Research Paper Volume 16, Issue 10 pp 8585—8598
MiR-371-5p regulates trophoblast cell proliferation, migration, and invasion by directly targeting ZNF516
- 1 Electrocardiogram Room, Guangdong Women and Children Hospital, Guangzhou 511442, China
- 2 The Affiliated Guangdong Second Provincial General Hospital of Jinan University, Guangzhou 510317, China
- 3 University of South China’s Teaching Hospital, Guangdong Second Provincial General Hospital, Hengyang 421000, China
Received: September 18, 2023 Accepted: April 8, 2024 Published: May 17, 2024
https://doi.org/10.18632/aging.205826How to Cite
Copyright: © 2024 Chen et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Abstract
Despite its prevalence, preeclampsia (PE) remains unclear as to its etiology. Here, we aimed to investigate the mechanisms regulating differences in the gene expression of zinc-finger protein 516 (ZNF516) in the placenta. The expression of the placental ZNF516 gene and its association with critical clinical markers were verified, and a rigorous correlation analysis was conducted. With a dual-luciferase reporter gene assay, microRNA targeting the ZNF516 gene was predicted and confirmed. Finally, the molecular processes associated with ZNF516 were explored via microarray and bioinformatic analyses. In hypoxic conditions, miR-371-5p expression was reduced, resulting in ZNF516 expression being induced. Moreover, ZNF516 was shown to hinder trophoblast cell migration and invasion while enhancing trophoblast cell death in various in vitro cellular assays, such as cell counting kit-8, colony formation, wound healing, and Transwell assays. Our findings reveal a new regulatory network facilitated by ZNF516. ZNF516 overexpression inhibits trophoblast growth, movement, and penetration, potentially causing problems with placenta formation with the help of miR-371-5p suppression.