Distinctive gene expression patterns in human mammary epithelial cells and breast cancers

被引:1072
作者
Perou, CM
Jeffrey, SS
Van de Rijn, M
Rees, CA
Eisen, MB
Ross, DT
Pergamenschikov, A
Williams, CF
Zhu, SX
Lee, JCF
Lashkari, D
Shalon, D
Brown, PO [1 ]
Botstein, D
机构
[1] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Surg, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Dept Biochem, Stanford, CA 94305 USA
[5] Stanford Univ, Sch Med, Howard Hughes Med Inst, Stanford, CA 94305 USA
[6] Incyte Pharmaceut Inc, Fremont, CA 94555 USA
[7] Geometrix, The Woodlands, TX 77381 USA
关键词
D O I
10.1073/pnas.96.16.9212
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
cDNA microarrays and a clustering algorithm were used to identify patterns of gene expression in human mammary epithelial cells growing in culture and in primary human breast tumors. Clusters of coexpressed genes identified through manipulations of mammary epithelial cells in vitro also showed consistent patterns of variation in expression among breast tumor samples. By using immunohistochemistry with antibodies against proteins encoded by a particular gene in a cluster, the identity of the cell type within the tumor specimen that contributed the observed gene expression pattern could be determined. Clusters of genes with coherent expression patterns in cultured cells and in the breast tumors samples could he related to specific features of biological variation among the samples. Two such clusters were found to have patterns that correlated with variation in cell proliferation rates and with activation of the IFN-regulated signal transduction pathway, respectively. Clusters of genes expressed by stromal cells and lymphocytes in the breast tumors also were identified in this analysis. These results support the feasibility and usefulness of this systematic approach to studying variation in gene expression patterns in human cancers as a means to dissect and classify solid tumors.
引用
收藏
页码:9212 / 9217
页数:6
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