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Molecular signatures of labor and nonlabor myometrium with parsimonious classification from 2 calcium transporter genes

Clinical phenotyping of term and preterm labor is imprecise, and disagreement persists on categorization relative to underlying pathobiology, which remains poorly understood. We performed RNA sequencing (RNA-seq) of 31 specimens of human uterine myometrium from 10 term and 21 preterm cesarean delive...

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Autores principales: Ackerman, William E., Buhimschi, Catalin S., Snedden, Ali, Summerfield, Taryn L., Zhao, Guomao, Buhimschi, Irina A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Clinical Investigation 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8262336/
https://www.ncbi.nlm.nih.gov/pubmed/33945511
http://dx.doi.org/10.1172/jci.insight.148425
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author Ackerman, William E.
Buhimschi, Catalin S.
Snedden, Ali
Summerfield, Taryn L.
Zhao, Guomao
Buhimschi, Irina A.
author_facet Ackerman, William E.
Buhimschi, Catalin S.
Snedden, Ali
Summerfield, Taryn L.
Zhao, Guomao
Buhimschi, Irina A.
author_sort Ackerman, William E.
collection PubMed
description Clinical phenotyping of term and preterm labor is imprecise, and disagreement persists on categorization relative to underlying pathobiology, which remains poorly understood. We performed RNA sequencing (RNA-seq) of 31 specimens of human uterine myometrium from 10 term and 21 preterm cesarean deliveries with rich clinical context information. A molecular signature of 4814 transcripts stratified myometrial samples into quiescent (Q) and nonquiescent (NQ) phenotypes, independent of gestational age and incision site. Similar stratifications were achieved using expressed genes in Ca(2+) signaling and TGF-β pathways. For maximal parsimony, we evaluated the expression of just 2 Ca(2+) transporter genes, ATP2B4 (encoding PMCA4) and ATP2A2 (coding for SERCA2), and we found that their ratio reliably distinguished NQ and Q specimens in the current study, and also in 2 publicly available RNA-seq data sets (GSE50599 and GSE80172), with an overall AUC of 0.94. Cross-validation of the ATP2B4/ATP2A2 ratio by quantitative PCR in an expanded cohort (by 11 additional specimens) achieved complete separation (AUC of 1.00) of NQ versus Q specimens. While providing additional insight into the associations between clinical features of term and preterm labor and myometrial gene expression, our study also offers a practical algorithm for unbiased classification of myometrial biopsies by their overall contractile program.
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spelling pubmed-82623362021-07-13 Molecular signatures of labor and nonlabor myometrium with parsimonious classification from 2 calcium transporter genes Ackerman, William E. Buhimschi, Catalin S. Snedden, Ali Summerfield, Taryn L. Zhao, Guomao Buhimschi, Irina A. JCI Insight Research Article Clinical phenotyping of term and preterm labor is imprecise, and disagreement persists on categorization relative to underlying pathobiology, which remains poorly understood. We performed RNA sequencing (RNA-seq) of 31 specimens of human uterine myometrium from 10 term and 21 preterm cesarean deliveries with rich clinical context information. A molecular signature of 4814 transcripts stratified myometrial samples into quiescent (Q) and nonquiescent (NQ) phenotypes, independent of gestational age and incision site. Similar stratifications were achieved using expressed genes in Ca(2+) signaling and TGF-β pathways. For maximal parsimony, we evaluated the expression of just 2 Ca(2+) transporter genes, ATP2B4 (encoding PMCA4) and ATP2A2 (coding for SERCA2), and we found that their ratio reliably distinguished NQ and Q specimens in the current study, and also in 2 publicly available RNA-seq data sets (GSE50599 and GSE80172), with an overall AUC of 0.94. Cross-validation of the ATP2B4/ATP2A2 ratio by quantitative PCR in an expanded cohort (by 11 additional specimens) achieved complete separation (AUC of 1.00) of NQ versus Q specimens. While providing additional insight into the associations between clinical features of term and preterm labor and myometrial gene expression, our study also offers a practical algorithm for unbiased classification of myometrial biopsies by their overall contractile program. American Society for Clinical Investigation 2021-06-08 /pmc/articles/PMC8262336/ /pubmed/33945511 http://dx.doi.org/10.1172/jci.insight.148425 Text en © 2021 Ackerman et al. https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Ackerman, William E.
Buhimschi, Catalin S.
Snedden, Ali
Summerfield, Taryn L.
Zhao, Guomao
Buhimschi, Irina A.
Molecular signatures of labor and nonlabor myometrium with parsimonious classification from 2 calcium transporter genes
title Molecular signatures of labor and nonlabor myometrium with parsimonious classification from 2 calcium transporter genes
title_full Molecular signatures of labor and nonlabor myometrium with parsimonious classification from 2 calcium transporter genes
title_fullStr Molecular signatures of labor and nonlabor myometrium with parsimonious classification from 2 calcium transporter genes
title_full_unstemmed Molecular signatures of labor and nonlabor myometrium with parsimonious classification from 2 calcium transporter genes
title_short Molecular signatures of labor and nonlabor myometrium with parsimonious classification from 2 calcium transporter genes
title_sort molecular signatures of labor and nonlabor myometrium with parsimonious classification from 2 calcium transporter genes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8262336/
https://www.ncbi.nlm.nih.gov/pubmed/33945511
http://dx.doi.org/10.1172/jci.insight.148425
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