REG1A expression is a prognostic marker in colorectal cancer and associated with peritoneal carcinomatosis

• Published in: International journal of cancer 2008-07, Vol.123 (2), p.409-413
• Main Authors: Astrosini, Christian, Roeefzaad, Claudia, Dai, Yi‐Yang, Dieckgraefe, Brian K., Jöns, Thomas, Kemmner, Wolfgang
• Format: Article
• Language: English
• Subjects: Biological and medical sciences; Biomarkers, Tumor - metabolism; Carcinoma - metabolism; Carcinoma - secondary; colorectal cancer; Colorectal Neoplasms - metabolism; Colorectal Neoplasms - pathology; Gastroenterology. Liver. Pancreas. Abdomen; Gene Expression Profiling; Gene Expression Regulation, Neoplastic; Humans; Immunohistochemistry; Intestinal Mucosa - metabolism; Kaplan-Meier Estimate; Lithostathine - metabolism; Medical sciences; Neoplasm Staging; Oligonucleotide Array Sequence Analysis; peritoneal carcinomatosis; Peritoneal Neoplasms - metabolism; Peritoneal Neoplasms - secondary; Polymerase Chain Reaction; Predictive Value of Tests; Prognosis; prognostic factors; REG1A; Reproducibility of Results; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus; Tumors; Up-Regulation
• ISSN: 0020-7136; 1097-0215
• DOI: 10.1002/ijc.23466

By expression profiling of early staged colon carcinomas, we found regenerating islet‐derived 1 alpha (REG1A) to be upregulated in patients with an unfavorable clinical outcome. For validation, REG1A expression was quantified in another colorectal cancer (CRC) patient cohort by Taqman PCR. Aside from tumor and normal tissue from 63 nonpretreated CRC patients, 31 mucosa biopsies from healthy individuals as well as 22 adenomas were included in the investigation. REG1A was significantly upregulated in tumor specimens (p < 0.001) and adenoma (p < 0.01) as compared to normal colorectal tissue. REG1A expression in normal peritumoral tissue in turn proved to be significantly elevated compared to mucosa from healthy individuals (p < 0.01). Determination of REG1A expression might be useful for early tumor diagnosis with a sensitivity of 90.6%, and a specificity of 77.9%. REG1A expression was significantly increased in tumors with peritoneal carcinomatosis (p < 0.01). Moreover, REG1A turned out to be a significant predictor of disease‐free survival (p < 0.05). In conclusion, we present evidence that REG1A is a molecular marker of prognostic value and is associated with peritoneal carcinomatosis in CRC. REG1A turned out to be already significantly raised in peritumoral normal tissue compared to mucosa from healthy individuals, suggesting a molecular field effect of secreted REG1A. © 2008 Wiley‐Liss, Inc.