TY - JOUR
T1 - The transcriptome of cervical ripening in human pregnancy before the onset of labor at term
T2 - Identification of novel molecular functions involved in this process
AU - Hassan, Sonia S.
AU - Romero, Roberto
AU - Tarca, Adi L.
AU - Nhan-Chang, Chia Ling
AU - Vaisbuch, Edi
AU - Erez, Offer
AU - Mittal, Pooja
AU - Kusanovic, Juan Pedro
AU - Mazaki-Tovi, Shali
AU - Yeo, Lami
AU - Draghici, Sorin
AU - Kim, Jung Sun
AU - Uldbjerg, Niels
AU - Kim, Chong Jai
PY - 2009/12
Y1 - 2009/12
N2 - The aim of this study was to identify changes in the cervical transcriptome in the human uterine cervix as a function of ripening before the onset of labor. Study Design. Human cervical tissue was obtained from women at term not in labor with ripe (n=11) and unripe (n=11) cervices and profiled using Affymetrix GeneChip® HGU133Plus2.0 arrays. Gene expression was analyzed using a moderated t-test (False Discovery Rate 5%). Gene ontology and pathway analysis were performed. Quantitative reverse transcription-polymerase chain reaction (qRT-PCR) was used for confirmation of selected differentially expressed genes. Results. (1) Ninety-one genes were differentially expressed between ripe and unripe groups. (2) Cervical ripening was associated with enrichment of specific biological processes (e.g. cell adhesion, regulation of anatomical structure), pathways and 11 molecular functions (e.g. extracelluar matrix (ECM)-structural constituent, protein binding, glycosaminoglycan binding). (3) qRT-PCR confirmed that 9 of 11 tested differentially expressed genes (determined by microarray) were upregulated in a ripe cervix (e.g. MYOCD, VCAN, THBS1, COL5A1). (4) Twenty-three additional genes related to ECM metabolism and adhesion molecules were differentially regulated (by qRT-PCR) in ripe cervices. Conclusion. (1) This is the first description of the changes in the human cervical transcriptome with ripening before the onset of labor. (2) Biological processes, pathways and molecular functions were identified with the use of this unbiased approach. (3) In contrast to cervical dilation after term labor, inflammation-related genes did not emerge as differentially regulated with cervical ripening. (4) Myocardin was identified as a novel gene upregulated in human cervical ripening.
AB - The aim of this study was to identify changes in the cervical transcriptome in the human uterine cervix as a function of ripening before the onset of labor. Study Design. Human cervical tissue was obtained from women at term not in labor with ripe (n=11) and unripe (n=11) cervices and profiled using Affymetrix GeneChip® HGU133Plus2.0 arrays. Gene expression was analyzed using a moderated t-test (False Discovery Rate 5%). Gene ontology and pathway analysis were performed. Quantitative reverse transcription-polymerase chain reaction (qRT-PCR) was used for confirmation of selected differentially expressed genes. Results. (1) Ninety-one genes were differentially expressed between ripe and unripe groups. (2) Cervical ripening was associated with enrichment of specific biological processes (e.g. cell adhesion, regulation of anatomical structure), pathways and 11 molecular functions (e.g. extracelluar matrix (ECM)-structural constituent, protein binding, glycosaminoglycan binding). (3) qRT-PCR confirmed that 9 of 11 tested differentially expressed genes (determined by microarray) were upregulated in a ripe cervix (e.g. MYOCD, VCAN, THBS1, COL5A1). (4) Twenty-three additional genes related to ECM metabolism and adhesion molecules were differentially regulated (by qRT-PCR) in ripe cervices. Conclusion. (1) This is the first description of the changes in the human cervical transcriptome with ripening before the onset of labor. (2) Biological processes, pathways and molecular functions were identified with the use of this unbiased approach. (3) In contrast to cervical dilation after term labor, inflammation-related genes did not emerge as differentially regulated with cervical ripening. (4) Myocardin was identified as a novel gene upregulated in human cervical ripening.
KW - ADAMTS
KW - Cell adhesion
KW - Cervix
KW - Collagen
KW - Extracellular matrix structural constituent
KW - Integrin binding
KW - Matrix metalloproteinase
KW - Regulation of anatomical structure
KW - Regulation of locomotion
KW - Ripe cervix
KW - Structural molecule activity
KW - Versican
UR - http://www.scopus.com/inward/record.url?scp=73949136096&partnerID=8YFLogxK
U2 - 10.3109/14767050903353216
DO - 10.3109/14767050903353216
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 19883264
AN - SCOPUS:73949136096
SN - 1476-7058
VL - 22
SP - 1183
EP - 1193
JO - Journal of Maternal-Fetal and Neonatal Medicine
JF - Journal of Maternal-Fetal and Neonatal Medicine
IS - 12
ER -