| Literature DB >> 18653328 |
James Todd Auman1, Robert Church, Soo-Youn Lee, Mark A Watson, James W Fleshman, Howard L Mcleod.
Abstract
Cancer cells treated with the cyclooxygenase-2 inhibitor celecoxib show growth inhibition and induced apoptosis. This study was conducted to determine if the same processes are relevant to celecoxib's effects on human colorectal adenocarcinomas treated in vivo. A cohort of 23 patients with primary colorectal adenocarcinomas was randomised to receive a 7-d course of celecoxib (400mg b.i.d.) or no drug prior to surgical resection. Gene expression profiling was performed on resected adenocarcinomas from the cohort of patients. Using fold change (>1.5) and p-value (<0.05) cut-offs, 190 genes were differentially expressed between adenocarcinomas from patients receiving celecoxib and those that did not. The celecoxib pre-treated samples showed decreased expression levels in multiple genes involved in cellular lipid and glutathione metabolism; changes associated with diminished cellular proliferation. Celecoxib pre-treatment for 7 d in vivo is associated with alterations in colorectal adenocarcinoma gene expression which are suggestive of diminished cellular proliferation.Entities:
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Year: 2008 PMID: 18653328 PMCID: PMC2566790 DOI: 10.1016/j.ejca.2008.05.010
Source DB: PubMed Journal: Eur J Cancer ISSN: 0959-8049 Impact factor: 9.162