Show simple item record

dc.contributor.authorSilveira, Cassia G. T. [UNESP]
dc.contributor.authorAbrao, Mauricio S.
dc.contributor.authorDias, Joao A.
dc.contributor.authorCoudry, Renata A.
dc.contributor.authorSoares, Fernando A.
dc.contributor.authorLinde, Sandra Aparecida Drigo [UNESP]
dc.contributor.authorDomingues, Maria Aparecida Custódio [UNESP]
dc.contributor.authorRogatto, Silvia Regina [UNESP]
dc.date.accessioned2014-05-20T13:37:35Z
dc.date.available2014-05-20T13:37:35Z
dc.date.issued2012-11-01
dc.identifierhttp://dx.doi.org/10.1093/humrep/des282
dc.identifier.citationHuman Reproduction. Oxford: Oxford Univ Press, v. 27, n. 11, p. 3187-3197, 2012.
dc.identifier.issn0268-1161
dc.identifier.urihttp://hdl.handle.net/11449/13031
dc.description.abstractEndometriosis 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.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.format.extent3187-3197
dc.language.isoeng
dc.publisherOxford University Press
dc.relation.ispartofHuman Reproduction
dc.sourceWeb of Science
dc.subjectendometriosisen
dc.subjecthigh-resolution comparative genomic hybridizationen
dc.subjectchromosomal imbalancesen
dc.subjectprotein expressionen
dc.subjectstem cellsen
dc.titleCommon chromosomal imbalances and stemness-related protein expression markers in endometriotic lesions from different anatomical sites: the potential role of stem cellsen
dc.typeArtigo
dcterms.licensehttp://www.oxfordjournals.org/access_purchase/self-archiving_policyb1.html
dcterms.rightsHolderOxford Univ Press
dc.contributor.institutionHosp AC Camargo Fund Antonio Prudente
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionSirio Libanes Hosp
dc.description.affiliationHosp AC Camargo Fund Antonio Prudente, Fundação Antonio Prudente, CIPE, NeoGene Lab,Dept Res, BR-01508010 São Paulo, Brazil
dc.description.affiliationSão Paulo State Univ, UNESP, Inst Biosci, Dept Genet, Botucatu, SP, Brazil
dc.description.affiliationUniv São Paulo, Dept Obstet & Gynecol, São Paulo, Brazil
dc.description.affiliationSirio Libanes Hosp, São Paulo, Brazil
dc.description.affiliationUNESP, NeoGene Lab, Fac Med, Dept Urol, Botucatu, SP, Brazil
dc.description.affiliationUNESP, Fac Med, Dept Pathol, Botucatu, SP, Brazil
dc.description.affiliationUnespSão Paulo State Univ, UNESP, Inst Biosci, Dept Genet, Botucatu, SP, Brazil
dc.description.affiliationUnespUNESP, NeoGene Lab, Fac Med, Dept Urol, Botucatu, SP, Brazil
dc.description.affiliationUnespUNESP, Fac Med, Dept Pathol, Botucatu, SP, Brazil
dc.identifier.doi10.1093/humrep/des282
dc.identifier.wosWOS:000310218300008
dc.rights.accessRightsAcesso restrito
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt
dc.identifier.lattes2259986546265579
unesp.author.lattes2259986546265579]|
unesp.author.orcid0000-0003-1647-7842[5]
unesp.author.orcid0000-0002-0932-7769[1]
dc.relation.ispartofjcr4.990
dc.relation.ispartofsjr2,643
Localize o texto completo

Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record