Identification and comparison of circular RNAs in preeclampsia

Zepeng Ping1, Ling Ai1, Huaxiang Shen1

  • 1Department of Obstetrics, Maternity and Child Health Care Affiliated Hospital, Jiaxing University, Jiaxing, China.

Peerj
|May 12, 2021
PubMed

Insights

Preeclampsia (PE) pathogenesis remains unclear. This study investigated circular RNA (circRNA) expression in PE patients, revealing differential expression and potential regulatory roles through competing endogenous RNA (ceRNA) networks, offering new insights into PE molecular mechanisms.

Area of Science:

  • Genomics
  • Molecular Biology
  • Obstetrics

Background:

  • Preeclampsia (PE) is a pregnancy-specific condition contributing to maternal and perinatal mortality.
  • The underlying pathogenesis of preeclampsia remains poorly understood.
  • Gestational hypertension diseases encompass preeclampsia, highlighting its clinical significance.

Purpose of the Study:

  • To investigate circular RNA (circRNA) expression patterns in preeclampsia (PE).
  • To explore the potential regulatory mechanisms of circRNAs in PE pathogenesis.
  • To construct competing endogenous RNA (ceRNA) networks to elucidate molecular roles of dysregulated circRNAs.

Main Methods:

  • Whole RNA sequencing was employed to analyze circRNA expression profiles.
  • Gene Ontology and KEGG pathway analyses were performed on differentially expressed circRNAs.
  • circRNA-microRNA (miRNA) and miRNA-mRNA interactions were analyzed to construct ceRNA networks.

Main Results:

  • 151 differentially expressed circRNAs were identified (121 upregulated, 30 downregulated).
  • Enrichment analysis indicated significant biological process and pathway alterations in PE patients.
  • Two ceRNA networks were constructed, revealing complex regulatory interactions involving circRNAs, miRNAs, and mRNAs.
  • circRNA_13301 was identified as a key upregulated circRNA targeted by multiple miRNAs.

Conclusions:

  • CircRNA expression patterns are altered in preeclampsia, suggesting their involvement in disease pathogenesis.
  • ceRNA networks provide insights into the molecular roles of dysregulated circRNAs in PE.
  • Further research into circRNA regulatory networks may uncover novel therapeutic targets for preeclampsia.
Abstract

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