Common chromosomal imbalances and stemness-related protein expression markers in endometriotic lesions from different anatomical sites: the potential role of stem cells


Autoria(s): Silveira, Cassia G. T.; Abrao, Mauricio S.; Dias, Joao A., Jr.; Coudry, Renata A.; Soares, Fernando A.; Drigo, Sandra A.; Domingues, Maria A. C.; Rogatto, Silvia R.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

14/10/2013

14/10/2013

2012

Resumo

Endometriosis is a multifactorial gynecological disease characterized by the presence of functional endometrium-like tissue in ectopic sites. Several studies have focused on elucidating the immunological, endocrine, environmental and genetic factors involved in endometriosis. However, its pathogenesis is still unclear. High-resolution comparative genomic hybridization was applied to screen for genomic imbalances in laser microdissected stromal and epithelial cells from 20 endometriotic lesions and three samples of eutopic endometrium derived from eight patients. The expression of seven stemness-related markers (CD9, CD13, CD24, CD34, CD133, CD117/c-Kit and Oct-4) in endometrial tissue samples was evaluated by immunohistochemistry. Samples of eutopic endometrium showed normal genomic profiles. In ectopic tissues, an average of 68 genomic imbalances was detected per sample. DNA losses were more frequently detected and involved mainly 3p, 5q, 7p, 9p, 11q, 16q, 18q and 19q. Many of the genomic imbalances detected were common to endometriotic stroma and epithelia and also among different endometriotic sites from the same patient. These findings suggested a clonal origin of the endometriotic cells and the putative involvement of stem cells. Positive immunostaining for CD9, CD34, c-Kit and Oct-4 markers was detected in isolated epithelial and/or stromal cells in eutopic and ectopic endometrium in the majority of cases. The presence of shared genomic alterations in stromal and epithelial cells from different anatomical sites of the same patient and the expression of stemness-related markers suggested that endometriosis arises as a clonal proliferation with the putative involvement of stem cells.

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Identificador

HUMAN REPRODUCTION, OXFORD, v. 27, n. 11, supl. 1, Part 1, pp. 3187-3197, NOV, 2012

0268-1161

http://www.producao.usp.br/handle/BDPI/35050

10.1093/humrep/des282

http://dx.doi.org/10.1093/humrep/des282

Idioma(s)

eng

Publicador

OXFORD UNIV PRESS

OXFORD

Relação

HUMAN REPRODUCTION

Direitos

closedAccess

Copyright OXFORD UNIV PRESS

Palavras-Chave #ENDOMETRIOSIS #HIGH-RESOLUTION COMPARATIVE GENOMIC HYBRIDIZATION #CHROMOSOMAL IMBALANCES #PROTEIN EXPRESSION #STEM CELLS #COMPARATIVE GENOMIC HYBRIDIZATION #HUMAN HEMATOPOIETIC STEM #MOLECULAR-MECHANISMS #CYTOGENETIC ANALYSIS #MOUSE ENDOMETRIUM #WIDE ASSOCIATION #PERITONEAL-FLUID #EPITHELIAL-CELLS #AMINOPEPTIDASE-N #STROMAL CELLS #OBSTETRICS & GYNECOLOGY #REPRODUCTIVE BIOLOGY
Tipo

article

original article

publishedVersion