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World J Gastroenterol. Apr 7, 2006; 12(13): 2109-2114
Published online Apr 7, 2006. doi: 10.3748/wjg.v12.i13.2109
Circadian variation in expression of G1 phase cyclins D1 and E and cyclin-dependent kinase inhibitors p16 and p21 in human bowel mucosa
John Griniatsos, Othon P Michail, Stamatios Theocharis, Antonios Arvelakis, Ioannis Papaconstantinou, Evangelos Felekouras, Emmanouel Pikoulis, Ioannis Karavokyros, Chris Bakoyiannis, George Marinos, John Bramis, Panayiotis O Michail
John Griniatsos, Othon P Michail, Antonios Arvelakis, Ioannis Papaconstantinou, Evangelos Felekouras, Emmanouel Pikoulis, Ioannis Karavokyros, Chris Bakoyiannis, George Marinos, John Bramis, Panayiotis O Michail, 1st Department of Surgery, Medical School, University of Athens, Greece
Stamatios Theocharis, Department of Forensic Medicine and Toxicology, Medical School, University of Athens, Greece
Author contributions: All authors contributed equally to the work.
Correspondence to: John Griniatsos, MD, Lecturer in Surgery, 43 Tenedou Street, G.R. 113-61 Athens, Greece. johngrin@hotmail.com
Telephone: +30-210-8624627 Fax: +30-210-7771195
Received: October 4, 2005
Revised: November 11, 2005
Accepted: November 18, 2005
Published online: April 7, 2006
Abstract

AIM: To evaluate whether the cellular proliferation rate in the large bowel epithelial cells is characterized by circadian rhythm.

METHODS: Between January 2003 and December 2004, twenty patients who were diagnosed as suffering from primary, resectable, non-metastatic adenocarcinoma of the lower rectum, infiltrating the sphincter mechanism, underwent abdominoperineal resection, total mesorectal excision and permanent left iliac colostomy. In formalin-fixed and paraffin-embedded biopsy specimens obtained from the colostomy mucosa every six hours (00:00, 06:00, 12:00, 18:00 and 24:00), we studied the expression of G1 phase cyclins (D1 and E) as well as the expression of the G1 phase cyclin-dependent kinase (CDK) inhibitors p16 and p21 as indicators of cell cycle progression in colonic epithelial cells using immunohistochemical methods.

RESULTS: The expression of both cyclins showed a similar circadian fashion obtaining their lowest and highest values at 00:00 and 18:00, respectively (P< 0.001). A circadian rhythm in the expression of CDK inhibitor proteins p16 and p21 was also observed, with the lowest levels obtained at 12:00 and 18:00 (P< 0.001), respectively. When the complexes cyclins D1 - p21 and E - p21 were examined, the expression of the cyclins was adversely correlated to the p21 expression throughout the day. When the complexes the cyclins D1 - p16 and E - p16 were examined, high levels of p16 expression were correlated to low levels of cyclin expression at 00:00, 06:00 and 24:00. Meanwhile, the highest expression levels of both cyclins were correlated to high levels of p16 expression at 18:00.

CONCLUSION: Colonic epithelial cells seem to enter the G1 phase of the cell cycle during afternoon (between 12:00 and 18:00) with the highest rates obtained at 18:00. From a clinical point of view, the present results suggest that G1-phase specific anticancer therapies in afternoon might maximize their anti-tumor effect while minimizing toxicity.

Keywords: G1 phase proteins; CDK inhibitors; Cell proliferation; Circadian rhythm