通过网络正则化Cox模型识别癌症生物标志物

Ying-Wooi Wan, John Nagorski, Genevera I. Allen, Zhaohui Li, Zhandong Liu
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引用次数: 7

摘要

癌症基因组学的一个核心问题是确定可解释的生物标志物,以获得更好的疾病预后。通过Cox比例风险(PH)模型确定的许多生物标志物在生物学上是不可解释的。我们提出使用图拉普拉斯正则化Cox PH模型将生物网络整合到生存分析中的特征选择问题中。仿真研究表明,该算法的性能优于L1和L1+L2正则化Cox PH模型。利用cancer Genome Altas联盟生成的基因组畸变数据,该算法能够识别雌激素受体阳性乳腺癌患者的关键已知生物标志物,如p53和myc,从而验证了该算法的实用性。随着我们对生物网络知识的快速扩展,这种方法对于挖掘高通量基因组数据集将变得越来越有用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identifying cancer biomarkers through a network regularized Cox model
A central problem in cancer genomics is to identify interpretable biomarkers for better disease prognosis. Many of the biomarkers identified through Cox Proportional Hazard (PH) models are biologically uninterpretable. We propose the use of graph Laplacian regularized Cox PH model to integrate biological networks into the feature selection problem in survival analysis. Simulation studies demonstrate that the performance of the proposed algorithm is superior to L1 and L1+L2 regularized Cox PH models. Utility of this algorithm is also validated by its ability to identify key known biomarkers such as p53 and myc in estrogen receptor positive breast cancer patients using genomic abberration data generated by the Cancer Genome Altas consortium. With the rapid expansion of our knowledge of biological networks, this approach will become increasingly useful for mining high-throughput genomic datasets.
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