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Use of gene expression to identify heterogeneity of metastatic behavior among high-grade pleomorphic soft tissue sarcomas Keith Skubitz1, Princy Francis2, Amy Skubitz1, Xianghua Luo1, and Mef Nilbert2,3 1University of Minnesota, 2Lund University, 3Hvidovre Hospital Sarcomas are heterogeneous Heterogeneity of biological behavior exists even within histologic subtypes of sarcomas, complicating clinical care, clinical trials, and drug development. Example Assume treatment A has no adverse effect Assume benefit of treatment A is all or none in a certain percentage of patients Some biological behaviors that do not correlate well with morphology may be determined by gene expression patterns A common approach to identify prognostic factors is to search for differences in gene expression between 2 groups defined by an outcome (eg survival) Requires defining 2 groups Irrelevant genes may obscure important patterns Different genes could be important in different subsets Alternatively, identification of subsets independent of clinical information could be useful We used PCA with a variety of gene sets in an attempt to identify heterogeneity Clear cell renal carcinoma (RCC) Serrous ovarian carcinoma (OVCA) Aggressive fibromatosis (AF) PCA with 604 probes up or down /=5-fold in ccRCC vs normal kidney PCA with probes from ubiquitylation in control of cell cycle pathway Gene expression patterns that distinguished 2 subsets of RCC (RCC gene set), OVCA (OVCA gene set), and AF (AF gene set) were identified Question Do the RCC-, OVCA-, and AF-gene sets identify subsets of high-grade pleomorphic STS? Samples 73 Samples obtained from Lund University 40 MFH 20 LMS 9 other high-grade pleomorphic STS Data cDNA microarray slides with ~16,000 unique UniGene clusters About 50% of the genes in the RCC-, OVCA-, and AF- gene sets were present in this data set Methods Data were pooled to form a set of 234 genes present in at least one of the RCC-, OVCA-, or AF-gene sets Hierarchical
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