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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

verexpression of miR-200b-3p in Menstrual Blood-Derived Mesenchymal Stem Cells from Endometriosis Wome

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Autor(es):
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de Oliveira, Rafael Zucco [1] ; Buono, Fabiana de Oliveira [1] ; Lagazzi Cressoni, Ana Clara [1] ; Correa Penariol, Leticia Bruna [1] ; Padovan, Cristiana Carolina [1] ; Tozetti, Patricia Aparecida [1] ; Poli-Neto, Omero Benedito [1, 2] ; Ferriani, Rui Alberto [1, 3] ; Orellana, Maristela Delgado [4, 5] ; Rosa-E-Silva, Julio Cesar [1, 2] ; Meola, Juliana [1, 2, 3]
Número total de Autores: 11
Afiliação do(s) autor(es):
[1] Univ Sao Paulo, Ribeirao Preto Med Sch, Dept Gynecol & Obstet, Div Human Reprod, 3900 Bandeirantes Ave, BR-14049900 Ribeirao Preto, SP - Brazil
[2] Univ Sao Paulo, Ribeirao Preto Med Sch, Dept Gynecol & Obstet, Lab Translat Data Sci, BR-14049900 Ribeirao Preto, SP - Brazil
[3] CNPq, Natl Inst Hormones & Womens Hlth Hormona, BR-90035003 Porto Alegre, RS - Brazil
[4] Univ Sao Paulo, Ctr Cell Therapy, BR-14051140 Ribeirao Preto, SP - Brazil
[5] Univ Sao Paulo, Reginal Blood Ctr, BR-14051140 Ribeirao Preto, SP - Brazil
Número total de Afiliações: 5
Tipo de documento: Artigo Científico
Fonte: REPRODUCTIVE SCIENCES; v. 29, n. 3, p. 734-742, MAR 2022.
Citações Web of Science: 0
Resumo

The key relationship between Sampson's theory and the presence of mesenchymal stem cells in the menstrual flow (MenSCs), as well as the changes in post-transcriptional regulatory processes as actors in the etiopathogenesis of endometriosis, are poorly understood. No study to date has investigated the imbalance of miRNAs in MenSCs related to the disease. Thus, through literature and in silico analyses, we selected four predicted miRNAs as regulators of EGR1, SNAI1, NR4A1, NR4A2, ID1, LAMC3, and FOSB involved in pathways of apoptosis, angiogenesis, response to steroid hormones, migration, differentiation, and cell proliferation. These genes are frequently overexpressed in the endometriosis condition in our group studies. They were the trigger for the miRNAs search. Therefore, a case-control study was conducted with MenSCs of women with and without endometriosis (ten samples per group). Crossing information obtained from the STRING, PubMed, miRPathDB, miRWalk, and DIANA TOOLS databases, we chose to explore the expression of miR-21-5p, miR-100-5p, miR-143-3p, and miR-200b-3p by RT-qPCR. We found an upregulation of the miR-200b-3p in endometriosis MenSCs (P = 0.0207), with a 7.93-fold change (ratio of geometric means) compared to control. Overexpression of miR-200b has been associated with increased cell proliferation, stemness, and accentuated mesenchymal-epithelial transition process in eutopic endometrium of endometriosis. We believe that dysregulated miR-200b-3p may establish primary changes in the MenSCs, thus favoring tissue implantation at the ectopic site. (AU)

Processo FAPESP: 13/22431-3 - Perfil diferencial de transcritos em células tronco mesenquimais obtidas do fluxo menstrual (MenMSCs) de mulheres com endometriose
Beneficiário:Juliana Meola Lovato
Modalidade de apoio: Auxílio à Pesquisa - Jovens Pesquisadores