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Forkhead box transcription factor, forkhead box A 1, shows negative association with lymph node status in endometrial cancer, and represses cell proliferation and migration of endometrial cancer cells
Author(s) -
Abe Yayoi,
Ijichi Nobuhiro,
Ikeda Kazuhiro,
Kayano Hidekazu,
HorieInoue Kuniko,
Takeda Satoru,
Inoue Satoshi
Publication year - 2012
Publication title -
cancer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.035
H-Index - 141
eISSN - 1349-7006
pISSN - 1347-9032
DOI - 10.1111/j.1349-7006.2012.02201.x
Subject(s) - endometrial cancer , cancer research , foxa1 , estrogen receptor , biology , transcription factor , cancer , breast cancer , medicine , foxa2 , endocrinology , gene , biochemistry
Endometrial cancer is the most common malignancy of the female genital tract and is associated with poor prognosis. It is primarily a hormone‐dependent cancer that is regulated by steroid hormones, including estrogen and progesterone. Forkhead box A 1 ( FOXA 1) is a member of the forkhead box transcription factor family and functions as a pioneer factor in estrogen receptor ( ER )‐positive breast cancer. In the present study, we investigated the expression of FOXA 1 in endometrial cancers by immunohistochemical analysis. Nuclear immunoreactivity for FOXA 1 was detected in 40 of 109 cases (37%), and was found to be negatively associated with lymph node status ( P  = 0.033). In ER ‐positive I shikawa endometrial cancer cells, small interfering RNA ‐mediated downregulation of FOXA 1 promoted cell proliferation and migration. Furthermore, exogenously introduced FOXA 1 suppressed both proliferation and migration of I shikawa cells. These results suggest that FOXA 1 functions as a tumor suppressor through modulation of proliferation and migration of endometrial cancer cells. ( Cancer Sci 2012; 103: 806–812)

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