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Characterization of the transcriptome of chorioamniotic membranes at the site of rupture in spontaneous labor at term.

Authors :
Nhan-Chang CL
Romero R
Tarca AL
Mittal P
Kusanovic JP
Erez O
Mazaki-Tovi S
Chaiworapongsa T
Hotra J
Than NG
Kim JS
Hassan SS
Kim CJ
Source :
American journal of obstetrics and gynecology [Am J Obstet Gynecol] 2010 May; Vol. 202 (5), pp. 462.e1-41.
Publication Year :
2010

Abstract

Objective: The purpose of this study was to compare the transcriptome between the site of membrane rupture and the chorioamniotic membranes away from the site of rupture.<br />Study Design: The transcriptome of amnion and chorion (n=20 each) from and distal to the site of rupture from women with spontaneous labor and vaginal delivery at term after spontaneous rupture of membranes was profiled with Illumina HumanHT-12 microarrays. Selected genes were validated with the use of quantitative reverse transcription-polymerase chain reaction.<br />Results: Six hundred seventy-seven genes were differentially expressed in the chorion between the rupture and nonrupture sites (false discovery rate<0.1; fold change>1.5). Quantitative reverse transcription-polymerase chain reaction confirmed the differential expression in 10 of 14 genes. Enriched biological processes included anatomic structure development, cell adhesion and signal transduction. Extracellular matrix-receptor interaction was the most impacted signaling pathway.<br />Conclusion: The transcriptome of fetal membranes after spontaneous rupture of membranes in term labor is characterized by region- and tissue-specific differential expression of genes that are involved in signature pathways, which include extracellular matrix-receptor interactions.<br /> (Copyright (c) 2010 Mosby, Inc. All rights reserved.)

Details

Language :
English
ISSN :
1097-6868
Volume :
202
Issue :
5
Database :
MEDLINE
Journal :
American journal of obstetrics and gynecology
Publication Type :
Academic Journal
Accession number :
20452490
Full Text :
https://doi.org/10.1016/j.ajog.2010.02.045