Detecting Cancer Gene Networks Characterized by Recurrent Genomic Alterations in a Population

被引:20
作者
Efroni, Sol [1 ]
Ben-Hamo, Rotem [1 ]
Edmonson, Michael [3 ]
Greenblum, Sharon [3 ]
Schaefer, Carl F. [2 ]
Buetow, Kenneth H. [2 ,3 ]
机构
[1] Bar Ilan Univ, Mina & Everard Fac Life Sci, Ramat Gan, Israel
[2] NCI, Ctr Biomed Informat & Informat Technol, NIH, Bethesda, MD 20892 USA
[3] NIH, Lab Populat Genet, Bethesda, MD 20892 USA
来源
PLOS ONE | 2011年 / 6卷 / 01期
关键词
DNA COPY-NUMBER; UBIQUITIN-PROTEASOME PATHWAY; HIGH-RESOLUTION ANALYSIS; HUMAN BREAST-TUMORS; PATIENT SURVIVAL; P53; STATUS; HYBRIDIZATION; EXPRESSION; MICROARRAYS; REVEALS;
D O I
10.1371/journal.pone.0014437
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
High resolution, system-wide characterizations have demonstrated the capacity to identify genomic regions that undergo genomic aberrations. Such research efforts often aim at associating these regions with disease etiology and outcome. Identifying the corresponding biologic processes that are responsible for disease and its outcome remains challenging. Using novel analytic methods that utilize the structure of biologic networks, we are able to identify the specific networks that are highly significantly, nonrandomly altered by regions of copy number amplification observed in a systems-wide analysis. We demonstrate this method in breast cancer, where the state of a subset of the pathways identified through these regions is shown to be highly associated with disease survival and recurrence.
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页数:7
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