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Differential expression of Hsa-miR-517a/b in placental tissue may contribute to the pathogenesis of preeclampsia
OBJECTIVE: Preeclampsia (PE) is a pregnancy hypertensive disorder that affects both maternal and fetal health. Many studies have investigated possible mechanisms in the pathogenesis of PE although the role of the placenta is undeniable. Evaluation of placental-specific microRNAs may provide addition...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Galenos Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8666996/ https://www.ncbi.nlm.nih.gov/pubmed/34866368 http://dx.doi.org/10.4274/jtgga.galenos.2021.2021.0062 |
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author | Amin-Beidokhti, Mona Sadeghi, Hossein Pirjani, Reihaneh Gachkar, Latif Gholami, Milad Mirfakhraie, Reza |
author_facet | Amin-Beidokhti, Mona Sadeghi, Hossein Pirjani, Reihaneh Gachkar, Latif Gholami, Milad Mirfakhraie, Reza |
author_sort | Amin-Beidokhti, Mona |
collection | PubMed |
description | OBJECTIVE: Preeclampsia (PE) is a pregnancy hypertensive disorder that affects both maternal and fetal health. Many studies have investigated possible mechanisms in the pathogenesis of PE although the role of the placenta is undeniable. Evaluation of placental-specific microRNAs may provide additional data about the pathogenic mechanism of PE. This study compared the expression levels of Hsa-miR-517a/b in placental tissues obtained from PE patients and healthy controls. MATERIAL AND METHODS: One hundred tissues were obtained from fetal and maternal sides of the placenta of PE patients and healthy controls. Expression analysis was performed using quantitative real-time polymerase chain reaction. RESULTS: Hsa-miR-517a/b level was significantly decreased in PE compared to controls (expression ratio: 0.40; p=0.007). Down-regulation of Hsa-miR-517a/b was also detected in fetal-side placental samples when compared to maternal-side in PE (expression ratio: 0.33; p=0.04). Furthermore, decreased expression of Hsa-miR-517a/b was detected in fetal-side tissue from PE cases compared to fetal-side samples from healthy pregnancies (expression ratio: 0.36; p=0.03). In maternal-side placental samples the expression level did not differ between PE and healthy pregnancies (p=0.1). CONCLUSION: These results demonstrate a differential expression of Hsa-miR-517a/b within placentas in pregnancies affected by PE and between placentas from PE and healthy pregnancies. Further studies are required to investigate a possible role for Hsa-miR-517a/b in the pathogenesis of PE. |
format | Online Article Text |
id | pubmed-8666996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Galenos Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-86669962021-12-16 Differential expression of Hsa-miR-517a/b in placental tissue may contribute to the pathogenesis of preeclampsia Amin-Beidokhti, Mona Sadeghi, Hossein Pirjani, Reihaneh Gachkar, Latif Gholami, Milad Mirfakhraie, Reza J Turk Ger Gynecol Assoc Original Investigation OBJECTIVE: Preeclampsia (PE) is a pregnancy hypertensive disorder that affects both maternal and fetal health. Many studies have investigated possible mechanisms in the pathogenesis of PE although the role of the placenta is undeniable. Evaluation of placental-specific microRNAs may provide additional data about the pathogenic mechanism of PE. This study compared the expression levels of Hsa-miR-517a/b in placental tissues obtained from PE patients and healthy controls. MATERIAL AND METHODS: One hundred tissues were obtained from fetal and maternal sides of the placenta of PE patients and healthy controls. Expression analysis was performed using quantitative real-time polymerase chain reaction. RESULTS: Hsa-miR-517a/b level was significantly decreased in PE compared to controls (expression ratio: 0.40; p=0.007). Down-regulation of Hsa-miR-517a/b was also detected in fetal-side placental samples when compared to maternal-side in PE (expression ratio: 0.33; p=0.04). Furthermore, decreased expression of Hsa-miR-517a/b was detected in fetal-side tissue from PE cases compared to fetal-side samples from healthy pregnancies (expression ratio: 0.36; p=0.03). In maternal-side placental samples the expression level did not differ between PE and healthy pregnancies (p=0.1). CONCLUSION: These results demonstrate a differential expression of Hsa-miR-517a/b within placentas in pregnancies affected by PE and between placentas from PE and healthy pregnancies. Further studies are required to investigate a possible role for Hsa-miR-517a/b in the pathogenesis of PE. Galenos Publishing 2021-12 2021-12-06 /pmc/articles/PMC8666996/ /pubmed/34866368 http://dx.doi.org/10.4274/jtgga.galenos.2021.2021.0062 Text en © Copyright 2021 by the Turkish-German Gynecological Education and Research Foundation https://creativecommons.org/licenses/by-nc-nd/4.0/Journal of the Turkish-German Gynecological Association published by Galenos Publishing House. |
spellingShingle | Original Investigation Amin-Beidokhti, Mona Sadeghi, Hossein Pirjani, Reihaneh Gachkar, Latif Gholami, Milad Mirfakhraie, Reza Differential expression of Hsa-miR-517a/b in placental tissue may contribute to the pathogenesis of preeclampsia |
title | Differential expression of Hsa-miR-517a/b in placental tissue may contribute to the pathogenesis of preeclampsia |
title_full | Differential expression of Hsa-miR-517a/b in placental tissue may contribute to the pathogenesis of preeclampsia |
title_fullStr | Differential expression of Hsa-miR-517a/b in placental tissue may contribute to the pathogenesis of preeclampsia |
title_full_unstemmed | Differential expression of Hsa-miR-517a/b in placental tissue may contribute to the pathogenesis of preeclampsia |
title_short | Differential expression of Hsa-miR-517a/b in placental tissue may contribute to the pathogenesis of preeclampsia |
title_sort | differential expression of hsa-mir-517a/b in placental tissue may contribute to the pathogenesis of preeclampsia |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8666996/ https://www.ncbi.nlm.nih.gov/pubmed/34866368 http://dx.doi.org/10.4274/jtgga.galenos.2021.2021.0062 |
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