TY - JOUR
T1 - Pre-eclampsia predictive ability of maternal miR-125b
T2 - a clinical and experimental study
AU - Licini, Caterina
AU - Avellini, Chiara
AU - Picchiassi, Elena
AU - Mensà, Emanuela
AU - Fantone, Sonia
AU - Ramini, Deborah
AU - Tersigni, Chiara
AU - Tossetta, Giovanni
AU - Castellucci, Clara
AU - Tarquini, Federica
AU - Coata, Giuliana
AU - Giardina, Irene
AU - Ciavattini, Andrea
AU - Scambia, Giovanni
AU - Di Renzo, Gian Carlo
AU - Di Simone, Nicoletta
AU - Gesuita, Rosaria
AU - Giannubilo, Stefano R.
AU - Olivieri, Fabiola
AU - Marzioni, Daniela
N1 - Funding Information:
We are grateful to Dr Charles Graham (Queen's University, Kingston, ON, Canada) for his kind gift of HTR-8/SV-neo cells, to Prof Luca Tiano (Universit? Politecnica delle Marche, Ancona, Italy), to Prof Berthold Huppertz (Medical University of Graz, Graz, Austria), and to Prof Saverio Alberti and Dr Emanuela Guerra (Laboratory of Cancer Pathology, CeSI-MeT, University 'G. d'Annunzio', Chieti, Italy) for valuable advice, and to Dr. Martina Senzacqua for her technical assistance with the confocal microscope. All authors have read the journal's authorship agreement and policy on disclosure of potential conflicts of interest and they declare no conflict of interest. They have read, reviewed and approved the manuscript. Financial support: This work was supported partly by Italian Ministry of University and Research (PRIN 2010) to GCDR, SRG and by a Scientific Research Grant from Universit? Politecnica delle Marche (RSA 2016-2017-2018) to SRG, FO, DM.
Funding Information:
We are grateful to Dr Charles Graham (Queen's University, Kingston, ON, Canada) for his kind gift of HTR-8/SV-neo cells, to Prof Luca Tiano (Università Politecnica delle Marche, Ancona, Italy), to Prof Berthold Huppertz (Medical University of Graz, Graz, Austria), and to Prof Saverio Alberti and Dr Emanuela Guerra (Laboratory of Cancer Pathology, CeSI-MeT, University 'G. d'Annunzio', Chieti, Italy) for valuable advice, and to Dr. Martina Senzacqua for her technical assistance with the confocal microscope. All authors have read the journal's authorship agreement and policy on disclosure of potential conflicts of interest and they declare no conflict of interest. They have read, reviewed and approved the manuscript. Financial support : This work was supported partly by Italian Ministry of University and Research (PRIN 2010) to GCDR, SRG and by a Scientific Research Grant from Università Politecnica delle Marche (RSA 2016-2017-2018) to SRG, FO, DM.
Publisher Copyright:
© 2020 Elsevier Inc.
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/2
Y1 - 2021/2
N2 - Pre-eclampsia (PE) is a systemic maternal syndrome affecting 2-8% of pregnancies worldwide and involving poor placental perfusion and impaired blood supply to the foetus. It manifests after the 20th week of pregnancy as new-onset hypertension and substantial proteinuria and is responsible for severe maternal and newborn morbidity and mortality. Identifying biomarkers that predict PE onset prior to its establishment would critically help treatment and attenuate outcome severity. MicroRNAs are ubiquitous gene expression modulators found in blood and tissues. Trophoblast cell surface antigen (Trop)-2 promotes cell growth and is involved in several cancers. We assessed the PE predictive ability of maternal miR-125b in the first trimester of pregnancy by measuring its plasma levels in women with normal pregnancies and with pregnancies complicated by PE on the 12th week of gestation. To gain insight into PE pathogenesis we investigated whether Trop-2 is targeted by miR-125b in placental tissue. Data analysis demonstrated a significant association between plasma miR-125b levels and PE, which together with maternal body mass index before pregnancy provided a predictive model with an area under the curve of 0.85 (95% confidence interval, 0.70-1.00). We also found that Trop-2 is a target of miR-125b in placental cells; its localization in the basal part of the syncytiotrophoblast plasma membrane suggests a role for it in the early onset of PE. Altogether, maternal miR-125b proved a promising early biomarker of PE, suggesting that it may be involved in placental development through its action on Trop-2 well before the clinical manifestations of PE.
AB - Pre-eclampsia (PE) is a systemic maternal syndrome affecting 2-8% of pregnancies worldwide and involving poor placental perfusion and impaired blood supply to the foetus. It manifests after the 20th week of pregnancy as new-onset hypertension and substantial proteinuria and is responsible for severe maternal and newborn morbidity and mortality. Identifying biomarkers that predict PE onset prior to its establishment would critically help treatment and attenuate outcome severity. MicroRNAs are ubiquitous gene expression modulators found in blood and tissues. Trophoblast cell surface antigen (Trop)-2 promotes cell growth and is involved in several cancers. We assessed the PE predictive ability of maternal miR-125b in the first trimester of pregnancy by measuring its plasma levels in women with normal pregnancies and with pregnancies complicated by PE on the 12th week of gestation. To gain insight into PE pathogenesis we investigated whether Trop-2 is targeted by miR-125b in placental tissue. Data analysis demonstrated a significant association between plasma miR-125b levels and PE, which together with maternal body mass index before pregnancy provided a predictive model with an area under the curve of 0.85 (95% confidence interval, 0.70-1.00). We also found that Trop-2 is a target of miR-125b in placental cells; its localization in the basal part of the syncytiotrophoblast plasma membrane suggests a role for it in the early onset of PE. Altogether, maternal miR-125b proved a promising early biomarker of PE, suggesting that it may be involved in placental development through its action on Trop-2 well before the clinical manifestations of PE.
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U2 - 10.1016/j.trsl.2020.07.011
DO - 10.1016/j.trsl.2020.07.011
M3 - Article
C2 - 32726711
AN - SCOPUS:85089745068
SN - 1931-5244
VL - 228
SP - 13
EP - 27
JO - Translational Research
JF - Translational Research
ER -