Insights into human endometrial receptivity from transcriptomic and proteomic data

被引:84
作者
Haouzi, Delphine [1 ,2 ,3 ]
Dechaud, Herve [1 ,2 ,3 ]
Assou, Said [1 ,2 ,3 ]
De Vos, John [1 ,3 ]
Hamamah, Samir [1 ,2 ,3 ]
机构
[1] Hop St Eloi, INSERM U847, Inst Rech Biotherapie, CHU Montpellier, F-34295 Montpellier 5, France
[2] Hop Arnaud de Villeneuve, Dept Med & Biol Reprod, ART PGD Div, CHU Montpellier, F-34295 Montpellier 5, France
[3] Univ Montpellier I, UFR Med, Lab Dev Embryonnaire Precoce & Cellules Souches E, F-34000 Montpellier, France
关键词
biomarkers; endometrial receptivity; IVF; omics; stimulated cycles; HUMAN CHORIONIC-GONADOTROPIN; CONTROLLED OVARIAN HYPERSTIMULATION; GENE-EXPRESSION PROFILES; IN-VITRO FERTILIZATION; GNRH ANTAGONIST; STIMULATED CYCLES; EMBRYONIC IMPLANTATION; UTERINE RECEPTIVITY; MONOAMINE-OXIDASE; MENSTRUAL-CYCLE;
D O I
10.1016/j.rbmo.2011.09.009
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
The appreciation of endometrial receptivity is a crucial step in assisted reproductive technology as implantation failures are thought to result, in large part, from abnormal endometrial receptivity. Using emerging omics technologies, investigators have begun to define both molecular signatures and specific biomarkers of receptive endometrium. The aim of this review was to analyse the new perspectives brought to the appreciation of endometrial receptivity by transcriptomic and proteomic technologies, involving the analysis of gene-or protein-expression-profile shifts between the pre-receptive and receptive secretory stages and how they might lead to new strategies for endometrial receptivity assessments. The use of omics as molecular tools to determine the effects of stimulation protocols on endometrial gene expression and clinical outcomes has also been investigated. (C) 2011, Reproductive Healthcare Ltd. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:23 / 34
页数:12
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