Large-scale gene expression studies of the endometrium: what have we learnt?

被引:26
作者
Sherwin, Rob
Catalano, Rob
Sharkey, Andrew
机构
[1] Rosie Hosp, Dept Obstet & Gynaecol, Cambridge CB2 2SW, England
[2] Univ Cambridge, Dept Pathol, Cambridge CB2 1QP, England
关键词
D O I
10.1530/rep.1.00355
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The endometrium is a dynamic tissue that undergoes coordinated changes under the influence of steroid hormones. This results in proliferation and differentiation culminating in a receptive state, followed by menstruation and endometrial repair. These functions involve complex interactions between the epithelium, stroma and leucocytes in the endometrium. Understanding the underlying causes of endometrial disorders, such as infertility, endometriosis and heavy menstrual bleeding, therefore represents a considerable challenge. Recently developed techniques, such as differential display and DNA microarrays permit the abundance of thousands of mRNA transcripts within cells or tissues to be measured simultaneously. This provides a new approach to understanding the complex interactions that underlie both healthy and disease states. Responses of the endometrium to hormones or drugs can be studied and the response of the system as an integrated whole can be assessed. Comparisons of endometrium from healthy women and those with endometrial dysfunction have advanced our understanding of key areas of endometrial physiology, including infertility, receptivity, endometriosis and cancer. Using this approach, novel genes controlling specific endometrial functions like receptivity have been identified for functional testing. This paper will review the impact of these techniques for transcript profiling on our understanding of selected areas of endometrial biology and discuss the potential applications in future.
引用
收藏
页码:1 / 10
页数:10
相关论文
共 69 条
[21]   A QUANTITATIVE ASSAY FOR DNA-RNA HYBRIDS WITH DNA IMMOBILIZED ON A MEMBRANE [J].
GILLESPIE, D ;
SPIEGELMAN, S .
JOURNAL OF MOLECULAR BIOLOGY, 1965, 12 (03) :829-+
[22]   The molecular basis for implantation failure in endometriosis - On the road to discovery [J].
Giudice, LC ;
Telles, TL ;
Lobo, S ;
Kao, L .
ENDOMETRIOSIS: EMERGING RESEARCH AND INTERVENTION STRATEGIES, 2002, 955 :252-264
[23]  
Holland CM, 2004, MOL CANCER THER, V3, P993
[24]   Expression profiling of endometrium from women with endometriosis reveals candidate genes for disease-based implantation failure and infertility [J].
Kao, LC ;
Germeyer, A ;
Tulac, S ;
Lobo, S ;
Yang, JP ;
Taylor, RN ;
Osteen, K ;
Lessey, BA ;
Giudice, LC .
ENDOCRINOLOGY, 2003, 144 (07) :2870-2881
[25]   Global gene profiling in human endometrium during the window of implantation [J].
Kao, LC ;
Tulac, S ;
Lobo, S ;
Imani, B ;
Yang, JP ;
Germeyer, A ;
Osteen, K ;
Taylor, RN ;
Lessey, BA ;
Giudice, LC .
ENDOCRINOLOGY, 2002, 143 (06) :2119-2138
[26]   Altered expression of a cell-cycle suppressor gene, Tob-1, in endometriotic cells by cDNA array analyses [J].
Lebovic, DI ;
Baldocchi, RA ;
Mueller, MD ;
Taylor, RN .
FERTILITY AND STERILITY, 2002, 78 (04) :849-854
[27]   A novel pathway involving progesterone receptor, 12/15-lipoxygenase-derived eicosanoids, and peroxisome proliferator-activated receptor γ regulates implantation in mice [J].
Li, QX ;
Cheon, YP ;
Kannan, A ;
Shanker, S ;
Bagchi, IC ;
Bagchi, MK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (12) :11570-11581
[28]   DIFFERENTIAL DISPLAY OF EUKARYOTIC MESSENGER-RNA BY MEANS OF THE POLYMERASE CHAIN-REACTION [J].
LIANG, P ;
PARDEE, AB .
SCIENCE, 1992, 257 (5072) :967-971
[29]   RECENT ADVANCES IN DIFFERENTIAL DISPLAY [J].
LIANG, P ;
PARDEE, AB .
CURRENT OPINION IN IMMUNOLOGY, 1995, 7 (02) :274-280
[30]   Endometrial calbindins are critical for embryo implantation:: Evidence from in vivo use of morpholino antisense oligonucleotides [J].
Luu, KC ;
Nie, GY ;
Salamonsen, LA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (21) :8028-8033