Detection of gene pathways with predictive power for breast cancer prognosis

被引:20
|
作者
Ma, Shuangge [1 ]
Kosorok, Michael R. [2 ]
机构
[1] Yale Univ, Sch Publ Hlth, New Haven, CT 06520 USA
[2] Univ N Carolina, Dept Biostat, Chapel Hill, NC 27599 USA
来源
BMC BIOINFORMATICS | 2010年 / 11卷
基金
美国国家科学基金会;
关键词
MICROARRAY DATA; ASYMPTOTIC PROPERTIES; HISTOLOGIC GRADE; EXPRESSION; CLASSIFICATION; IDENTIFICATION; SELECTION; AUTOTAXIN; RECEPTOR;
D O I
10.1186/1471-2105-11-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Prognosis is of critical interest in breast cancer research. Biomedical studies suggest that genomic measurements may have independent predictive power for prognosis. Gene profiling studies have been conducted to search for predictive genomic measurements. Genes have the inherent pathway structure, where pathways are composed of multiple genes with coordinated functions. The goal of this study is to identify gene pathways with predictive power for breast cancer prognosis. Since our goal is fundamentally different from that of existing studies, a new pathway analysis method is proposed. Results: The new method advances beyond existing alternatives along the following aspects. First, it can assess the predictive power of gene pathways, whereas existing methods tend to focus on model fitting accuracy only. Second, it can account for the joint effects of multiple genes in a pathway, whereas existing methods tend to focus on the marginal effects of genes. Third, it can accommodate multiple heterogeneous datasets, whereas existing methods analyze a single dataset only. We analyze four breast cancer prognosis studies and identify 97 pathways with significant predictive power for prognosis. Important pathways missed by alternative methods are identified. Conclusions: The proposed method provides a useful alternative to existing pathway analysis methods. Identified pathways can provide further insights into breast cancer prognosis.
引用
收藏
页数:11
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