MicroRNAs: New Players in the Pathobiology of Preeclampsia

被引:87
作者
Bounds, Kelsey R. [1 ]
Chiasson, Valorie L. [1 ]
Pan, Lu J. [1 ]
Gupta, Sudhiranjan [2 ]
Chatterjee, Piyali [1 ]
机构
[1] Texas A&M Hlth Sci Ctr, Baylor Scott & White Hlth, Dept Internal Med, Temple, TX 76508 USA
[2] Texas A&M Hlth Sci Ctr, Baylor Scott & White Hlth, Dept Med Physiol, Temple, TX USA
关键词
pregnancy; microRNAs; preeclampsia; angiogenesis; inflammation; CELL-PROLIFERATION; EXPRESSION PROFILE; TROPHOBLAST CELLS; HUMAN PLACENTAS; GROWTH-FACTOR; CYR61; CCN1; MIR-210; PREGNANCIES; BIOGENESIS; MECHANISMS;
D O I
10.3389/fcvm.2017.00060
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Our understanding of how microRNAs (miRNAs) regulate gene networks and affect different molecular pathways leading to various human pathologies has significantly improved over the years. In contrary, the role of miRNAs in pregnancy-related hypertensive disorders such as preeclampsia (PE) is only beginning to emerge. Recent papers highlight that adverse pregnancy outcomes are associated with aberrant expression of several miRNAs. Presently, efforts are underway to determine the biologic function of these placental miRNAs which can shed light on their contribution to these pregnancy-related disease conditions. The discovery that miRNAs are stable in circulation coupled with the fact that the placenta is capable of releasing them to the circulation in exosomes generates a lot of enthusiasm to use them as biomarkers. In this review, we will summarize the recent findings of our understanding of miRNA regulation in relation to PE, a hypertensive disorder of pregnancy. Particular emphasis will be given to the role of key miRNA molecules such as miR-210 and miR-155 that are known to be consistently dysregulated in women with PE.
引用
收藏
页数:9
相关论文
共 80 条
[1]   MicroRNAs: new regulators of immune cell development and function [J].
Baltimore, David ;
Boldin, Mark P. ;
O'Connell, Ryan M. ;
Rao, Dinesh S. ;
Taganov, Konstantin D. .
NATURE IMMUNOLOGY, 2008, 9 (08) :839-845
[2]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[3]   Identification of hundreds of conserved and nonconserved human microRNAs [J].
Bentwich, I ;
Avniel, A ;
Karov, Y ;
Aharonov, R ;
Gilad, S ;
Barad, O ;
Barzilai, A ;
Einat, P ;
Einav, U ;
Meiri, E ;
Sharon, E ;
Spector, Y ;
Bentwich, Z .
NATURE GENETICS, 2005, 37 (07) :766-770
[4]   Mammalian mirtron genes [J].
Berezikov, Eugene ;
Chung, Wei-Jen ;
Willis, Jason ;
Cuppen, Edwin ;
Lai, Eric C. .
MOLECULAR CELL, 2007, 28 (02) :328-336
[5]   Dicer is essential for mouse development [J].
Bernstein, E ;
Kim, SY ;
Carmell, MA ;
Murchison, EP ;
Alcorn, H ;
Li, MZ ;
Mills, AA ;
Elledge, SJ ;
Anderson, KV ;
Hannon, GJ .
NATURE GENETICS, 2003, 35 (03) :215-217
[6]   First microRNA mimic enters clinic [J].
Bouchie, Aaron .
NATURE BIOTECHNOLOGY, 2013, 31 (07) :577-577
[7]  
Bounds Kelsey R, 2015, Front Cardiovasc Med, V2, P20, DOI 10.3389/fcvm.2015.00020
[8]   Spiral Artery Remodeling in Preeclampsia Revisited [J].
Burke, Suzanne D. ;
Karumanchi, S. Ananth .
HYPERTENSION, 2013, 62 (06) :1013-1014
[9]   Dissimilar microRNA-21 functions and targets in trophoblastic cell lines of different origin [J].
Chaiwangyen, Wittaya ;
Ospina-Prieto, Stephanie ;
Photini, Stella Mary ;
Schleussner, Ekkehard ;
Markert, Udo R. ;
Morales-Prieto, Diana M. .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2015, 68 :187-196
[10]   miR-210: The Master Hypoxamir [J].
Chan, Yuk C. ;
Banerjee, Jaideep ;
Choi, Sang Yong ;
Sen, Chandan K. .
MICROCIRCULATION, 2012, 19 (03) :215-223