Pang Herbert, Zhao Hongyu
Department of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC, USA. ; School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
Department of Biostatistics, Yale School of Public Health, New Haven, CT, USA.
Cancer Inform. 2014 Dec 9;13(Suppl 4):73-8. doi: 10.4137/CIN.S13973. eCollection 2014.
Cancer biomarker discovery can facilitate drug development, improve staging of patients, and predict patient prognosis. Because cancer is the result of many interacting genes, analysis based on a set of genes with related biological functions or pathways may be more informative than single gene-based analysis for cancer biomarker discovery. The relevant pathways thus identified may help characterize different aspects of molecular phenotypes related to the tumor. Although it is well known that cancer patients may respond to the same treatment differently because of clinical variables and variation of molecular phenotypes, this patient heterogeneity has not been explicitly considered in pathway analysis in the literature. We hypothesize that combining pathway and patient clinical information can more effectively identify relevant pathways pertinent to specific patient subgroups, leading to better diagnosis and treatment. In this article, we propose to perform stratified pathway analysis based on clinical information from patients. In contrast to analysis using all the patients, this more focused analysis has the potential to reveal subgroup-specific pathways that may lead to more biological insights into disease etiology and treatment response. As an illustration, the power of our approach is demonstrated through its application to a breast cancer dataset in which the patients are stratified according to their oral contraceptive use.
癌症生物标志物的发现有助于药物研发、改善患者分期并预测患者预后。由于癌症是众多相互作用基因的结果,基于一组具有相关生物学功能或通路的基因进行分析,对于癌症生物标志物的发现可能比基于单个基因的分析更具信息量。由此确定的相关通路可能有助于刻画与肿瘤相关的分子表型的不同方面。尽管众所周知,由于临床变量和分子表型的差异,癌症患者对相同治疗的反应可能不同,但文献中的通路分析尚未明确考虑这种患者异质性。我们假设,将通路信息与患者临床信息相结合能够更有效地识别与特定患者亚组相关的通路,从而实现更好的诊断和治疗。在本文中,我们建议基于患者的临床信息进行分层通路分析。与对所有患者进行分析相比,这种更具针对性的分析有可能揭示亚组特异性通路,从而对疾病病因和治疗反应获得更多生物学见解。作为例证,我们通过将该方法应用于一个乳腺癌数据集来展示其效力,在该数据集中,患者根据口服避孕药的使用情况进行了分层。