1. Combined α-methylacyl coenzyme A racemase/p53 analysis to identify dysplasia in inflammatory bowel disease
- Author
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Achim Fleischmann, Timo Wandrey, Nib Soehendra, Tobias Grob, Jussuf T. Kaifi, Sarah Minner, Guido Sauter, Uwe Seitz, Philipp W. Simon, Stefan Seewald, Martina Mirlacher, Ronald Simon, Luigi Terracciano, Andreas Raedler, Uta Reichelt, Wolfgang Tigges, Martina E. Spehlmann, Agatha Wewer, Andreas H. Marx, Emre F. Yekebas, and Jakob R. Izbicki
- Subjects
medicine.medical_specialty ,Pathology ,Coenzyme A ,Racemases and Epimerases ,Biology ,Polymerase Chain Reaction ,Sensitivity and Specificity ,Inflammatory bowel disease ,Gastroenterology ,Pathology and Forensic Medicine ,chemistry.chemical_compound ,Internal medicine ,Biomarkers, Tumor ,medicine ,Carcinoma ,Humans ,Neoplastic transformation ,Cyclin-Dependent Kinase Inhibitor p16 ,Tissue microarray ,Anatomical pathology ,Inflammatory Bowel Diseases ,medicine.disease ,Immunohistochemistry ,Ulcerative colitis ,Proto-Oncogene Proteins c-bcl-2 ,chemistry ,Tissue Array Analysis ,Dysplasia ,Disease Progression ,Tumor Suppressor Protein p53 ,Precancerous Conditions - Abstract
Identification of dysplasia in inflammatory bowel disease represents a major challenge for both clinicians and pathologists. Clear diagnosis of dysplasia in inflammatory bowel disease is sometimes not possible with biopsies remaining "indefinite for dysplasia." Recent studies have identified molecular alterations in colitis-associated cancers, including increased protein levels of alpha-methylacyl coenzyme A racemase, p53, p16 and bcl-2. In order to analyze the potential diagnostic use of these parameters in biopsies from inflammatory bowel disease, a tissue microarray was manufactured from colons of 54 patients with inflammatory bowel disease composed of 622 samples with normal mucosa, 78 samples with inflammatory activity, 6 samples with low-grade dysplasia, 12 samples with high-grade dysplasia, and 66 samples with carcinoma. In addition, 69 colonoscopic biopsies from 36 patients with inflammatory bowel disease (28 low-grade dysplasia, 8 high-grade dysplasia, and 33 indefinite for dysplasia) were included in this study. Immunohistochemistry for alpha-methylacyl coenzyme A racemase, p53, p16 and bcl-2 was performed on both tissue microarray and biopsies. p53 and alpha-methylacyl coenzyme A racemase showed the most discriminating results, being positive in most cancers (77.3% and 80.3%) and dysplasias (94.4% and 94.4%) but only rarely in nonneoplastic epithelium (1.6% and 9.4%; P < .001). Through combining the best discriminators, p53 and alpha-methylacyl coenzyme A racemase, a stronger distinction between neoplastic tissues was possible. Of all neoplastic lesions, 75.8% showed a coexpression of alpha-methylacyl coenzyme A racemase and p53, whereas this was found in only 4 of 700 nonneoplastic samples (0.6%). alpha-methylacyl coenzyme A racemase/p53 coexpression was also found in 10 of 33 indefinite for dysplasia biopsies (30.3 %), suggesting a possible neoplastic transformation in these cases. Progression to dysplasia or carcinoma was observed in 3 of 10 p53/alpha-methylacyl coenzyme A racemase-positive, indefinite-for-dysplasia cases, including 1 of 7 cases without and 2 of 3 cases with p53 mutation. It is concluded that combined alpha-methylacyl coenzyme A racemase/p53 analysis may represent a helpful tool to confirm dysplasia in inflammatory bowel disease.
- Published
- 2009