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Expression of ezrin protein and phosphorylated ezrin in pelvic endometriotic lesions

OBJECTIVE: To evaluate the expression of Ezrin and Phosphorylated Ezrin (Phospho-Ezrin) in endometriosis lesions and its relation to the menstrual cycle phase, stage of endometriosis, histological classification, and clinical symptoms. MATERIAL AND METHODS: The authors conducted a retrospective stud...

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Autores principales: Peloggia, Alessandra, Andres, Marina Paula, Abrão, Mauricio Simões
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hospital das Clinicas da Faculdade de Medicina da Universidade de Sao Paulo 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9260236/
https://www.ncbi.nlm.nih.gov/pubmed/35793608
http://dx.doi.org/10.1016/j.clinsp.2022.100074
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author Peloggia, Alessandra
Andres, Marina Paula
Abrão, Mauricio Simões
author_facet Peloggia, Alessandra
Andres, Marina Paula
Abrão, Mauricio Simões
author_sort Peloggia, Alessandra
collection PubMed
description OBJECTIVE: To evaluate the expression of Ezrin and Phosphorylated Ezrin (Phospho-Ezrin) in endometriosis lesions and its relation to the menstrual cycle phase, stage of endometriosis, histological classification, and clinical symptoms. MATERIAL AND METHODS: The authors conducted a retrospective study, with endometriotic lesions collected from women with endometriosis (n = 57) who underwent laparoscopy from 2017 to 2018. The expression of Ezrin and Phosphorylated Ezrin proteins was analyzed by immunohistochemistry. RESULTS: All the endometriotic lesions contained immunostaining for Ezrin in the glands. Phosphorylated Ezrin was expressed in the stroma of all endometriotic lesions. There was no difference in the Ezrin and Phosphorylated Ezrin's expression in the retrocervical, ovarian, superficial, and intestinal lesions in the same patient. Dysmenorrhea, dyspareunia, acyclic pain, infertility, and dysuria were similar in the three groups of Ezrin staining. There was an inversely proportional relationship between severe dyschezia and Ezrin's intensity, being 66.7% of Ezrin 1 (weak intensity), 36.7 Ezrin 2 (moderate intensity), and 10.0% of Ezrin 3 (p = 0.013). Regarding Phospho-Ezrin there wasn't a significant difference between all the analyzed variables. Histological classification and menstrual cycle phase had also no significant difference between Ezrin and Phospho-Ezrin immunostaining. CONCLUSION: Ezrin protein and Phospho-Ezrin can be considered important markers to elucidate the mechanisms related to migration and attachment of endometriotic lesions. It is still unclear if Ezrin and Phospho-Ezrin are a cause or consequence of endometriosis. Further studies comparing different types of lesions and eutopic endometrium are necessary to elucidate the role of these proteins in the pathogenesis of endometriosis.
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spelling pubmed-92602362022-07-08 Expression of ezrin protein and phosphorylated ezrin in pelvic endometriotic lesions Peloggia, Alessandra Andres, Marina Paula Abrão, Mauricio Simões Clinics (Sao Paulo) Original Articles OBJECTIVE: To evaluate the expression of Ezrin and Phosphorylated Ezrin (Phospho-Ezrin) in endometriosis lesions and its relation to the menstrual cycle phase, stage of endometriosis, histological classification, and clinical symptoms. MATERIAL AND METHODS: The authors conducted a retrospective study, with endometriotic lesions collected from women with endometriosis (n = 57) who underwent laparoscopy from 2017 to 2018. The expression of Ezrin and Phosphorylated Ezrin proteins was analyzed by immunohistochemistry. RESULTS: All the endometriotic lesions contained immunostaining for Ezrin in the glands. Phosphorylated Ezrin was expressed in the stroma of all endometriotic lesions. There was no difference in the Ezrin and Phosphorylated Ezrin's expression in the retrocervical, ovarian, superficial, and intestinal lesions in the same patient. Dysmenorrhea, dyspareunia, acyclic pain, infertility, and dysuria were similar in the three groups of Ezrin staining. There was an inversely proportional relationship between severe dyschezia and Ezrin's intensity, being 66.7% of Ezrin 1 (weak intensity), 36.7 Ezrin 2 (moderate intensity), and 10.0% of Ezrin 3 (p = 0.013). Regarding Phospho-Ezrin there wasn't a significant difference between all the analyzed variables. Histological classification and menstrual cycle phase had also no significant difference between Ezrin and Phospho-Ezrin immunostaining. CONCLUSION: Ezrin protein and Phospho-Ezrin can be considered important markers to elucidate the mechanisms related to migration and attachment of endometriotic lesions. It is still unclear if Ezrin and Phospho-Ezrin are a cause or consequence of endometriosis. Further studies comparing different types of lesions and eutopic endometrium are necessary to elucidate the role of these proteins in the pathogenesis of endometriosis. Hospital das Clinicas da Faculdade de Medicina da Universidade de Sao Paulo 2022-07-03 /pmc/articles/PMC9260236/ /pubmed/35793608 http://dx.doi.org/10.1016/j.clinsp.2022.100074 Text en © 2022 HCFMUSP. Published by Elsevier España, S.L.U. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Articles
Peloggia, Alessandra
Andres, Marina Paula
Abrão, Mauricio Simões
Expression of ezrin protein and phosphorylated ezrin in pelvic endometriotic lesions
title Expression of ezrin protein and phosphorylated ezrin in pelvic endometriotic lesions
title_full Expression of ezrin protein and phosphorylated ezrin in pelvic endometriotic lesions
title_fullStr Expression of ezrin protein and phosphorylated ezrin in pelvic endometriotic lesions
title_full_unstemmed Expression of ezrin protein and phosphorylated ezrin in pelvic endometriotic lesions
title_short Expression of ezrin protein and phosphorylated ezrin in pelvic endometriotic lesions
title_sort expression of ezrin protein and phosphorylated ezrin in pelvic endometriotic lesions
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9260236/
https://www.ncbi.nlm.nih.gov/pubmed/35793608
http://dx.doi.org/10.1016/j.clinsp.2022.100074
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