In vivo analysis of progesterone receptor action in the uterus during embryo implantation

被引:103
作者
Franco, Heather L. [1 ]
Jeong, Jae-Wook [1 ]
Tsai, Sophia Y. [1 ]
Lydon, John P. [1 ]
DeMayo, Francesco J. [1 ]
机构
[1] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
关键词
progesterone receptor; uterus; endometriosis; endometrial cancer;
D O I
10.1016/j.semcdb.2007.12.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
In order for a successful pregnancy to occur, the embryo must attach to the luminal epithelial cells and invade into the stroma. Then, the surrounding stromal cells need to undergo decidualization in order to establish the vasculature necessary for survival of the embryo. These events in early pregnancy are tightly regulated by the steroid hormones, estrogen (E2) and progesterone (P4), through their cognate receptors, the estrogen receptor (ER) and the progesterone receptor (PR), respectively. Using a mouse model in which the PR has been ablated, it was demonstrated that the PR is necessary for embryo implantation and decidualization. Therefore, understanding the mechanism of PR action in the adult uterus is necessary in order to understand the events of early pregnancy. Insights from both mouse models and human samples have been integral in elucidating uterine PR action. These studies have shown that not only PR target genes, but also mediators of PR action are important for correct PR action in early pregnancy. Many of the genes involved in PR action in early pregnancy have also been shown to have roles in uterine diseases such as endometriosis and endometrial cancer. Therefore, the integration of mouse and human studies on PR action in the uterus will be important for the future understanding of uterine diseases and in the development of treatment for these diseases. (C) 2008 Published by Elsevier Ltd.
引用
收藏
页码:178 / 186
页数:9
相关论文
共 84 条
[1]
Benson GV, 1996, DEVELOPMENT, V122, P2687
[2]
Progesterone resistance in endometriosis: Link to failure to metabolize estradiol [J].
Bulun, SE ;
Cheng, YH ;
Yin, P ;
Imir, G ;
Utsunomiya, H ;
Attar, E ;
Innes, J ;
Kim, JJ .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2006, 248 (1-2) :94-103
[3]
Gene expression analysis of endometrium reveals progesterone resistance and candidate susceptibility genes in women with endometriosis [J].
Burney, Richard O. ;
Talbi, Said ;
Hamilton, Amy E. ;
Vo, Kim Chi ;
Nyegaard, Mette ;
Nezhat, Camran R. ;
Lessey, Bruce A. ;
Giudice, Linda C. .
ENDOCRINOLOGY, 2007, 148 (08) :3814-3826
[4]
Embryo implantation [J].
Carson, DD ;
Bagchi, I ;
Dey, SK ;
Enders, AC ;
Fazleabas, AT ;
Lessey, BA ;
Yoshinaga, K .
DEVELOPMENTAL BIOLOGY, 2000, 223 (02) :217-237
[5]
Chakrabarty A, 2007, P NATL ACAD SCI USA, V104, P15144, DOI 10.1073/pnas.0705917104
[6]
Progesterone inhibits the estrogen-induced phosphoinositide 3-Kinase→AKT→GSK-β3→Cyclin D1→pRB pathway to block uterine epithelial cell proliferation [J].
Chen, B ;
Pan, HY ;
Zhu, LY ;
Deng, Y ;
Pollard, JW .
MOLECULAR ENDOCRINOLOGY, 2005, 19 (08) :1978-1990
[7]
Loss of cyclooxygenase-2 retards decidual growth but does not inhibit embryo implantation or development to term [J].
Cheng, JG ;
Stewart, CL .
BIOLOGY OF REPRODUCTION, 2003, 68 (02) :401-404
[8]
A genomic approach to identify novel progesterone receptor regulated pathways in the uterus during implantation [J].
Cheon, YP ;
Li, QX ;
Xu, XP ;
Demayo, FJ ;
Bagchi, IC ;
Bagchi, MK .
MOLECULAR ENDOCRINOLOGY, 2002, 16 (12) :2853-2871
[9]
Reproductive functions of the progesterone receptor isoforms: lessons from knock-out mice [J].
Conneely, OM ;
Mulac-Jericevic, B ;
Lydon, JP ;
De Mayo, FJ .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2001, 179 (1-2) :97-103
[10]
Role of stromal-epithelial interactions in hormonal responses [J].
Cunha, GR ;
Cooke, PS ;
Kurita, T .
ARCHIVES OF HISTOLOGY AND CYTOLOGY, 2004, 67 (05) :417-434