Differentially expressed genes in eutopic and ectopic endometrium of women with endometriosis


Autoria(s): MEOLA, Juliana; SILVA, Julio Cesar Rosa e; DENTILLO, Daniel Blassioli; SILVA JR., Wilson Araujo da; VEIGA-CASTELLI, Luciana Caricati; BERNARDES, Luciano Angelo de Souza; FERRIANI, Rui Alberto; PAZ, Claudia Cristina Paro de; GIULIATTI, Silvana; MARTELLI, Lucia
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2010

Resumo

Objective: To elucidate the potential mechanisms involved in the physiopathology of endometriosis. We analyzed the differential gene expression profiles of eutopic and ectopic tissues from women with endometriosis. Design: Prospective laboratory study. Setting: University hospital. Patient(s): Seventeen patients in whom endometriosis was diagnosed and 11 healthy fertile women. Intervention(s): Endometrial biopsy specimens from the endometrium of healthy women without endometriosis and from the eutopic and ectopic endometrium tissues of patients with endometriosis were obtained in the early proliferative phase of the menstrual cycle. Main Outcome Measure(s): Six paired samples of eutopic and ectopic tissue were analyzed by subtractive hybridization. To evaluate the expression of genes found by rapid subtraction hybridization methods, we measured CTGF, SPARC, MYC, MMP and IGFBP1 genes by real-time polymerase chain reaction in all samples. Result(s): This study identified 291 deregulated genes in the endometriotic lesions. Significant expression differences were obtained for SPARC, MYC, and IGFBP1 in the peritoneal lesions and for MMP3 in the ovarian endometriomas. Additionally, significant differences were obtained for SPARC and IGFBP1 between the peritoneal and ovarian lesions. No significant differences were found for the studied genes between the control and the eutopic endometrium. Conclusion(s): This study identified 291 genes with differential expression in endometriotic lesions. The deregulation of the SPARC, MYC, MMP3, and IGFBP1 genes may be responsible for the loss of cellular homeostasis in endometriotic lesions. (Fertil Steril(R) 2010;93:1750-73. (C) 2010 by American Society for Reproductive Medicine.)

Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES/PROEX), Brasilia, Brazil

Fundagao de Apoio ao Ensino, Pesquisa e Assistencia (FAEPA/HCFMRP-USP), Ribeirao Preto, Brazil

Identificador

FERTILITY AND STERILITY, v.93, n.6, p.1750-1773, 2010

0015-0282

http://producao.usp.br/handle/BDPI/24461

10.1016/j.fertnstert.2008.12.058

http://dx.doi.org/10.1016/j.fertnstert.2008.12.058

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE INC

Relação

Fertility and Sterility

Direitos

restrictedAccess

Copyright ELSEVIER SCIENCE INC

Palavras-Chave #Differential gene expression #endometriosis #endometrium #subtractive hybridization #COMPARATIVE GENOMIC HYBRIDIZATION #TISSUE GROWTH-FACTOR #C-MYC #OVARIAN ENDOMETRIOSIS #MICROARRAY ANALYSIS #MATRIX-METALLOPROTEINASES #UTERINE ENDOMETRIUM #ENDOTHELIAL-CELLS #PERITONEAL-FLUID #BREAST-CANCER #Obstetrics & Gynecology #Reproductive Biology
Tipo

article

original article

publishedVersion