LncRNA-mRNA regulatory network reveals key lncRNAs tightly associated with preterm labor and premature rupture of membranes
Guangqiong Yang, Wenjin Qi

TL;DR
This study identifies specific long non-coding RNAs linked to preterm labor and membrane rupture, offering new insights into their molecular causes.
Contribution
The study reveals novel lncRNA-mRNA regulatory interactions associated with preterm labor and premature rupture of membranes.
Findings
BBOX1-AS1, VIM-AS1, XLOC-031812, and AC106706.1 are lncRNAs potentially involved in PROM and PTB pathophysiology.
Co-expression analysis shows these lncRNAs regulate genes critical for pregnancy and placental development.
The lncRNA-mRNA axis is highlighted as a key factor in the onset and progression of PROM and PTB.
Abstract
Premature rupture of membranes (PROM) and preterm birth (PTB) are significant pregnancy complications, accounting for approximately one-third of PTB, often preceded by preterm PROM (PPROM). The underlying causes of PROM and PTB are multifaceted and not fully understood. Long non-coding RNAs (lncRNAs) have emerged as pivotal elements in the molecular landscape of PPROM. In our study, we analyzed fetal membrane samples from Term labor (TL), PROM, PTB, and PPROM groups using transcriptome sequencing to identify differentially expressed genes, including both lncRNAs and mRNAs. Our findings highlighted a subset of lncRNAs, BBOX1-AS1, VIM-AS1, XLOC-031812 and AC106706.1 as potentially influential in the pathophysiology of PROM and PTB. Co-expression analyses further revealed that the target genes regulated by these lncRNAs were significantly implicated in pregnancy progression and embryonic…
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Taxonomy
TopicsCancer-related molecular mechanisms research · Preterm Birth and Chorioamnionitis · Circular RNAs in diseases
