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Placental microRNA expression in pregnancies complicated by superimposed pre-eclampsia on chronic hypertension. / Vashukova, Elena S.; Glotov, Andrey S.; Fedotov, Pavel V.; Efimova, Olga A.; Pakin, Vladimir S.; Mozgovaya, Elena V.; Pendina, Anna A.; Tikhonov, Andrei V.; Koltsova, Alla S.; Baranov, Vladislav S.

в: Molecular Medicine Reports, Том 14, № 1, 01.07.2016, стр. 22-32.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Vashukova, ES, Glotov, AS, Fedotov, PV, Efimova, OA, Pakin, VS, Mozgovaya, EV, Pendina, AA, Tikhonov, AV, Koltsova, AS & Baranov, VS 2016, 'Placental microRNA expression in pregnancies complicated by superimposed pre-eclampsia on chronic hypertension', Molecular Medicine Reports, Том. 14, № 1, стр. 22-32. https://doi.org/10.3892/mmr.2016.5268

APA

Vashukova, E. S., Glotov, A. S., Fedotov, P. V., Efimova, O. A., Pakin, V. S., Mozgovaya, E. V., Pendina, A. A., Tikhonov, A. V., Koltsova, A. S., & Baranov, V. S. (2016). Placental microRNA expression in pregnancies complicated by superimposed pre-eclampsia on chronic hypertension. Molecular Medicine Reports, 14(1), 22-32. https://doi.org/10.3892/mmr.2016.5268

Vancouver

Vashukova ES, Glotov AS, Fedotov PV, Efimova OA, Pakin VS, Mozgovaya EV и пр. Placental microRNA expression in pregnancies complicated by superimposed pre-eclampsia on chronic hypertension. Molecular Medicine Reports. 2016 Июль 1;14(1):22-32. https://doi.org/10.3892/mmr.2016.5268

Author

Vashukova, Elena S. ; Glotov, Andrey S. ; Fedotov, Pavel V. ; Efimova, Olga A. ; Pakin, Vladimir S. ; Mozgovaya, Elena V. ; Pendina, Anna A. ; Tikhonov, Andrei V. ; Koltsova, Alla S. ; Baranov, Vladislav S. / Placental microRNA expression in pregnancies complicated by superimposed pre-eclampsia on chronic hypertension. в: Molecular Medicine Reports. 2016 ; Том 14, № 1. стр. 22-32.

BibTeX

@article{70064aba6e9841a5bf90d1eaffc80baf,
title = "Placental microRNA expression in pregnancies complicated by superimposed pre-eclampsia on chronic hypertension",
abstract = "Pre-eclampsia (PE) is a complication of pregnancy that affects 5-8% of women after 20 weeks of gestation. It is usually diagnosed based on the de novo onset of hypertension and proteinuria. Preexisting hypertension in women developing PE, also known as superimposed PE on chronic hypertension (SPE), leads to elevated risk of maternal and fetal mortality. PE is associated with an altered microRNA (miRNA) expression pattern in the placenta, suggesting that miRNA deregulation is involved in the pathogenesis of PE. Whether and how the miRNA expression pattern is changed in the SPE placenta remains unclear. The present study analyzed the placental miRNA expression profile in pregnancies complicated by SPE. miRNA expression profiles in SPE and normal placentas were investigated using an Ion Torrent sequencing system. Sequencing data were processed using a comprehensive analysis pipeline for deep miRNA sequencing (CAP-miRSeq). A total of 22 miRNAs were identified to be deregulated in placentas from patients with SPE. They included 16 miRNAs previously known to be associated with PE and 6 novel miRNAs. Among the 6 novel miRNAs, 4 were upregulated (miR-518a, miR-527, miR-518e and miR-4532) and 2 downregulated (miR-98 and miR-135b) in SPE placentas compared with controls. The present results suggest that SPE is associated with specific alterations in the placental miRNA expression pattern, which differ from alterations detected in PE placentas, and therefore, provide novel targets for further investigation of the molecular mechanisms underlying SPE pathogenesis.",
keywords = "Ion Torrent sequencing, MicroRNA, Placenta, Pre-eclampsia, Pregnancy complication, Superimposed pre-eclampsia on chronic hypertension",
author = "Vashukova, {Elena S.} and Glotov, {Andrey S.} and Fedotov, {Pavel V.} and Efimova, {Olga A.} and Pakin, {Vladimir S.} and Mozgovaya, {Elena V.} and Pendina, {Anna A.} and Tikhonov, {Andrei V.} and Koltsova, {Alla S.} and Baranov, {Vladislav S.}",
year = "2016",
month = jul,
day = "1",
doi = "10.3892/mmr.2016.5268",
language = "English",
volume = "14",
pages = "22--32",
journal = "Molecular Medicine Reports",
issn = "1791-2997",
publisher = "Spandidos Publications",
number = "1",

}

RIS

TY - JOUR

T1 - Placental microRNA expression in pregnancies complicated by superimposed pre-eclampsia on chronic hypertension

AU - Vashukova, Elena S.

