β-Catenin signaling regulates Foxa2 expression during endometrial hyperplasia formation

M. Villacorte, K. Suzuki, Akira Hirasawa, Y. Ohkawa, M. Suyama, T. Maruyama, D. Aoki, Y. Ogino, S. Miyagawa, T. Terabayashi, Y. Tomooka, N. Nakagata, G. Yamada

Research output: Contribution to journalArticle

29 Citations (Scopus)

Abstract

The Wnt/β-catenin signaling is essential for various organogenesis and is often implicated during tumorigenesis. Dysregulated β-catenin signaling is associated with the formation of endometrial adenocarcinomas (EACs), which is considered as the common form of endometrial cancer in women. In the current study, we investigate the downstream target of Wnt/β-catenin signaling in the uterine epithelia and the mechanism leading to the formation of endometrial hyperplasia. We report that conditional ablation and activation of β-catenin in the uterine epithelia lead to aberrant epithelial structures and endometrial hyperplasia formation, respectively. We demonstrate that β-catenin regulates Foxa2 with its candidate upstream region for the uterine epithelia. Furthermore, knockdown of Foxa2 leads to defects in cell cycle regulation, suggesting a possible function of Foxa2 in the control of cell proliferation. We also observe that β-catenin and Foxa2 expression levels are augmented in the human specimens of complex atypical endometrial hyperplasia, which is considered to have a greater risk of progression to EACs. Thus, our study indicates that β-catenin regulates Foxa2 expression, and this interaction is possibly essential to control cell cycle progression during endometrial hyperplasia formation. Altogether, the augmented expression levels of β-catenin and Foxa2 are essential features during the formation of endometrial hyperplasia.

Original languageEnglish
Pages (from-to)3477-3482
Number of pages6
JournalOncogene
Volume32
Issue number29
DOIs
Publication statusPublished - Jul 18 2013
Externally publishedYes

Fingerprint

Endometrial Hyperplasia
Catenins
Epithelium
Adenocarcinoma
Organogenesis
Endometrial Neoplasms
Cell Cycle Checkpoints
Cell Cycle
Carcinogenesis
Cell Proliferation

Keywords

  • Cyclin
  • Endometrial hyperplasia
  • Foxa2
  • Uterine gland
  • Wnt/β-catenin

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cancer Research

Cite this

Villacorte, M., Suzuki, K., Hirasawa, A., Ohkawa, Y., Suyama, M., Maruyama, T., ... Yamada, G. (2013). β-Catenin signaling regulates Foxa2 expression during endometrial hyperplasia formation. Oncogene, 32(29), 3477-3482. https://doi.org/10.1038/onc.2012.376

β-Catenin signaling regulates Foxa2 expression during endometrial hyperplasia formation. / Villacorte, M.; Suzuki, K.; Hirasawa, Akira; Ohkawa, Y.; Suyama, M.; Maruyama, T.; Aoki, D.; Ogino, Y.; Miyagawa, S.; Terabayashi, T.; Tomooka, Y.; Nakagata, N.; Yamada, G.

In: Oncogene, Vol. 32, No. 29, 18.07.2013, p. 3477-3482.

Research output: Contribution to journalArticle

Villacorte, M, Suzuki, K, Hirasawa, A, Ohkawa, Y, Suyama, M, Maruyama, T, Aoki, D, Ogino, Y, Miyagawa, S, Terabayashi, T, Tomooka, Y, Nakagata, N & Yamada, G 2013, 'β-Catenin signaling regulates Foxa2 expression during endometrial hyperplasia formation', Oncogene, vol. 32, no. 29, pp. 3477-3482. https://doi.org/10.1038/onc.2012.376
Villacorte M, Suzuki K, Hirasawa A, Ohkawa Y, Suyama M, Maruyama T et al. β-Catenin signaling regulates Foxa2 expression during endometrial hyperplasia formation. Oncogene. 2013 Jul 18;32(29):3477-3482. https://doi.org/10.1038/onc.2012.376
Villacorte, M. ; Suzuki, K. ; Hirasawa, Akira ; Ohkawa, Y. ; Suyama, M. ; Maruyama, T. ; Aoki, D. ; Ogino, Y. ; Miyagawa, S. ; Terabayashi, T. ; Tomooka, Y. ; Nakagata, N. ; Yamada, G. / β-Catenin signaling regulates Foxa2 expression during endometrial hyperplasia formation. In: Oncogene. 2013 ; Vol. 32, No. 29. pp. 3477-3482.
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