Gene markers of normal villous maturation and their expression in placentas with maturational pathology

被引:21
作者
Leavey, Katherine [1 ]
Benton, Samantha J. [2 ]
Grynspan, David [3 ]
Bainbridge, Shannon A. [2 ,4 ]
Morgen, Eric K. [5 ,6 ]
Cox, Brian J. [1 ,7 ]
机构
[1] Univ Toronto, Dept Physiol, Med Sci Bldg,Room 3360,1 Kings Coll Circle, Toronto, ON M5S 1A8, Canada
[2] Univ Ottawa, Dept Cellular & Mol Med, Ottawa, ON, Canada
[3] Univ Ottawa, Dept Pathol & Lab Med, Ottawa, ON, Canada
[4] Univ Ottawa, Interdisciplinary Sch Hlth Sci, Ottawa, ON, Canada
[5] Mt Sinai Hosp, Dept Pathol & Lab Med, Ottawa, ON, Canada
[6] Univ Toronto, Dept Lab Med & Pathobiol, Ottawa, ON, Canada
[7] Univ Toronto, Dept Obstet & Gynaecol, Ottawa, ON, Canada
基金
加拿大健康研究院;
关键词
Advanced villous maturity; Delayed villous maturity; Gene signature; Histology; Microarray; Placenta; PREGNANCY; GROWTH; TREE;
D O I
10.1016/j.placenta.2017.08.005
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Introduction: The placenta demonstrates a recognized sequence of histomorphologic maturation throughout pregnancy, and in some cases, shows abnormally advanced (AVM) or delayed (DVM) villous maturation. While AVM and DVM have important clinical implications, it is unknown whether they truly represent a state of accelerated/delayed normal maturation or a state of pathological maldevelopment. The purpose of our study is, therefore, to address this challenge via a genome-wide search for expression markers of normal villous maturation (NM) and the assessment of these genes in cases of maturational pathology. Methods: A total of 142 placentas, previously evaluated by gene expression microarray, were reviewed histologically and classified as NM, AVM, or DVM. Expression data from healthy NM placentas underwent Pearson correlations with gestational age (GA) and network/pathway analysis to identify candidate gene markers. Candidates were then validated in an independent microarray dataset and used to calculate "molecular GAs" of placentas with maturational pathology. Results: Analysis of NM placentas yielded 17 candidate markers of normal villous maturation, of which 11 were independently validated. Genes with expression increasing across gestation were associated with transcription and metabolism, while those demonstrating decreasing expression were involved in cell cycle and division. Molecular GAwas 5.3 weeks older than true GA among AVM placentas (p < 0.001), and 1.1 weeks younger among DVM placentas (p = 0.149). Discussion: We have found evidence of advanced molecular GA in AVM placentas, while molecular alterations in DVM placentas were merely suggestive of delayed maturation. In the future, these findings will need to be validated with additional techniques such as in situ hybridization or immunohistochemistry. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:52 / 59
页数:8
相关论文
共 22 条
[1]  
[Anonymous], POTTERS PATHOLOGY FE
[2]  
CASTELLUCCI M, 1990, ANAT EMBRYOL, V181, P117
[3]   VILLOUS IMMATURITY IN TERM PLACENTA [J].
FOX, H .
OBSTETRICS AND GYNECOLOGY, 1968, 31 (01) :9-&
[4]   Report of the National High Blood Pressure Education Program Working Group on High Blood Pressure in Pregnancy [J].
Gifford, RW ;
August, PA ;
Cunningham, G ;
Green, LA ;
Lindheimer, MD ;
McNellis, D ;
Roberts, JM ;
Sibai, BM ;
Taler, SJ .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2000, 183 (01) :S1-S22
[5]   Clinical Associations with a Placental Diagnosis of Delayed Villous Maturation: A Retrospective Study [J].
Higgins, Mary ;
McAuliffe, Fionnuala M. ;
Mooney, Eoghan E. .
PEDIATRIC AND DEVELOPMENTAL PATHOLOGY, 2011, 14 (04) :273-279
[6]   Sampling and Definitions of Placental Lesions Amsterdam Placental Workshop Group Consensus Statement [J].
Khong, T. Yee ;
Mooney, Eoghan E. ;
Ariel, Ilana ;
Balmus, Nathalie C. M. ;
Boyd, Theonia K. ;
Brundler, Marie-Anne ;
Derricott, Hayley ;
Evans, Margaret J. ;
Faye-Petersen, Ona M. ;
Gillan, John E. ;
Heazell, Alex E. P. ;
Heller, Debra S. ;
Jacques, Suzanne M. ;
Keating, Sarah ;
Kelehan, Peter ;
Maes, Ann ;
McKay, Eileen M. ;
Morgan, Terry K. ;
Nikkels, Peter G. J. ;
Parks, W. Tony ;
Redline, Raymond W. ;
Scheimberg, Irene ;
Schoots, Mirthe H. ;
Sebire, Neil J. ;
Timmer, Albert ;
Turowski, Gitta ;
van der Voorn, J. Patrick ;
van Lijnschoten, Ineke ;
Gordijn, Sanne J. .
ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE, 2016, 140 (07) :698-713
[7]   Oxygen and placental villous development: Origins of fetal hypoxia [J].
Kingdom, JCP ;
Kaufmann, P .
PLACENTA, 1997, 18 (08) :613-621
[8]   Intrauterine growth restriction with absent end-diastolic flow velocity in the umbilical artery is associated with maldevelopment of the placental terminal villous tree [J].
Krebs, C ;
Macara, LM ;
Leiser, R ;
Bowman, AW ;
Greer, IA ;
Kingdom, JCP .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1996, 175 (06) :1534-1542
[9]   WGCNA: an R package for weighted correlation network analysis [J].
Langfelder, Peter ;
Horvath, Steve .
BMC BIOINFORMATICS, 2008, 9 (1)
[10]   Unsupervised Placental Gene Expression Profiling Identifies Clinically Relevant Subclasses of Human Preeclampsia [J].
Leavey, Katherine ;
Benton, Samantha J. ;
Grynspan, David ;
Kingdom, John C. ;
Bainbridge, Shannon A. ;
Cox, Brian J. .
HYPERTENSION, 2016, 68 (01) :137-+