AU - Glotov, Andrey S.

AU - Fedotov, Pavel V.

AU - Efimova, Olga A.

AU - Pakin, Vladimir S.

AU - Mozgovaya, Elena V.

AU - Pendina, Anna A.

AU - Tikhonov, Andrei V.

AU - Koltsova, Alla S.

AU - Baranov, Vladislav S.

PY - 2016/7/1

Y1 - 2016/7/1

N2 - Pre-eclampsia (PE) is a complication of pregnancy that affects 5-8% of women after 20 weeks of gestation. It is usually diagnosed based on the de novo onset of hypertension and proteinuria. Preexisting hypertension in women developing PE, also known as superimposed PE on chronic hypertension (SPE), leads to elevated risk of maternal and fetal mortality. PE is associated with an altered microRNA (miRNA) expression pattern in the placenta, suggesting that miRNA deregulation is involved in the pathogenesis of PE. Whether and how the miRNA expression pattern is changed in the SPE placenta remains unclear. The present study analyzed the placental miRNA expression profile in pregnancies complicated by SPE. miRNA expression profiles in SPE and normal placentas were investigated using an Ion Torrent sequencing system. Sequencing data were processed using a comprehensive analysis pipeline for deep miRNA sequencing (CAP-miRSeq). A total of 22 miRNAs were identified to be deregulated in placentas from patients with SPE. They included 16 miRNAs previously known to be associated with PE and 6 novel miRNAs. Among the 6 novel miRNAs, 4 were upregulated (miR-518a, miR-527, miR-518e and miR-4532) and 2 downregulated (miR-98 and miR-135b) in SPE placentas compared with controls. The present results suggest that SPE is associated with specific alterations in the placental miRNA expression pattern, which differ from alterations detected in PE placentas, and therefore, provide novel targets for further investigation of the molecular mechanisms underlying SPE pathogenesis.

AB - Pre-eclampsia (PE) is a complication of pregnancy that affects 5-8% of women after 20 weeks of gestation. It is usually diagnosed based on the de novo onset of hypertension and proteinuria. Preexisting hypertension in women developing PE, also known as superimposed PE on chronic hypertension (SPE), leads to elevated risk of maternal and fetal mortality. PE is associated with an altered microRNA (miRNA) expression pattern in the placenta, suggesting that miRNA deregulation is involved in the pathogenesis of PE. Whether and how the miRNA expression pattern is changed in the SPE placenta remains unclear. The present study analyzed the placental miRNA expression profile in pregnancies complicated by SPE. miRNA expression profiles in SPE and normal placentas were investigated using an Ion Torrent sequencing system. Sequencing data were processed using a comprehensive analysis pipeline for deep miRNA sequencing (CAP-miRSeq). A total of 22 miRNAs were identified to be deregulated in placentas from patients with SPE. They included 16 miRNAs previously known to be associated with PE and 6 novel miRNAs. Among the 6 novel miRNAs, 4 were upregulated (miR-518a, miR-527, miR-518e and miR-4532) and 2 downregulated (miR-98 and miR-135b) in SPE placentas compared with controls. The present results suggest that SPE is associated with specific alterations in the placental miRNA expression pattern, which differ from alterations detected in PE placentas, and therefore, provide novel targets for further investigation of the molecular mechanisms underlying SPE pathogenesis.

KW - Ion Torrent sequencing

KW - MicroRNA

KW - Placenta

KW - Pre-eclampsia

KW - Pregnancy complication

KW - Superimposed pre-eclampsia on chronic hypertension

UR - http://www.scopus.com/inward/record.url?scp=84973446483&partnerID=8YFLogxK

U2 - 10.3892/mmr.2016.5268

DO - 10.3892/mmr.2016.5268

M3 - Article

C2 - 27176897

AN - SCOPUS:84973446483

VL - 14

SP - 22

EP - 32

JO - Molecular Medicine Reports

JF - Molecular Medicine Reports

SN - 1791-2997

IS - 1

ER -

ID: 26202629