Comparison of protein expression profiles in NCI-60 cell panel containing nine difererent cancer tissue types.

Because most potential molecular markers and targets are proteins, proteomic profiling is expected to yield more direct answers to functional and pharmacological questions than does transcriptional profiling. To aid in such studies, we have developed a protocol for making reverse-phase protein lysate microarrays with larger numbers of spots than previously feasible. Our first application of these arrays was to profiling of the 60 human cancer cell lines (NCI-60) used by the National Cancer Institute to screen compounds for anticancer activity. Each glass slide microarray included 648 lysate spots representing the NCI-60 cell lines plus controls, each at 10 two-fold serial dilutions to provide a wide dynamic range. Mouse monoclonal antibodies and the catalyzed signal amplification system were used for immunoquantitation. The signal levels from the >30,000 data points for our first 52 antibodies were analyzed by using P-SCAN and a quantitative dose interpolation method. Clustered image maps revealed biologically interpretable patterns of protein expression. Among the principal early findings from these arrays were two promising pathological markers for distinguishing colon from ovarian adenocarcinomas. When we compared the patterns of protein expression with those we had obtained for the same genes at the mRNA level by using both cDNA and oligonucleotide arrays, a striking regularity appeared: cell-structure-related proteins almost invariably showed a high correlation between mRNA and protein levels across the NCI-60 cell lines, whereas non-cell-structure-related proteins showed poor correlation. http://discover.nci.nih.gov/host/2003_profiling_abstract.jsp Keywords: Cancer cell line comparison. Nine tissue types included in the NCI-60 panel are as follows: Breast, CNS, Colon, Lung, Melanoma, Leukemia, Ovary, Prostate and Renal. The NCI-60 cell line lysates were analyzed with using 176 antibodies that were prescreened to give highest quality by western blot analysis. Each array contained 64 samples (60 cancer cells and 4 control pool) in 10 serial dilutions.