Gene expression patterns of breast carcinomas distinguish tumor subclasses with clinical implications

被引:8212
作者
Sorlie, T
Perou, CM
Tibshirani, R
Aas, T
Geisler, S
Johnsen, H
Hastie, T
Eisen, MB
van de Rijn, M
Jeffrey, SS
Thorsen, T
Quist, H
Matese, JC
Brown, PO
Botstein, D
Lonning, PE
Borresen-Dale, AL [1 ]
机构
[1] Norwegian Radium Hosp, Dept Genet, N-0310 Oslo, Norway
[2] Norwegian Radium Hosp, Dept Surg, N-0310 Oslo, Norway
[3] Univ N Carolina, Dept Genet, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
[5] Stanford Univ, Sch Med, Howard Hughes Med Inst, Stanford, CA 94305 USA
[6] Stanford Univ, Sch Med, Dept Biochem, Stanford, CA 94305 USA
[7] Stanford Univ, Sch Med, Dept Surg, Stanford, CA 94305 USA
[8] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
[9] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
[10] Stanford Univ, Sch Med, Dept Hlth Res & Policy & Stat, Stanford, CA 94305 USA
[11] Haukeland Univ Hosp, Dept Med, Sect Oncol, N-5021 Bergen, Norway
[12] Haukeland Univ Hosp, Dept Surg, N-5021 Bergen, Norway
[13] Haukeland Univ Hosp, Dept Biochem Endocrinol, N-5021 Bergen, Norway
[14] Lawrence Orlando Berkeley Natl Labs, Div Life Sci, Berkeley, CA 94720 USA
[15] Univ Calif Berkeley, Dept Mol & Cellular Biol, Berkeley, CA 94720 USA
关键词
D O I
10.1073/pnas.191367098
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
The purpose of this study was to classify breast carcinomas based on variations in gene expression patterns derived from cDNA microarrays and to correlate tumor characteristics to clinical outcome. A total of 85 cDNA microarray experiments representing 78 cancers, three fibroadenomas, and four normal breast tissues were analyzed by hierarchical clustering. As reported previously, the cancers could be classified into a basal epithelial-like group, an ERBB2-overexpressing group and a normal breast-like group based on variations in gene expression. A novel finding was that the previously characterized luminal epithelial/estrogen receptor-positive group could be divided into at least two subgroups, each with a distinctive expression profile. These subtypes proved to be reasonably robust by clustering using two different gene sets: first, a set of 456 cDNA clones previously selected to reflect intrinsic properties of the tumors and, second, a gene set that highly correlated with patient outcome. Survival analyses on a subcohort of patients with locally advanced breast cancer uniformly treated in a prospective study showed significantly different outcomes for the patients belonging to the various groups, including a poor prognosis for the basal-like subtype and a significant difference in outcome for the two estrogen receptor-positive groups.
引用
收藏
页码:10869 / 10874
页数:6
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