Identification of shared gene signatures and biological mechanisms between preeclampsia and polycystic ovary syndrome

被引:2
作者
Xiong, Yaoxi [1 ,2 ]
Chen, Chao [1 ,2 ]
He, Chengrong [1 ,2 ]
Yang, Xingyu [1 ,2 ]
Cheng, Weiwei [1 ]
机构
[1] Shanghai Jiao Tong Univ, Int Peace Matern & Child Hlth Hosp, Sch Med, Shanghai 200030, Peoples R China
[2] Shanghai Key Lab Embryo Original Dis, Shanghai 200030, Peoples R China
基金
中国国家自然科学基金;
关键词
Preeclampsia; Polycystic ovary syndrome; WGCNA; Bioinformatics; DDX58; I-LIKE RECEPTORS; RIG-I; PATHWAY; DIAGNOSIS; ETIOLOGY; INSIGHTS; PACKAGE;
D O I
10.1016/j.heliyon.2024.e29225
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Preeclampsia (PE) is one of the most common complications of pregnancy and polycystic ovary syndrome (PCOS) is a prevalent metabolic and endocrinopathy disorder in women of reproductive age. Identifying the shared genetic signatures and molecular mechanisms between PCOS and PE was the objective of this study. The intersections of WGCNA module genes, PPI module genes, and PPI hub genes revealed that 8 immunity-related genes might be shared causative genes of PE and PCOS. Further, qRT-PCR results showed that TSIX/miR-223-3p/DDX58 might play a crucial role in immune dysregulation in PE and PCOS and Spearman rank correlation analysis results illustrated the potential of DDX58 as a novel diagnostic and therapeutic target for PE and PCOS. Our study demonstrated a common disease pathway model TSIX/miR-223-3p/DDX58, illustrating that immune dysregulation may be a possible mechanism of PE and PCOS, and revealed that DDX58 might be a novel predictive target for PE and PCOS.
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页数:13
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