Involvement of FKHR (FOXO1) transcription factor in human uterus leiomyoma growth

被引:10
作者
Kovacs, Kalman A. [1 ]
Lengyel, Ferenc [2 ]
Wilhelm, Ferenc [1 ]
Vertes, Zsuzsanna [2 ]
Sumegi, Balazs [3 ]
Vertes, Marietta [2 ]
机构
[1] Univ Pecs, Dept Obstet & Gynecol, Sch Med, H-7624 Pecs, Hungary
[2] Univ Pecs, Inst Physiol, Sch Med, H-7624 Pecs, Hungary
[3] Univ Pecs, Dept Biochem, Sch Med, H-7624 Pecs, Hungary
关键词
FOXO1; 14-3-3; gamma; proteins; nuclear/cytoplasmic shuttling; leiomyoma; myometrium; human uterus; ESTROGEN-RECEPTOR-ALPHA; DIFFERENTIAL EXPRESSION; UTERINE LEIOMYOMAS; PHOSPHORYLATION; MECHANISMS; AKT; MYOMETRIUM; ACTIVATION; PROTEINS; CANCER;
D O I
10.1016/j.fertnstert.2009.07.1670
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To study the expression of FOXO1 and pSer(256)-FOXO1 parallel to Akt and pSer(473)-Akt in leiomyoma compared with adjacent myometrium from human uteri. Design: Prospective study. Setting: University departments. Patient(s): Thirty-eight cyclic and 20 menopausal women who underwent hysterectomy for benign indications. Intervention(s): None. Main Outcome Measure(s): Western blot analyses were used for evaluation in leiomyoma and adjacent myometrium of Akt and pSer(473)-Akt, 14-3-3 gamma proteins and expression and subcellular distribution of FOXO1 and pSer(256)-FOXO1 during the menstrual cycle and at menopause. Result(s): The present study demonstrates the expression of FOXO1 and pSer(256)-FOXO1 at the tissue level in the human uterus leiomyoma and adjacent myometrium. The level of phosphorylated FOXO1 in leiomyoma was higher than in matched myometrium. The pSer(256)-FOXO1 in leiomyoma during menstrual phases was located mostly in the nuclear fraction comparison to that of the myometrium. The reason for this difference is presumably the simultaneously detected lower level of 14-3-3 protein. Conclusion(s): Abundant level of the phosphorylated FOXO1, its impaired nucleocytoplasmic shuttling, and the lowered expression of 14-3-3 protein in leiomyoma induces a shift in the cellular machinery toward a prosurvival execution program and thus presents a potential therapeutic target for treatment of leiomyoma. (Fertil Steril (R) 2010;94:1491-5. (C) 2010 by American Society for Reproductive Medicine.)
引用
收藏
页码:1491 / 1495
页数:5
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