FOXA1: Growth inhibitor and a favorable prognostic factor in human breast cancer

Ido Wolf, Shikha Bose, Elizabeth A. Williamson, Carl W. Miller, Beth Y. Karlan, H. Phillip Koeffler

Research output: Contribution to journalArticlepeer-review

86 Scopus citations

Abstract

The transcription factor Forkhead-box A1 (Foxa1), a member of the FOX class of transcription factors, has been implicated in the pathogenesis of lung, esophageal and prostate cancers. We have recently identified transcriptional activation of p27 by FOXA1. In this study, we analyzed the activities and expression pattern of FOXA1 in breast cancer. Forced expression of FOXA1 inhibited clonal growth of breast cancer cell lines, and FOXA1 levels inversely correlated with growth stimuli. In the estrogen receptor (ER)-positive MCF-7 cells, FOXA1 increased p27 promoter activity and inhibited the ER pathway activity. Analysis of FOXA1 expression in breast tissue arrays revealed significantly higher expression in pure ductal carcinomas in situ compared to invasive ductal carcinomas (IDC); and in IDC, high expression of FOXA1 was associated with favorable prognostic factors. Yet, FOXA1 expression was noted in a subset of the ER-negative tumors. Taken together, our findings suggest a growth inhibitory role for FOXA1, and identify it as a novel, potential prognostic factor in breast cancer.

Original languageEnglish (US)
Pages (from-to)1013-1022
Number of pages10
JournalInternational Journal of Cancer
Volume120
Issue number5
DOIs
StatePublished - Mar 1 2007
Externally publishedYes

Keywords

  • Breast cancer
  • Estrogen receptor
  • FOXA1
  • p27

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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