Analysis of the Differential Expression of Genes Involved in Pathways of Cell Proliferation, Differentiation and Inflammatory Responses in the Eutopic Endometrium of Patients with and Without Endometriosis

An observational cross-sectional study was conducted in a university hospital to evaluate eutopic endometria from women who underwent a laparoscopy, comprising 20 patients with endometriosis and 25 without the disease (control group). The differential gene expression was analyzed between the groups by RT-qPCR for the genes FOS, FOSB, JUNB, and EGR1, which are involved in common pathways regulating cell differentiation and proliferation and the early response to inflammatory insults. In the endometriosis group, the mean patient’s age was 36.4 years, and 34.4 years in the control group. The groups were homogeneous with respect to clinical variables, except for the parity, which showed a higher frequency of nulliparous women among endometriosis patients. Most of the included patients in both groups were on hormonal medications. There was no difference between the groups in the expression of EGR1 (p = 0.9231), FOS (p = 0.1261), or FOSB (p = 0.8249). Concerning JUNB, we observed a higher expression in the control group in comparison with endometriosis patients (p = 0.0417). These results may reflect the paradoxical role of JUNB in modulating proliferation and apoptosis and highlight possible biological variability among different populations. Finally, analyzing only the eutopic endometrium may not shed light on the complexity of the endometriosis pathophysiology, since the endometrium undergoes critical modifications when present outside the uterus and in the context of already established disease. Future studies should aim to better understand the peritoneal microenvironment, prioritizing broader evaluations of post-transcriptional factors.

Authors

Institutions

Publication Details

Journal
Current Issues in Molecular Biology
Published
2026-11-11
DOI
https://doi.org/10.3390/cimb48111193
Primary Topic
Endometriosis Research and Treatment
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
NOV
article

Analysis of the Differential Expression of Genes Involved in Pathways of Cell Proliferation, Differentiation and Inflammatory Responses in the Eutopic Endometrium of Patients with and Without Endometriosis

Júlio Dos Santos Silva, Júlia Kefalás Troncon, Carla de Azevedo Piccinato, Juliana Meola et al.
Current Issues in Molecular Biology
Endometriosis Research and Treatment
article

Analysis of the Differential Expression of Genes Involved in Pathways of Cell Proliferation, Differentiation and Inflammatory Responses in the Eutopic Endometrium of Patients with and Without Endometriosis

Júlio Dos Santos Silva, Júlia Kefalás Troncon, Carla de Azevedo Piccinato, Juliana Meola, Omero Benedicto Poli‐Neto, Isabela Nardo
article en

Abstract

An observational cross-sectional study was conducted in a university hospital to evaluate eutopic endometria from women who underwent a laparoscopy, comprising 20 patients with endometriosis and 25 without the disease (control group). The differential gene expression was analyzed between the groups by RT-qPCR for the genes FOS, FOSB, JUNB, and EGR1, which are involved in common pathways regulating cell differentiation and proliferation and the early response to inflammatory insults. In the endometriosis group, the mean patient’s age was 36.4 years, and 34.4 years in the control group. The groups were homogeneous with respect to clinical variables, except for the parity, which showed a higher frequency of nulliparous women among endometriosis patients. Most of the included patients in both groups were on hormonal medications. There was no difference between the groups in the expression of EGR1 (p = 0.9231), FOS (p = 0.1261), or FOSB (p = 0.8249). Concerning JUNB, we observed a higher expression in the control group in comparison with endometriosis patients (p = 0.0417). These results may reflect the paradoxical role of JUNB in modulating proliferation and apoptosis and highlight possible biological variability among different populations. Finally, analyzing only the eutopic endometrium may not shed light on the complexity of the endometriosis pathophysiology, since the endometrium undergoes critical modifications when present outside the uterus and in the context of already established disease. Future studies should aim to better understand the peritoneal microenvironment, prioritizing broader evaluations of post-transcriptional factors.

Current Issues in Molecular BiologyVol. 48(11)
Universidade de São Paulo (BR)
Endometriosis Research and Treatment
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Laika access coming soon