DNA microarray analysis of gene expression markers of endometriosis

被引:111
作者
Eyster, KM [1 ]
Boles, AL
Brannian, JD
Hansen, KA
机构
[1] Univ S Dakota, Sch Med, Div Basic Biomed Sci, Vermillion, SD 57069 USA
[2] Univ S Dakota, Sch Med, Dept Obstet & Gynecol, Vermillion, SD 57069 USA
关键词
endometriosis; endometrium; microarray; gene expression;
D O I
10.1016/S0015-0282(01)02955-7
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To use DNA microarray technology to examine differential gene expression in uterine endometrium versus endometriosis implants. Design: Pilot study. Setting: Volunteers in an academic research environment. Patient(s) Premenopausal women scheduled for surgery for suspected endometriosis. Intervention(s): Surgical excision of endometriosis tissue and uterine endometrial biopsy. Main Outcome Measure(s): Gene expression. Result(s): The expression of eight genes from a total of 4.133 genes on the DNA microarray was increased in endometriosis implants compared with uterine endometrium. The eight genes were beta-actin, alpha-2 actin, vimentin, 40S ribosomal protein S23. Ig-lambda light chain, Ig germline H chain G-E-A region gamma-2 constant region gene, major histocompatibility complex class 1.C, and complement component 1 S subcomponent. Conclusion(s): The data demonstrate that the DNA microarray is an effective tool for the identification of differentially expressed genes between uterine and ectopic endometrium;further study of the genes identified herein will expand our understanding of the nature of endometriosis and assist in the eventual development of new treatments for endometriosis. (Fertil Steril(R) 2002;77:38-42. (C) 2002 by American Society for Reproductive Medicine.).
引用
收藏
页码:38 / 42
页数:5
相关论文
共 23 条
[1]   Suppression of matrix metalloproteinases inhibits establishment of ectopic lesions by human endometrium in nude mice [J].
Bruner, KL ;
Matrisian, LM ;
Rodgers, WH ;
Gorstein, F ;
Osteen, KG .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (12) :2851-2857
[2]   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
[3]   Integrating the actin and vimentin cytoskeletons: Adhesion-dependent formation of fimbrin-vimentin complexes in macrophages [J].
Correia, I ;
Chu, D ;
Chou, YH ;
Goldman, RD ;
Matsudaira, P .
JOURNAL OF CELL BIOLOGY, 1999, 146 (04) :831-842
[4]  
Evans Robert M., 1994, Trends in Cell Biology, V4, P149, DOI 10.1016/0962-8924(94)90189-9
[5]  
Giudice LC, 1998, J REPROD MED, V43, P252
[6]  
GOLDSBY RA, 2000, KUBY IMMUNOLOGY, P115
[7]   The roles of calmodulin, actin, and vimentin in steroid synthesis by adrenal cells [J].
Hall, PF .
STEROIDS, 1997, 62 (01) :185-189
[8]   Intermediate filaments and their associates: multi-talented structural elements specifying cytoarchitecture and cytodynamics [J].
Herrmann, H ;
Aebi, U .
CURRENT OPINION IN CELL BIOLOGY, 2000, 12 (01) :79-90
[9]   Expression or aromatase cytochrome P450 protein and messenger ribonucleic acid in human endometriotic and adenomyotic tissues but not in normal endometrium [J].
Kitawaki, J ;
Noguchi, T ;
Amatsu, T ;
Maeda, K ;
Tsukamoto, K ;
Yamamoto, T ;
Fushiki, S ;
Osawa, Y ;
Honjo, H .
BIOLOGY OF REPRODUCTION, 1997, 57 (03) :514-519
[10]   INTERMEDIATE FILAMENTS - NEW PROTEINS, SOME ANSWERS, MORE QUESTIONS [J].
KLYMKOWSKY, MW .
CURRENT OPINION IN CELL BIOLOGY, 1995, 7 (01) :46-54