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Evaluation of Rap1GAP and EPAC1 Gene Expression in Endometriosis Disease

BACKGROUND: Endometriosis is a female reproductive system disease in which the endometrial tissue is found in other women's organs. Various factors are effective in the development of endometriosis, and because of the interaction of genetics and environmental factors, this disease is a multi-fa...

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Autores principales: Dehghanian, Mehran, Yarahmadi, Ghafour, Sandoghsaz, Reyhaneh Sadat, Khodadadian, Ali, Shamsi, Farimah, Vahidi Mehrjardi, Mohammad Yahya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241619/
https://www.ncbi.nlm.nih.gov/pubmed/37288024
http://dx.doi.org/10.4103/abr.abr_86_22
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author Dehghanian, Mehran
Yarahmadi, Ghafour
Sandoghsaz, Reyhaneh Sadat
Khodadadian, Ali
Shamsi, Farimah
Vahidi Mehrjardi, Mohammad Yahya
author_facet Dehghanian, Mehran
Yarahmadi, Ghafour
Sandoghsaz, Reyhaneh Sadat
Khodadadian, Ali
Shamsi, Farimah
Vahidi Mehrjardi, Mohammad Yahya
author_sort Dehghanian, Mehran
collection PubMed
description BACKGROUND: Endometriosis is a female reproductive system disease in which the endometrial tissue is found in other women's organs. Various factors are effective in the development of endometriosis, and because of the interaction of genetics and environmental factors, this disease is a multi-factorial disease. MAPK/ERK and PI3K/Akt/mTOR pathways are activated by growth factors and steroid hormones and are known as two important pathways involved in the processes of growth, proliferation, and survival of endometriosis cells. Raps, monomeric GTPase of the Ras family, are able to activate these pathways independent of Ras. The goal of our study was to evaluate the expression level of Rap1GAP and EPAC1 genes as two important RapGAPs (GTPase-activating proteins) and RapGEFs (guanine nucleotide exchange factors), respectively, in endometriosis tissues and normal endometrium tissues. MATERIALS AND METHODS: In this study, 15 samples of women without signs of endometriosis were taken as control samples. Fifteen ectopic and 15 eutopic samples were taken from women with endometriosis using laparoscopic surgery. The expression of EPAC1 and Rap1GAP genes was investigated by the real-time polymerase chain reaction technique, and the results were analyzed by one-way ANOVA test. RESULTS: EPAC1 upregulated significantly in ectopic tissues compared to eutopic and control tissues. Rap1GAP expression was lower in ectopic tissues compared to control and eutopic tissues. CONCLUSIONS: Based on these results, it may be concluded that changes in the expression of the Rap1GAP and Epca1 genes may play a role in the pathways involved in the pathogenesis, displacement, and migration of endometriosis cells.
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spelling pubmed-102416192023-06-07 Evaluation of Rap1GAP and EPAC1 Gene Expression in Endometriosis Disease Dehghanian, Mehran Yarahmadi, Ghafour Sandoghsaz, Reyhaneh Sadat Khodadadian, Ali Shamsi, Farimah Vahidi Mehrjardi, Mohammad Yahya Adv Biomed Res Original Article BACKGROUND: Endometriosis is a female reproductive system disease in which the endometrial tissue is found in other women's organs. Various factors are effective in the development of endometriosis, and because of the interaction of genetics and environmental factors, this disease is a multi-factorial disease. MAPK/ERK and PI3K/Akt/mTOR pathways are activated by growth factors and steroid hormones and are known as two important pathways involved in the processes of growth, proliferation, and survival of endometriosis cells. Raps, monomeric GTPase of the Ras family, are able to activate these pathways independent of Ras. The goal of our study was to evaluate the expression level of Rap1GAP and EPAC1 genes as two important RapGAPs (GTPase-activating proteins) and RapGEFs (guanine nucleotide exchange factors), respectively, in endometriosis tissues and normal endometrium tissues. MATERIALS AND METHODS: In this study, 15 samples of women without signs of endometriosis were taken as control samples. Fifteen ectopic and 15 eutopic samples were taken from women with endometriosis using laparoscopic surgery. The expression of EPAC1 and Rap1GAP genes was investigated by the real-time polymerase chain reaction technique, and the results were analyzed by one-way ANOVA test. RESULTS: EPAC1 upregulated significantly in ectopic tissues compared to eutopic and control tissues. Rap1GAP expression was lower in ectopic tissues compared to control and eutopic tissues. CONCLUSIONS: Based on these results, it may be concluded that changes in the expression of the Rap1GAP and Epca1 genes may play a role in the pathways involved in the pathogenesis, displacement, and migration of endometriosis cells. Wolters Kluwer - Medknow 2023-04-27 /pmc/articles/PMC10241619/ /pubmed/37288024 http://dx.doi.org/10.4103/abr.abr_86_22 Text en Copyright: © 2023 Advanced Biomedical Research https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Dehghanian, Mehran
Yarahmadi, Ghafour
Sandoghsaz, Reyhaneh Sadat
Khodadadian, Ali
Shamsi, Farimah
Vahidi Mehrjardi, Mohammad Yahya
Evaluation of Rap1GAP and EPAC1 Gene Expression in Endometriosis Disease
title Evaluation of Rap1GAP and EPAC1 Gene Expression in Endometriosis Disease
title_full Evaluation of Rap1GAP and EPAC1 Gene Expression in Endometriosis Disease
title_fullStr Evaluation of Rap1GAP and EPAC1 Gene Expression in Endometriosis Disease
title_full_unstemmed Evaluation of Rap1GAP and EPAC1 Gene Expression in Endometriosis Disease
title_short Evaluation of Rap1GAP and EPAC1 Gene Expression in Endometriosis Disease
title_sort evaluation of rap1gap and epac1 gene expression in endometriosis disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241619/
https://www.ncbi.nlm.nih.gov/pubmed/37288024
http://dx.doi.org/10.4103/abr.abr_86_22
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