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CircSTAM inhibits migration and invasion of trophoblast cells by regulating miR-148a-5p/PTEN axis
BACKGROUND: The mechanisms underlying the pathogenesis of preeclampsia (PE) remains unclear. Exploring the molecular players in PE progression can provide insights into targeted therapy. METHODS: The expression levels of circSTAM in placental chorionic tissues of PE patients and normal pregnant wome...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9840740/ https://www.ncbi.nlm.nih.gov/pubmed/36471201 http://dx.doi.org/10.1007/s10815-022-02660-4 |
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author | Chen, Lingfeng Yan, Jinyu Zhang, Haiyan Xu, Jia Chen, Xiaopei |
author_facet | Chen, Lingfeng Yan, Jinyu Zhang, Haiyan Xu, Jia Chen, Xiaopei |
author_sort | Chen, Lingfeng |
collection | PubMed |
description | BACKGROUND: The mechanisms underlying the pathogenesis of preeclampsia (PE) remains unclear. Exploring the molecular players in PE progression can provide insights into targeted therapy. METHODS: The expression levels of circSTAM in placental chorionic tissues of PE patients and normal pregnant women were compared by RT-qPCR. CircSTAM was knocked down by small interfering RNA to investigate its role in migration, invasion and epithelial-mesenchymal transformation (EMT) of trophoblast HTR-8/SVneo cells. The downstream target of circSTAM was predicted using online bioinformatics resources, and their molecular interaction was examined by luciferase reporter assay. RESULTS: CircSTAM was upregulated in PE placenta tissues in comparison to normal placental tissues. CircSTAM knockdown significantly enhanced cellular invasion, migration, as well as EMT. Mir-148a-5p was identified as a target of circSTAM to regulate cell migration and invasion. Mir-148a-5p negatively regulated PTEN expression in trophoblast HTR-8 /SVneo cells. CONCLUSION: In summary, circSTAM upregulation in PE trophoblasts promoted the invasion, migration and EMT. CircSTAM may modulate trophoblast phenotype by impinging on mir-148a-5p/PTEN axis. These data provided novel insights into the pathogenesis of PE. |
format | Online Article Text |
id | pubmed-9840740 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-98407402023-01-16 CircSTAM inhibits migration and invasion of trophoblast cells by regulating miR-148a-5p/PTEN axis Chen, Lingfeng Yan, Jinyu Zhang, Haiyan Xu, Jia Chen, Xiaopei J Assist Reprod Genet Reproductive Physiology and Disease BACKGROUND: The mechanisms underlying the pathogenesis of preeclampsia (PE) remains unclear. Exploring the molecular players in PE progression can provide insights into targeted therapy. METHODS: The expression levels of circSTAM in placental chorionic tissues of PE patients and normal pregnant women were compared by RT-qPCR. CircSTAM was knocked down by small interfering RNA to investigate its role in migration, invasion and epithelial-mesenchymal transformation (EMT) of trophoblast HTR-8/SVneo cells. The downstream target of circSTAM was predicted using online bioinformatics resources, and their molecular interaction was examined by luciferase reporter assay. RESULTS: CircSTAM was upregulated in PE placenta tissues in comparison to normal placental tissues. CircSTAM knockdown significantly enhanced cellular invasion, migration, as well as EMT. Mir-148a-5p was identified as a target of circSTAM to regulate cell migration and invasion. Mir-148a-5p negatively regulated PTEN expression in trophoblast HTR-8 /SVneo cells. CONCLUSION: In summary, circSTAM upregulation in PE trophoblasts promoted the invasion, migration and EMT. CircSTAM may modulate trophoblast phenotype by impinging on mir-148a-5p/PTEN axis. These data provided novel insights into the pathogenesis of PE. Springer US 2022-12-06 2023-01 /pmc/articles/PMC9840740/ /pubmed/36471201 http://dx.doi.org/10.1007/s10815-022-02660-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Reproductive Physiology and Disease Chen, Lingfeng Yan, Jinyu Zhang, Haiyan Xu, Jia Chen, Xiaopei CircSTAM inhibits migration and invasion of trophoblast cells by regulating miR-148a-5p/PTEN axis |
title | CircSTAM inhibits migration and invasion of trophoblast cells by regulating miR-148a-5p/PTEN axis |
title_full | CircSTAM inhibits migration and invasion of trophoblast cells by regulating miR-148a-5p/PTEN axis |
title_fullStr | CircSTAM inhibits migration and invasion of trophoblast cells by regulating miR-148a-5p/PTEN axis |
title_full_unstemmed | CircSTAM inhibits migration and invasion of trophoblast cells by regulating miR-148a-5p/PTEN axis |
title_short | CircSTAM inhibits migration and invasion of trophoblast cells by regulating miR-148a-5p/PTEN axis |
title_sort | circstam inhibits migration and invasion of trophoblast cells by regulating mir-148a-5p/pten axis |
topic | Reproductive Physiology and Disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9840740/ https://www.ncbi.nlm.nih.gov/pubmed/36471201 http://dx.doi.org/10.1007/s10815-022-02660-4 |
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