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[Cancer Research 64, 1584-1588, March 1, 2004]
© 2004 American Association for Cancer Research


Advances in Brief

An Unsupervised Approach to Identify Molecular Phenotypic Components Influencing Breast Cancer Features

Florin M. Selaru1, Jing Yin1, Andreea Olaru1, Yuriko Mori1, Yan Xu1, Steven H. Epstein1, Fumiaki Sato2, Elena Deacu1, Suna Wang1, Anca Sterian1, Amy Fulton2, John M. Abraham1, David Shibata3, Claudia Baquet4, Sanford A. Stass2 and Stephen J. Meltzer1,2

1 Department of Medicine, Division of Gastroenterology, and 2 Departments of Pathology, 3 Surgery, 4 Epidemiology and Preventive Medicine, and University of Maryland Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, Maryland

To discover a biological basis for clinical subgroupings within breast cancers, we applied principal components (PCs) analysis to cDNA microarray data from 36 breast cancers. We correlated the resulting PCs with clinical features. The 35 PCs discovered were ranked in order of their impact on gene expression patterns. Interestingly, PC 7 identified a unique subgroup consisting of estrogen receptor (ER); (+) African-American patients. This group exhibited global molecular phenotypes significantly different from both ER (-) African-American women and ER (+) or ER (-) Caucasian women (P < 0.001). Additional significant PCs included PC 4, correlating with lymph node metastasis (P = 0.04), and PC 10, with tumor stage (stage 2 versus stage 3; P = 0.007). These results provide a molecular phenotypic basis for the existence of a biologically unique subgroup comprising ER (+) breast cancers from African-American patients. Moreover, these findings illustrate the potential of PCs analysis to detect molecular phenotypic bases for relevant clinical or biological features of human tumors in general.




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Copyright © 2004 by the American Association for Cancer Research.