Association of gene expression in ovarian granulosa cells with embryonic development potential among patients with polycystic ovary syndrome.
10.3760/cma.j.cn511374-20211109-00891
- Author:
Juan TENG
1
;
Ancong WANG
;
Xiangyu ZHAO
;
Meiju LIU
;
Yan WU
;
Lin LI
;
Wen LI
Author Information
1. Department of Genetic and Laboratory Medicine, Linyi People's Hospital, Linyi, Shandong 276000, China. 13869986938@126.com.
- Publication Type:Journal Article
- MeSH:
Female;
Humans;
Pregnancy;
Embryonic Development;
Gene Expression;
Gonadotropin-Releasing Hormone/antagonists & inhibitors*;
Granulosa Cells;
Polycystic Ovary Syndrome/genetics*
- From:
Chinese Journal of Medical Genetics
2022;39(12):1354-1359
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To assess the association of gene expression with development potential of early embryos derived from patients with polycystic ovary syndrome (PCOS).
METHODS:Three pairs of infertile patients with respectively matched age, body mass index, ovarian reserve and treatment with gonadotrophin-releasing hormone (GnRH) antagonists were selected. Patients with fewer embryos were assigned as the case group (n = 3), whilst the remainders were assigned as the control group (n = 3). Ovarian granulosa cells from patients were collected for the extraction of total RNA and subjected to RNA sequencing. The results were subjected to differential gene expression and functional enrichment analyses.
RESULTS:Compared with the control group, 76 genes were up-regulated and 110 genes were down-regulated in the case group. The level of estradiol (E2) was significantly higher in the control group on the trigger day with the injection of human chorionic gonadotrophin (HCG). Compared with the control group, the KRT7 gene was most significantly up-regulated, whilst the CCNYL2 gene was most significantly down-regulated in the case group. Gene ontology (GO) entries enrichment has found those associated with chromosome segregation, cell cycle regulation, and fatty acid metabolism to be significantly enriched. The genes participating in the regulation of cell assembly, differentiation, negative regulation of cell cycle, negative regulation of development, extracellular regulated protein kinases (ERK), ERK1 and ERK2 signaling pathways to be significantly down-regulated. KEGG enrichment analysis of cell signaling pathways revealed that steroid hormone biosynthesis-related genes were enriched.
CONCLUSION:Among patients treated with GnRH antagonists, the significant difference in the number of oocytes fertilized in vitro and the number of available embryos are associated with the difference in the expression of genes of ovarian granulosa cells.
