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Transcriptome analysis of eutopic endometrium in adenomyosis after GnRH agonist treatment.

Authors :
Tian J
Kang N
Wang J
Sun H
Yan G
Huang C
Mei J
Source :
Reproductive biology and endocrinology : RB&E [Reprod Biol Endocrinol] 2022 Jan 12; Vol. 20 (1), pp. 13. Date of Electronic Publication: 2022 Jan 12.
Publication Year :
2022

Abstract

Background: Adenomyosis is a chronic gynecological disease characterized by invasion of the uterine endometrium into the muscle layer. In assisted reproductive technology (ART), gonadotropin-releasing hormone agonist (GnRHa) is often used to improve pregnancy rates in patients with adenomyosis, but the underlying mechanisms are poorly understood.<br />Methods: Eutopic endometrial specimens were collected from patients with adenomyosis before and after GnRHa treatment in the midsecretory phase. RNA sequencing (RNA-Seq) of these specimens was performed for transcriptome analysis. The differentially expressed genes (DEGs) of interest were confirmed by real-time PCR and immunohistochemistry.<br />Results: A total of 132 DEGs were identified in the endometrium of patients with adenomyosis after GnRHa treatment compared with the control group. Bioinformatics analysis predicted that immune system-associated signal transduction changed significantly after GnRHa treatment. Chemokine (C-C motif) ligand 21 (CCL21) was found to be highly expressed in the eutopic endometrium after GnRHa treatment, which may be involved in the improvement of endometrial receptivity in adenomyosis.<br />Conclusion: This study suggests that molecular regulation related to immune system-associated signal transduction is an important mechanism of GnRHa treatment in adenomyosis. Immunoreactive CCL21 is thought to regulate inflammatory events and participate in endometrial receptivity in adenomyosis.<br /> (© 2022. The Author(s).)

Details

Language :
English
ISSN :
1477-7827
Volume :
20
Issue :
1
Database :
MEDLINE
Journal :
Reproductive biology and endocrinology : RB&E
Publication Type :
Academic Journal
Accession number :
35022045
Full Text :
https://doi.org/10.1186/s12958-021-00881-3