Distinct cervical microRNA profiles are present in women destined to have a preterm birth

被引:60
作者
Elovitz, Michal A. [1 ]
Brown, Amy G. [1 ]
Anton, Lauren [1 ]
Gilstrop, Marisa [1 ]
Heiser, Laura [1 ]
Bastek, Jamie [1 ]
机构
[1] Univ Penn, Dept Obstet & Gynecol, Perelman Sch Med, Maternal Child Hlth Res Program, Philadelphia, PA 19104 USA
关键词
cervical remodeling; ectocervical cells; microRNA; preterm birth; TROPHOBLAST INVASION; MIR-143/145; CLUSTER; EPITHELIAL BARRIER; HUMAN-PREGNANCY; DYNAMIC CHANGES; DOUBLE-BLIND; RISK; PROGESTERONE; DIFFERENTIATION; CONTRACTILITY;
D O I
10.1016/j.ajog.2013.12.043
中图分类号
R71 [妇产科学];
学科分类号
100211 [妇产科学];
摘要
OBJECTIVE: Although premature cervical remodeling is involved in preterm birth (PTB), the molecular pathways that are involved have not been elucidated fully. MicroRNAs (miRNAs) that are highly conserved single-stranded noncoding RNAs that play a crucial role in gene regulation have now been identified as important players in disease states. The objective of this study was to determine whether miRNA profiles in cervical cells are different in women who are destined to have a PTB compared with a term birth. STUDY DESIGN: A nested case-control study was performed. With the use of a noninvasive method, cervical cells were obtained at 2 time points in pregnancy. The cervical cell miRNA expression profiles were compared between women who ultimately had a PTB (n = 10) compared with a term birth (n = 10). MiRNA expression profiles were created with the Affymetrix GeneChip miRNA Array. The data were analyzed with the Significance of Analysis of Microarrays and Principle Components Analyses. A false-discovery rate of 20% was used to determine the most differentially expressed miRNAs. Validation was performed with quantitative polymerase chain reaction. In vitro studies were performed to confirm expression and regulation of select miRNAs. RESULTS: With a false-discovery rate of 20% of the 5640 miRNAs that were analyzed on the array, 99 miRNAs differed between those with a PTB vs a term birth. Qualitative polymerase chain reaction validated the array findings. In vitro studies confirmed expression of select miRNAs in cervical cells. CONCLUSION: MiRNA profiles in cervical cells may distinguish women who are at risk for PTB months before the outcome. With the large downstream effects of miRNAs on gene expression, these studies provide a new understanding of the processes that are involved in premature cervical remodeling and allow for the discovery of new therapeutic targets.
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页数:11
相关论文
共 56 条
[1]
Differential Expression of MicroRNAs in Different Disease States [J].
Abdellatif, Maha .
CIRCULATION RESEARCH, 2012, 110 (04) :638-650
[2]
Dynamic Changes in Cervical Glycosaminoglycan Composition during Normal Pregnancy and Preterm Birth [J].
Akgul, Yucel ;
Holt, Roxane ;
Mummert, Mark ;
Word, Ann ;
Mahendroo, Mala .
ENDOCRINOLOGY, 2012, 153 (07) :3493-3503
[3]
Can microRNAs control vascular smooth muscle phenotypic modulation and the response to injury? [J].
Albinsson, Sebastian ;
Sessa, William C. .
PHYSIOLOGICAL GENOMICS, 2011, 43 (10) :529-533
[4]
Role of MicroRNAs in Lung Disease [J].
Angulo, Martin ;
Lecuona, Emilia ;
Iasha Sznajder, Jacob .
ARCHIVOS DE BRONCONEUMOLOGIA, 2012, 48 (09) :325-330
[5]
[Anonymous], AM J OBSTET GYNECOL
[6]
miR-210 Inhibits Trophoblast Invasion and Is a Serum Biomarker for Preedampsia [J].
Anton, Lauren ;
Olarerin-George, Anthony O. ;
Schwartz, Nadav ;
Srinivas, Sindhu ;
Bastek, Jamie ;
Hogenesch, John B. ;
Elovitz, Michal A. .
AMERICAN JOURNAL OF PATHOLOGY, 2013, 183 (05) :1437-1445
[7]
Lipopolysaccharide induces cytokine production and decreases extravillous trophoblast invasion through a mitogen-activated protein kinase-mediated pathway: possible mechanisms of first trimester placental dysfunction [J].
Anton, Lauren ;
Brown, Amy G. ;
Parry, Samuel ;
Elovitz, Michal A. .
HUMAN REPRODUCTION, 2012, 27 (01) :61-72
[8]
Biomarkers and Cervical Length to Predict Spontaneous Preterm Birth in Asymptomatic High-Risk Women [J].
Bastek, Jamie A. ;
Hirshberg, Adi ;
Chandrasekaran, Suchitra ;
Owen, Carter M. ;
Heiser, Laura M. ;
Araujo, Brittany A. ;
McShea, Meghan A. ;
Ryan, Meghan E. ;
Elovitz, Michal A. .
OBSTETRICS AND GYNECOLOGY, 2013, 122 (02) :283-289
[9]
Inhibition of the miR-143/145 cluster attenuated neutrophil differentiation of APL cells [J].
Batliner, Jasmin ;
Buehrer, Emanuel ;
Fey, Martin F. ;
Tschan, Mario P. .
LEUKEMIA RESEARCH, 2012, 36 (02) :237-240
[10]
Effects of the miR-143/-145 MicroRNA Cluster on the Colon Cancer Proteome and Transcriptome [J].
Bauer, Kerry M. ;
Hummon, Amanda B. .
JOURNAL OF PROTEOME RESEARCH, 2012, 11 (09) :4744-4754