diagnostic and prognostic biomarkers in a more robust way. Moreover, most of the biomarkers discovered by our model have been verified in biochemical or biomedical researches. Conclusions The proposed method shows promise in the diagnosis of disease pathogenesis with different clinical characteristics. These advances lead to more accurate and stable biomarker discovery, which can monitor the functional changes that are perturbed by diseases. Based on these predictions, researchers may be able to provide suggestions for new therapeutic approaches.
机译:背景技术为了促进个性化医学的发展,检测与不同临床特征相关的可预测,稳定和可解释的生物标记很重要。就基因之间的潜在相互作用而言,这些临床特征可能是异质的。通常,传统方法只专注于差异表达基因的检测,而没有考虑基因之间的相互作用。而且,由于所选生物标志物的典型的低再现性,难以对特定疾病给出清晰的生物学解释。因此,有必要设计一种鲁棒的生物标志物鉴定方法,该方法可以高再现性地预测疾病相关的相互作用。结果在本文中,我们提出了一个正规化的逻辑回归模型。与以前关注单个基因或模块的方法不同,我们的模型考虑了通过蛋白质-蛋白质相互作用网络连接的基因对。构造线图以表示成对交互之间的邻接。基于此线图,我们通过自适应弹性网将度信息合并到模型中,这使我们的模型较少依赖于表达式数据。在六个可公开获得的乳腺癌数据集上的实验结果表明,我们的方法不仅可以实现分类方面的竞争性能,而且在变量选择上也保持了很大的稳定性。因此,我们的模型能够以更可靠的方式识别诊断和预后生物标志物。此外,我们的模型发现的大多数生物标志物已在生化或生物医学研究中得到验证。结论所提出的方法在诊断具有不同临床特征的疾病发病机理方面具有广阔的前景。这些进展导致更准确,更稳定的生物标志物发现,可以监测受到疾病干扰的功能变化。基于这些预测,研究人员可能能够为新的治疗方法提供建议。

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