Cyr61, a deregulated gene in endometriosis

被引:72
作者
Absenger, Y
Hess-Stumpp, H
Kreft, B
Krätzschmar, J
Haendler, B
Schütze, N
Regidor, PA
Winterhager, E [1 ]
机构
[1] Univ Hosp, Inst Anat, D-45122 Essen, Germany
[2] Schering AG, Res Labs, D-13342 Berlin, Germany
[3] Univ Wurzburg, Dept Orthopaed, D-97074 Wurzburg, Germany
[4] Univ Hosp, Dept Gynaecol, D-49076 Osnabruck, Germany
关键词
Cyr61; endometriosis; estrogen; human endometrium; microarray;
D O I
10.1093/molehr/gah053
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Gene expression profiling was performed to identify genes involved in the development of endometriosis. In the secretory phase of the menstrual cycle, several estrogen-regulated genes were up-regulated in endometria of women with endometriosis. The most consistent regulation with one of the highest factors was observed for the Cyr61 gene, which codes for a secreted, cysteine-rich, heparin-binding protein that promotes cell adhesion, migration, and neovascularization. Estrogen responsiveness of endometrial Cyr61 expression was suggested by the higher expression during the proliferative phase and the reduction observed in human endometrial fragments grafted into nude mice subsequently treated with an anti-estrogen. The expression level of Cyr61 was found to be further increased in ectopic endometriotic lesions, as compared to eutopic endometria. In these lesions, an imbalance in expression of the estrogen-converting enzymes 17beta-hydroxysteroid dehydrogenase type 1 and 2 was found, which might explain the elevated Cyr61 level. However, Cyr61 expression was not altered in endometriotic lesions of women treated with a GnRH agonist. These results suggest that Cyr61 may represent a gene characteristic for endometriosis and also play an important role in the development and persistence of endometriotic lesions.
引用
收藏
页码:399 / 407
页数:9
相关论文
共 49 条
[1]  
Akoum A, 1996, FERTIL STERIL, V66, P17
[2]   Tibolone: a review [J].
Albertazzi, P ;
Di Micco, R ;
Zanardi, E .
MATURITAS, 1998, 30 (03) :295-305
[3]  
Babic AM, 1999, MOL CELL BIOL, V19, P2958
[4]   CYR61, a product of a growth factor-inducible immediate early gene, promotes angiogenesis and tumor growth [J].
Babic, AM ;
Kireeva, ML ;
Kolesnikova, TV ;
Lau, LF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (11) :6355-6360
[5]   Effect of endometriosis on in vitro fertilization [J].
Barnhart, K ;
Dunsmoor-Su, R ;
Coutifaris, C .
FERTILITY AND STERILITY, 2002, 77 (06) :1148-1155
[6]   Localization of laminin, fibronectin, E-cadherin, and integrins in endometrium and endometriosis [J].
Beliard, A ;
Donnez, J ;
Nisolle, M ;
Foidart, JM .
FERTILITY AND STERILITY, 1997, 67 (02) :266-272
[7]   THE MODULAR ARCHITECTURE OF A NEW FAMILY OF GROWTH-REGULATORS RELATED TO CONNECTIVE-TISSUE GROWTH-FACTOR [J].
BORK, P .
FEBS LETTERS, 1993, 327 (02) :125-130
[8]   The connective tissue growth factor cysteine-rich 61 nephroblastoma overexpressed (CCN) family [J].
Brigstock, DR .
ENDOCRINE REVIEWS, 1999, 20 (02) :189-206
[9]   17-BETA-HYDROXYSTEROID DEHYDROGENASE TYPE-2 - CHROMOSOMAL ASSIGNMENT AND PROGESTIN REGULATION OF GENE-EXPRESSION IN HUMAN ENDOMETRIUM [J].
CASEY, ML ;
MACDONALD, PC ;
ANDERSSON, S .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (05) :2135-2141
[10]   TRANSCRIPTIONAL ACTIVATION OF JUN AND ACTIN GENES BY ESTROGEN DURING MITOGENIC STIMULATION OF RAT UTERINE CELLS [J].
CICATIELLO, L ;
AMBROSINO, C ;
COLETTA, B ;
SCALONA, M ;
SICA, V ;
BRESCIANI, F ;
WEISZ, A .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1992, 41 (3-8) :523-528