Evidence map›Paper›PMID 39134922›Full record

ArticleReproductive sciences (Thousand Oaks, Calif.)2024

hsa_circ_0088196 Predicts Adverse Pregnancy Outcomes in Preeclampsia Patients and Contributes to Endothelial Cell Injury Via Modulating the miR-145-5p/FLT1 Axis.

Yuelai Yang, Lei Jiang, Ruijing Chang, Jing Liu, Hong Xin, Wanli Ji

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Article in Reproductive sciences (Thousand Oaks, Calif.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Yuelai YangDepartment of Anesthesiology, Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine, Shanghai, 200011, China.
Lei JiangDepartment of Obstetrics, The Second Hospital of Hebei Medical University, Shijiazhuang, 050004, China.
Ruijing ChangDepartment of Obstetrics, The Second Hospital of Hebei Medical University, Shijiazhuang, 050004, China.
Jing LiuDepartment of Obstetrics, Shijiazhuang Maternity & Child Healthcare Hospital, Shijiazhuang, 050006, China.
Hong XinDepartment of Obstetrics, The Second Hospital of Hebei Medical University, Shijiazhuang, 050004, China.
Wanli JiDepartment of Gynaecology and Obstetrics, Nanjing Luhe People's Hospital, No. 28, Yan'an Road, Luhe District, Nanjing, 211599, China. Jiwl1981@163.com.

Funding

Leader Incubation Program of Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine JYHRC22-L04Shanghai Hospital Development Center 2022 Municipal Hospital Diagnosis and Treatment Technology Promotion and Optimization Management Project-Technology Standardization Management and Promotion Project SHDC22022226
6 · The paper itself

Abstract

Preeclampsia (PE) is a specific hypertension-related disease in pregnancies, causing adverse pregnancy outcomes. Endothelial cell dysfunction is a major etiology of PE, of which the regulation could affect disease progression. This study focused on hsa_circ_0088196, evaluating its clinical significance in PE and its effect on endothelial cell injury, aiming to identify a novel biomarker for PE and complete its regulating mechanism in disease development. The study enrolled 165 normal pregnancies and 165 pregnancies with gestational hypertension. The significance of hsa_circ_0088196 in discriminating gestational hypertension, predicting PE, and predicting adverse pregnancy outcomes was evaluated based on its serum expression. The effect and mechanism of hsa_circ_0088196 in HUVEC injury were assessed by CCK8, Transwell, ELISA, and western blotting. Significant downregulation of hsa_circ_0088196 could distinguish gestational hypertension pregnancies and predict the risk of PE. Gestational hypertension pregnancies developed PE showed a lower serum hsa_circ_0088196 level, which also discriminated PE patients, predicted severe conditions and adverse pregnancy outcomes. Overexpressing hsa_circ_0088196 alleviated the enhanced proliferation, migration, inflammation, and angiogenesis by hypoxia/reoxygenation (H/R), which was reversed by miR-145-5p. Silencing miR-145-5p showed similar effects on H/R-induced endothelial cell injury, which was reversed by FLT1. Moreover, FLT1 was positively regulated by hsa_circ_0088196, indicating its involvement in the regulation of HUVEC injury by hsa_circ_0088196. Reduced serum hsa_circ_0088196 served as a biomarker for the diagnosis of gestational hypertension, risk evaluation of PE, and the prediction of adverse pregnancy outcomes. hsa_circ_0088196 suppressed endothelial cell injury induced by H/R through modulating the miR-145-5p/FLT1 axis.

Indexed as

MicroRNAsPre-EclampsiaPregnancy OutcomeRNA, CircularVascular Endothelial Growth Factor Receptor-1AdultBiomarkersFemaleHumansHuman Umbilical Vein Endothelial CellsPregnancyBiomarkersFLT1 protein, humanMicroRNAsMIRN145 microRNA, humanRNA, CircularVascular Endothelial Growth Factor Receptor-1Adverse pregnancy outcomesCeRNA regulationEndothelial injuryGestational hypertension

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.