Wild-type APC regulates caveolin-1 expression in human colon adenocarcinoma cell lines via FOXO1a and C-myc

Upal K.Basu Roy, Rebecca S. Henkhaus, Natalia A. Ignatenko, Jessica Mora, Kimberly E. Fultz, Eugene W. Gerner

Research output: Contribution to journalArticlepeer-review

29 Scopus citations


Genetic evidence suggests that caveolin-1, an essential component of membrane caveolae, acts as a tumor promoter in some, and a tumor suppressor in other cancers. The role of caveolin-1 in colon carcinogenesis is controversial. We report here, for the first time, that caveolin-1 is transcriptionally induced in colon cancer cells in response to conditional expression of a full length adenomatous polyposis coli (APC) gene. This induction of caveolin-1 by APC is mediated by both FOXO1a, a member of the Forkhead family of transcription factor, and c-myc. The FOXO1a protein, which is increased by wild-type APC expression, induces caveolin-1 promoter-reporter activity and binds directly to a FKHR consensus binding sequence in the caveolin-1 promoter. The c-myc protein, which is reduced in the presence of wild-type APC, acts to repress caveolin-1 expression by acting at non-E-box containing elements in the caveolin-1 promoter. These data predict that caveolin-1 protein expression would be decreased early in colonic carcinogenesis, which is associated with loss of wild-type APC. Our results would be consistent with the interpretation that caveolin-1 may have tumor suppressing functions during early stages of colon carcinogenesis.

Original languageEnglish (US)
Pages (from-to)947-955
Number of pages9
JournalMolecular Carcinogenesis
Issue number12
StatePublished - Dec 2008


  • APC
  • C-myc
  • Caveolin-1
  • Colon cancer

ASJC Scopus subject areas

  • Molecular Biology
  • Cancer Research


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