1. Molecular alterations in pancreatic carcinoma: expression profiling shows that dysregulated expression of S100 genes is highly prevalent.
- Author
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Crnogorac-Jurcevic T, Missiaglia E, Blaveri E, Gangeswaran R, Jones M, Terris B, Costello E, Neoptolemos JP, and Lemoine NR
- Subjects
- Adenocarcinoma metabolism, Calcium-Binding Proteins genetics, DNA, Neoplasm genetics, Gene Expression Profiling, Humans, Oligonucleotide Array Sequence Analysis, Pancreatic Neoplasms metabolism, S100 Calcium Binding Protein A6, S100 Proteins metabolism, Tumor Cells, Cultured, Adenocarcinoma genetics, Biomarkers, Tumor metabolism, Cell Cycle Proteins, Gene Expression Regulation, Neoplastic, Neoplasm Proteins, Pancreatic Neoplasms genetics, S100 Proteins genetics
- Abstract
In order to expand our understanding of the molecular changes underlying the complex pathology of pancreatic malignancy, global gene expression profiling of pancreatic adenocarcinoma compared with normal pancreatic tissue was performed. Human cDNA arrays comprising 9932 elements were interrogated with fluorescence-labelled normal and adenocarcinoma samples (nine tumours, three normal pancreata, and three cell lines). The data were analysed for differential gene expression, which was confirmed by serial analysis of gene expression (SAGE), digital differential display (DDD) analysis, and immunohistochemistry for selected cases. The array data were filtered to produce lists of a total of 75 genes significantly up-regulated or down-regulated in pancreatic adenocarcinoma. Two of those showing the highest differential were members of the S100 family of Ca-binding proteins, namely S100P and S100A6, and therefore the S100 genes were studied in more detail. By immunohistochemical analysis of custom-built, pancreas-specific tissue arrays and commercially available, normal/cancer tissue arrays that included a wide variety of different tumour types, differential expression of S100P protein was found to be almost exclusive to pancreatic cancer. S100P could therefore represent a useful biomarker for pancreatic adenocarcinomas., (Copyright 2003 John Wiley & Sons, Ltd.)
- Published
- 2003
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