HISTOLOGY AND HISTOPATHOLOGY

Cellular and Molecular Biology



Review

Expression of differentiation-related genes in colorectal cancer: possible implications for prognosis

N. van Belzen1, W.N.M. Dinjens2, B.H.J. Eussen3 and F.T. Bosman4

1Institute of Hematology, 2Department of Pathology, and 3Department of Clinical Genetics, Erasmus University Rotterdam, Rotterdam, The Netherlands and 4Department of Pathology, University of Lausanne, Lausanne, Switzerland

Offprint requests to: Dr. N. van Belzen, PhD, Nutrition Expertise Centre DMV International / Campina Melkunie, p/a DMV International R&A, P.O. Box 13, 5460 BA Veghel, The Netherlands. Fax: 31-413-365536. e-mail: belzen@hotmail.com

 

Summary. Although differentiation grade is an important prognostic factor for colorectal tumors, its usefulness is limited since its predictive value for tumor behavior is not very significant. This might be related to the subjective nature of histological assessment of differentiation grade, which allows the distinction of only three grades, and with limited reproducibility. Characterization of the differentiation process at the biochemical level may improve our understanding of normal and malignant differentiation, and is expected to provide molecular markers with higher discriminative potential than histomorphology. Several studies have compared gene expression in undifferentiated and differentiated colon carcinoma cells, and many differentially expressed genes have been identified. Some of these, including HLA class I, nucleophosmin, adenylosuccinate lyase, a-tubulin, and a novel gene designated Drg1, were found to be expressed at different levels in neoplastic as compared to normal tissue. In this review the rationale, implementation, and results of this approach are discussed, as well as the characteristics of two novel differentially expressed genes, ICT1 (previously named DS-1) and Drg1. Histol. Histopathol. 13, 1233-1242 (1998)

 

Key words: Colon epithelium, Colorectal carcinoma, Differentiation, Marker, Myeloid, ICT1, Drg1

DOI: 10.14670/HH-13.1233