Genetic determinants of FOXM1 overexpression in epithelial ovarian cancer and functional contribution to cell cycle progression

Carter J. Barger, Wa Zhang, Joanna Hillman, Aimee B. Stablewski, Michael J. Higgins, Barbara C. Vanderhyden, Kunle Odunsi, Adam R Karpf

Research output: Contribution to journalArticle

30 Citations (Scopus)

Abstract

The FOXM1 transcription factor network is frequently activated in high-grade serous ovarian cancer (HGSOC), the most common and lethal subtype of epithelial ovarian cancer (EOC). We used primary human EOC tissues, HGSOC cell lines, mouse and human ovarian surface epithelial (OSE) cells, and a murine transgenic ovarian cancer model to investigate genetic determinants of FOXM1 overexpression in EOC, and to begin to define its functional contribution to disease pathology. The Cancer Genome Atlas (TCGA) data indicated that the FOXM1 locus is amplified in ~12% of HGSOC, greater than any other tumor type examined, and that FOXM1 amplification correlates with increased expression and poor survival. In an independent set of primary EOC tissues, FOXM1 expression correlated with advanced stage and grade. Of the three known FOXM1 isoforms, FOXM1c showed highest expression in EOC. In murine OSE cells, combined knockout of Rb1 and Trp53 synergistically induced FOXM1. Consistently, human OSE cells immortalized with SV40 Large T antigen (IOSE-SV) had significantly higher FOXM1 expression than OSE immortalized with hTERT (IOSE-T). FOXM1 was overexpressed in murine ovarian tumors driven by combined Rb1/Trp53 disruption. FOXM1 induction in IOSE-SV cells was partially dependent on E2F1, and FOXM1 expression correlated with E2F1 expression in human EOC tissues. Finally, FOXM1 functionally contributed to cell cycle progression and relevant target gene expression in human OSE and HGSOC cell models. In summary, gene amplification, p53 and Rb disruption, and E2F1 activation drive FOXM1 expression in EOC, and FOXM1 promotes cell cycle progression in EOC cell models.

Original languageEnglish (US)
Pages (from-to)27613-27627
Number of pages15
JournalOncotarget
Volume6
Issue number29
DOIs
StatePublished - 2015

Fingerprint

Cell Cycle
Ovarian Neoplasms
Epithelial Cells
Polyomavirus Transforming Antigens
Neoplasms
Ovarian epithelial cancer
Gene Amplification
Atlases
Viral Tumor Antigens
Protein Isoforms
Transcription Factors
Genome
Pathology
Gene Expression
Cell Line
Survival

Keywords

  • E2F1
  • Epithelial ovarian cancer
  • FOXM1
  • p53
  • Rb

ASJC Scopus subject areas

  • Oncology

Cite this

Genetic determinants of FOXM1 overexpression in epithelial ovarian cancer and functional contribution to cell cycle progression. / Barger, Carter J.; Zhang, Wa; Hillman, Joanna; Stablewski, Aimee B.; Higgins, Michael J.; Vanderhyden, Barbara C.; Odunsi, Kunle; Karpf, Adam R.

In: Oncotarget, Vol. 6, No. 29, 2015, p. 27613-27627.

Research output: Contribution to journalArticle

Barger, CJ, Zhang, W, Hillman, J, Stablewski, AB, Higgins, MJ, Vanderhyden, BC, Odunsi, K & Karpf, AR 2015, 'Genetic determinants of FOXM1 overexpression in epithelial ovarian cancer and functional contribution to cell cycle progression', Oncotarget, vol. 6, no. 29, pp. 27613-27627. https://doi.org/10.18632/oncotarget.4546
Barger, Carter J. ; Zhang, Wa ; Hillman, Joanna ; Stablewski, Aimee B. ; Higgins, Michael J. ; Vanderhyden, Barbara C. ; Odunsi, Kunle ; Karpf, Adam R. / Genetic determinants of FOXM1 overexpression in epithelial ovarian cancer and functional contribution to cell cycle progression. In: Oncotarget. 2015 ; Vol. 6, No. 29. pp. 27613-27627.
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abstract = "The FOXM1 transcription factor network is frequently activated in high-grade serous ovarian cancer (HGSOC), the most common and lethal subtype of epithelial ovarian cancer (EOC). We used primary human EOC tissues, HGSOC cell lines, mouse and human ovarian surface epithelial (OSE) cells, and a murine transgenic ovarian cancer model to investigate genetic determinants of FOXM1 overexpression in EOC, and to begin to define its functional contribution to disease pathology. The Cancer Genome Atlas (TCGA) data indicated that the FOXM1 locus is amplified in ~12{\%} of HGSOC, greater than any other tumor type examined, and that FOXM1 amplification correlates with increased expression and poor survival. In an independent set of primary EOC tissues, FOXM1 expression correlated with advanced stage and grade. Of the three known FOXM1 isoforms, FOXM1c showed highest expression in EOC. In murine OSE cells, combined knockout of Rb1 and Trp53 synergistically induced FOXM1. Consistently, human OSE cells immortalized with SV40 Large T antigen (IOSE-SV) had significantly higher FOXM1 expression than OSE immortalized with hTERT (IOSE-T). FOXM1 was overexpressed in murine ovarian tumors driven by combined Rb1/Trp53 disruption. FOXM1 induction in IOSE-SV cells was partially dependent on E2F1, and FOXM1 expression correlated with E2F1 expression in human EOC tissues. Finally, FOXM1 functionally contributed to cell cycle progression and relevant target gene expression in human OSE and HGSOC cell models. In summary, gene amplification, p53 and Rb disruption, and E2F1 activation drive FOXM1 expression in EOC, and FOXM1 promotes cell cycle progression in EOC cell models.",
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