Volume 203, Issue 5 , Pages 472.e1-472.e14, November 2010
The molecular basis for sonographic cervical shortening at term: identification of differentially expressed genes and the epithelial-mesenchymal transition as a function of cervical length
Objective
The purpose of this study was to determine whether cervical shortening of a ripe cervix at term is associated with changes in the cervical transcriptome.
Study Design
Sonographically measured cervical lengths and biopsy specimens were obtained from 19 women at term who were not in labor with a ripe cervix. Affymetrix HG-U133 Plus 2.0 arrays (Affymetrix Inc, Santa Clara, CA) were used. Gene expression was analyzed as a function of cervical length. Gene Ontology, pathway analyses, quantitative real-time reverse transcription–polymerase chain reaction, and immunohistochemistry were performed.
Results
Cervical length shortening was associated with differential expression of 687 genes. Fifty-four biologic processes, 22 molecular functions, and 9 pathways were enriched. Quantitative real-time reverse transcription–polymerase chain reaction analysis confirmed differential expression of 13 genes. Bone morphogenetic protein-7, claudin-1, integrin beta-6, and endometrial progesterone–induced protein messenger RNA, and protein expressions were down-regulated with cervical shortening.
Conclusion
Sonographic cervical shortening in patients at term who are not in labor with a ripe cervix is associated with changes in the uterine cervix transcriptome. The epithelial-mesenchymal transition may participate in the mechanism of cervical shortening at term.
Key words: bone morphogenetic protein 7 (BMP-7), cervical length, cervical ripening, claudin-1, endometrial progesterone-induced protein (EPIP), epithelial-mesenchymal transition, extracellular matrix, high-dimensional biology, preterm birth, progesterone, PSAT1, tight junction, transforming growth factor-beta (TGF-β), uterine cervix
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Authorship and contribution to the article is limited to the 12 authors indicated. There was no outside funding or technical assistance with the production of this article.
Cite this article as: Hassan SS, Romero R, Tarca AL, et al. The molecular basis for sonographic cervical shortening at term: identification of differentially expressed genes and the epithelial-mesenchymal transition as a function of cervical length. Am J Obstet Gynecol 2010;203:472.e1-14.
PII: S0002-9378(10)00856-2
doi:10.1016/j.ajog.2010.06.076
© 2010 Mosby, Inc. All rights reserved.
Volume 203, Issue 5 , Pages 472.e1-472.e14, November 2010
