INCREASED LEVELS OF LUMINOL-ENHANCED CHEMILUMINESCENCE BY RECTAL MUCOSA OF PATIENTS WITH COLONIC NEOPLASIA - A POSSIBLE MARKER FOR COLONIC NEOPLASIA

Citation
A. Keshavarzian et al., INCREASED LEVELS OF LUMINOL-ENHANCED CHEMILUMINESCENCE BY RECTAL MUCOSA OF PATIENTS WITH COLONIC NEOPLASIA - A POSSIBLE MARKER FOR COLONIC NEOPLASIA, Nutrition and cancer, 19(2), 1993, pp. 201-206
Citations number
23
Categorie Soggetti
Nutrition & Dietetics",Oncology
Journal title
ISSN journal
01635581
Volume
19
Issue
2
Year of publication
1993
Pages
201 - 206
Database
ISI
SICI code
0163-5581(1993)19:2<201:ILOLCB>2.0.ZU;2-M
Abstract
Increased colonic cell proliferation (CCP) has been reported in patien ts with colonic neoplasia. Previous studies in rats suggest that incre ased CCP is closely related to increased reactive oxygen metabolite (R OM) production. We hypothesized that, in humans, ROM production is als o involved in increased CCP. Using a chemiluminescence probe, we estim ated the levels of ROMs in the rectal mucosa of 37 patients who previo usly had colonic neoplasia (14 with cancer and 23 with polyps) and 20 control subjects who had normal colonoscopic examination and no histor y of colonic neoplasia. Normal-appearing rectal mucosa of patients wit h colonic neoplasia contained significantly higher levels of luminol-e nhanced chemiluminescence (LECL) than rectal mucosa of control subject s (p < 0.01). There was no difference in LECL levels between patients with polyps and patients with cancer. Four of 20 controls and 31 of 37 patients had LECL levels 1,000 cpm/mg protein (positive and negative predictive values of 89% and 73%, respectively). Addition of indometha cin, a specific cyclooxygenase inhibitor, to the tissue suspension sig nificantly decreased LECL levels. These preliminary data suggest that 1) ROMs may be involved in both the rate of CCP and the process of mal ignant cellular transformation, 2) oxidation of arachidonic acid via t he cyclooxygenase pathway significantly contributes to the production of ROMs in rectal mucosa, and 3) measurement of the levels of LECL pro duced by the rectal mucosa may be a sensitive marker to screen for col onic neoplasia.