Whole genome deoxyribonucleic acid microarray analysis of gene expression in ectopic versus eutopic endometrium

被引:135
作者
Eyster, Kathleen M. [1 ,2 ]
Klinkova, Olga [1 ]
Kennedy, Vanessa [1 ]
Hansen, Keith A. [2 ,3 ,4 ]
机构
[1] Univ S Dakota, Sanford Sch Med, Div Basic Biomed Sci, Vermillion, SD 57069 USA
[2] Univ S Dakota, Sanford Sch Med, Womens Hlth Res Ctr, Sioux Falls, SD USA
[3] Univ S Dakota, Sanford Sch Med, Dept Obstet & Gynecol, Sioux Falls, SD USA
[4] Univ S Dakota, Sanford Sch Med, Sioux Valley Hosp, Med Ctr, Sioux Falls, SD USA
关键词
endometriosis; differential gene expression; DNA microarray; phospholipase A(2);
D O I
10.1016/j.fertnstert.2007.01.056
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To use DNA microarrays to identify differentially expressed genes in eutopic endometrium compared with ectopic endometrium. Design: Prospective, cross-sectional, observational study. Setting: University Medical Center and Research Laboratory. Patient(s): Eleven women with endometriosis. Intervention(S): None. Main Outcome Measure(s): Differential gene expression. Result(s): Seven hundred seventeen of the 53,000 probes on the whole human DNA microarrays were changed by twofold or greater in ectopic versus eutopic endometrium. Families of genes that were expressed differentially include genes that code for proteins associated with the immune system and inflammatory pathways, cell adhesion, cell-cell junctions, the extracellular matrix and its remodeling, cytoskeletal proteins, and signal transduction pathway components, among others. Conclusion(S): The altered immune environment may allow survival of endometriotic cells that enter the abdominal cavity. Alterations of cell adhesion-associated genes may contribute to the adhesive and invasive properties of ectopic endometrium, and changes in signal transduction pathways support a change in the communication among cells of the endometrial explant compared with eutopic endometrium. These fan-Lilies of differentially expressed genes provide multiple opportunities for the development and testing of new hypotheses regarding endometriosis. (Fertil Steril((R)) 2007;88:1505-33. (c) 2007 by American Society for Reproductive Medicine.)
引用
收藏
页码:1505 / 1533
页数:29
相关论文
共 53 条
[1]  
Arimoto T, 2003, INT J ONCOL, V22, P551
[2]   Potentiation of tumor necrosis factor α-induced secreted phospholipase A2 (sPLA2)-IIA expression in mesangial cells by an autocrine loop involving sPLA2 and peroxisome proliferator-activated receptor α activation [J].
Beck, S ;
Lambeau, G ;
Scholz-Pedretti, K ;
Gelb, MH ;
Janssen, MJW ;
Edwards, SH ;
Wilton, DC ;
Pfeilschifter, J ;
Kaszkin, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (32) :29799-29812
[3]   Variant glycosylation:: an underappreciated regulatory mechanism for β1 integrins [J].
Bellis, SL .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2004, 1663 (1-2) :52-60
[4]   Analysis of the role of chemokines in angiogenesis [J].
Bernardini, G ;
Ribatti, D ;
Spinetti, G ;
Morbidelli, L ;
Ziche, M ;
Santoni, A ;
Capogrossi, MC ;
Napolitano, M .
JOURNAL OF IMMUNOLOGICAL METHODS, 2003, 273 (1-2) :83-101
[5]   Axis of evil: molecular mechanisms of cancer metastasis [J].
Bogenrieder, T ;
Herlyn, M .
ONCOGENE, 2003, 22 (42) :6524-6536
[6]   Minimum information about a microarray experiment (MIAME) - toward standards for microarray data [J].
Brazma, A ;
Hingamp, P ;
Quackenbush, J ;
Sherlock, G ;
Spellman, P ;
Stoeckert, C ;
Aach, J ;
Ansorge, W ;
Ball, CA ;
Causton, HC ;
Gaasterland, T ;
Glenisson, P ;
Holstege, FCP ;
Kim, IF ;
Markowitz, V ;
Matese, JC ;
Parkinson, H ;
Robinson, A ;
Sarkans, U ;
Schulze-Kremer, S ;
Stewart, J ;
Taylor, R ;
Vilo, J ;
Vingron, M .
NATURE GENETICS, 2001, 29 (04) :365-371
[7]   Estrogen production and metabolism in endometriosis [J].
Bulun, SE ;
Yang, SJ ;
Fang, ZJ ;
Gurates, B ;
Tamura, M ;
Sebastian, S .
ENDOMETRIOSIS: EMERGING RESEARCH AND INTERVENTION STRATEGIES, 2002, 955 :75-88
[8]   Bone morphogenetic proteins, their antagonists, and the skeleton [J].
Canalis, E ;
Economides, AN ;
Gazzerro, E .
ENDOCRINE REVIEWS, 2003, 24 (02) :218-235
[9]  
Canis M, 1997, FERTIL STERIL, V67, P817
[10]   Role of K-ras and Pten in the development of mouse models of endometriosis and endometrioid ovarian cancer [J].
Dinulescu D.M. ;
Ince T.A. ;
Quade B.J. ;
Shafer S.A. ;
Crowley D. ;
Jacks T. .
Nature Medicine, 2005, 11 (1) :63-70