Asynchronous Replication in Lymphocytes from Patients with Inflammatory Bowel Disease and Primary Sclerosing Cholangitis

• Published in: Cytogenetic and genome research Vol. 145; no. 1; pp. 35 - 41
• Main Authors: Laish, Ido, Biron-Shental, Tal, Katz, Hila, Liberman, Meytal, Kitay-Cohen, Yona, Konikoff, Fred Meir, Amiel, Aliza
• Format: Journal Article
• Language: English
• Published: Basel, Switzerland S. Karger AG 01.01.2015
• Subjects: Cell Division - genetics; Cell Proliferation; Cells, Cultured; Cholangitis, Sclerosing - genetics; Colorectal Neoplasms - epidemiology; DNA Replication; Female; Humans; In Situ Hybridization, Fluorescence; Inflammatory Bowel Diseases - genetics; Lymphocytes - pathology; Male; Middle Aged; Original Article; Inflammatory bowel disease; Primary sclerosing cholangitis; Replication pattern; Asynchronous replication; Monoallelic expression
• ISSN: 1424-8581; 1424-859X; 1424-859X
• DOI: 10.1159/000381406

Primary sclerosing cholangitis (PSC) and inflammatory bowel disease (IBD) are associated chronic inflammatory diseases with malignant potential. Loss of replication synchrony during the S-phase of the cell cycle has been shown to be linked to several malignant and premalignant states. This study evaluated temporal differences in replication timing between these diseases. The replication pattern of peripheral blood lymphocytes obtained from patients with PSC and IBD and healthy individuals was analyzed by fluorescence in situ hybridization (FISH) in 2 pairs of alleles, in 15qter and 13qter. Asynchrony was determined by the presence of 1 single and 1 set of double dots in the same cell. Samples from subjects with PSC showed significantly greater temporal differences in replication timing, in contrast to the high level of synchrony observed in samples from healthy individuals (p = 0.045). Samples from IBD patients exhibited a nonsignificant increase in replication asynchrony. We believe that these results reflect impairment in the replication control of structural homologous loci in PSC, and that this phenomenon may be correlated with the inflammation-induced malignant potential of this condition.