Celecoxib pre-treatment in human colorectal adenocarcinoma patients is associated with gene expression alterations suggestive of diminished cellular proliferation

  • James Todd Auman
  • , Robert Church
  • , Soo Youn Lee
  • , Mark A. Watson
  • , James W. Fleshman
  • , Howard L. Mcleod

Research output: Contribution to journalArticlepeer-review

26 Scopus citations

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 (400 mg 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.

Original languageEnglish
Pages (from-to)1754-1760
Number of pages7
JournalEuropean Journal of Cancer
Volume44
Issue number12
DOIs
StatePublished - Aug 2008

Keywords

  • Celecoxib
  • Colorectal neoplasms
  • Cyclooxygenase 2 inhibitors
  • Gene expression profiling
  • cDNA microarrays

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