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22 January 2018 An update on the progress of transcriptomic profiles of human endometrial receptivity
Xi Wang, Qi Yu
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Abstract

Despite advances in our understanding of fertility, implantation failure remains a significant problem for both spontaneous and assisted pregnancies. Most research efforts concerning the process of implantation are embryo-centric, with a dearth of studies on endometrial factors. Currently, there are no practical and effective diagnostic tools available to precisely predict endometrial receptivity. Transcriptomics, a field based on microarray technology, has a number of procedures for clinical applications, although the functional relevance of most identified genes remains unclear. Importantly, RNA sequencing will further improve the precision and broaden the clinical use of the transcriptome by detecting previously undiscovered genes, which could be used to further our understanding of endometrial receptivity. In this review, potential biomarkers based on endometrium gene expression profiles of human endometrial receptivity were described and compared in natural and stimulated cycles toward discovering future prospects for personalized medical approaches. The intent of this synthesis is to provide researchers, doctors, and clinicians in the field with a better understanding of endometrium receptivity, promote further study in the transcriptome in embryo implantation, and ultimately, improve pregnancy outcome.

Summary Sentence

Transcriptomics is emerging as a powerful tool to identify potential molecular biomarkers for endometrial receptivity, thereby improving forecasts of pregnancy outcome during in vitro fertilization treatment.

© The Author(s) 2018. Published by Oxford University Press on behalf of Society for the Study of Reproduction. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com
Xi Wang and Qi Yu "An update on the progress of transcriptomic profiles of human endometrial receptivity," Biology of Reproduction 98(4), 440-448, (22 January 2018). https://doi.org/10.1093/biolre/ioy018
Received: 10 November 2017; Accepted: 19 January 2018; Published: 22 January 2018
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