Proteomic analysis of colonic crypts from normal, multiple intestinal neoplasia and p53-null mice: A comparison with colonic polyps
Author(s)
Cole, AR; Ji, H; Simpson, RJ;
Details
Publication Year 2000-05,Volume 21,Issue #9,Page 1772-1781
Journal Title
ELECTROPHORESIS
Publication Type
Journal Article
Abstract
In order to observe cellular changes caused by mutation of the tumor suppressors, APC and p53, we have generated protein expression profiles of mouse colon epithelial cells using two-dimensional electrophoresis (2-DE). Crypts, polyps and stroma were isolated from normal, multiple intestinal neoplasia (MIN) ana p53-null mice, each with a C57Black/6J background, and subjected to 2-DE in two separate pH ranges (pH 3-10 and pH 6-11). No significant differences in protein expression patterns were observed between the normal, MIN and p53-null colon epithelial crypts. However, 64 proteins from the MIN polyps showed a 2-fold or greater difference in intensity that was statistically significant as assessed by the Wilcoxon rank-sum test (p less than or equal to 0.05). Of these, calreticulin, carbonic anhydrase I and a new member of the glutathione-S-transferase theta family of proteins have so far been identified using an in-gel digestion protocol coupled with reversed-phase high performance liquid chromatography (RP-HPLC) ion-trap mass spectrometry. In addition, 38 marker proteins have been identified in a continuing effort to generate a comprehensive 2-DE database of proteins expressed by mouse colon epithelial cells (these databases are available at http:/www. ludwig.edu.au/jpsl/jpSlhome.html.).
Publisher
WILEY-V C H VERLAG GMBH
Keywords
HUMAN COLORECTAL-CANCER; TUMOR-SUPPRESSOR GENE; CELL-CYCLE CONTROL; WILD-TYPE P53; BETA-CATENIN; CYCLOOXYGENASE-2 LEVELS; SEPARATED PROTEINS; CARBONIC-ANHYDRASE; MESSENGER-RNA; UP-REGULATION
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Creation Date: 2000-05-01 12:00:00
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