Systematic variation in gene expression patterns in human cancer cell lines

被引:1633
作者
Ross, DT
Scherf, U
Eisen, MB
Perou, CM
Rees, C
Spellman, P
Iyer, V
Jeffrey, SS
Van de Rijn, M
Waltham, M
Pergamenschikov, A
Lee, JCE
Lashkari, D
Shalon, D
Myers, TG
Weinstein, JN
Botstein, D
Brown, PO [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Biochem, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Surg, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
[5] NCI, Mol Pharmacol Lab, Div Basic Sci, NIH, Bethesda, MD 20892 USA
[6] Incyte Pharmaceut, Fremont, CA USA
[7] Genometrix Inc, The Woodlands, TX USA
[8] NCI, Informat Technol Branch, Dev Therapeut Program, Div Canc Treatment & Diagnosis,NIH, Rockville, MD USA
[9] Stanford Univ, Sch Med, Howard Hughes Med Inst, Stanford, CA 94305 USA
关键词
D O I
10.1038/73432
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We used cDNA microarrays to explore the variation in expression of approximately 8,000 unique genes among the 60 cell lines used in the National Cancer Institute's screen for anti-cancer drugs. Classification of the cell lines based solely on the observed patterns of gene expression revealed a correspondence to the ostensible origins of the tumours from which the cell lines were derived. The consistent relationship between the gene expression patterns and the tissue of origin allowed us to recognize outliers whose previous classification appeared incorrect. Specific features of the gene expression patterns appeared to be related to physiological properties of the cell lines, such as their doubling time in culture, drug metabolism or the interferon response. Comparison of gene expression patterns in the cell lines to those observed in normal breast tissue or in breast tumour specimens revealed features of the expression patterns in the tumours that had recognizable counterparts in specific cell lines, reflecting the tumour, stromal and inflammatory components of the tumour tissue. These results provided a novel molecular characterization of this important group of human cell lines and their relationships to tumours in vivo.
引用
收藏
页码:227 / 235
页数:9
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