A signature of chromosomal instability inferred from gene expression profiles predicts clinical outcome in multiple human cancers

被引:922
作者
Carter, Scott L.
Eklund, Aron C.
Kohane, Isaac S.
Harris, Lyndsay N.
Szallasi, Zoltan [1 ]
机构
[1] Harvard Univ, Childrens Hosp, Sch Med, Harvard Mit Div Hlth Sci & Technol,Informat Progr, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Lab Funct Geonom, Cambridge, MA 02139 USA
[3] Yale Univ, Sch Med, Breast Dis Unit, New Haven, CT 06520 USA
[4] Tech Univ Denmark, Ctr Biol Sequence Anal, DK-2800 Lyngby, Denmark
关键词
D O I
10.1038/ng1861
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We developed a computational method to characterize aneuploidy in tumor samples based on coordinated aberrations in expression of genes localized to each chromosomal region. We summarized the total level of chromosomal aberration in a given tumor in a univariate measure termed total functional aneuploidy. We identified a signature of chromosomal instability from specific genes whose expression was consistently correlated with total functional aneuploidy in several cancer types. Net overexpression of this signature was predictive of poor clinical outcome in 12 cancer data sets(1-12) representing six cancer types. Also, the signature of chromosomal instability was higher in metastasis samples than in primary tumors and was able to stratify grade 1 and grade 2 breast tumors according to clinical outcome. These results provide a means to assess the potential role of chromosomal instability in determining malignant potential over a broad range of tumors.
引用
收藏
页码:1043 / 1048
页数:6
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