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Developing Potential Candidates of Preclinical Preeclampsia

The potential for developing molecules of interest in preclinical preeclampsia from candidate genes that were discovered on gene expression microarray analysis has been challenged by limited access to additional first trimester trophoblast and decidual tissues. The question of whether these candidat...

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Autores principales: Founds, Sandra, Zeng, Xuemei, Lykins, David, Roberts, James M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661881/
https://www.ncbi.nlm.nih.gov/pubmed/26580600
http://dx.doi.org/10.3390/ijms161126023
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author Founds, Sandra
Zeng, Xuemei
Lykins, David
Roberts, James M.
author_facet Founds, Sandra
Zeng, Xuemei
Lykins, David
Roberts, James M.
author_sort Founds, Sandra
collection PubMed
description The potential for developing molecules of interest in preclinical preeclampsia from candidate genes that were discovered on gene expression microarray analysis has been challenged by limited access to additional first trimester trophoblast and decidual tissues. The question of whether these candidates encode secreted proteins that may be detected in maternal circulation early in pregnancy has been investigated using various proteomic methods. Pilot studies utilizing mass spectrometry based proteomic assays, along with enzyme linked immunosorbent assays (ELISAs), and Western immunoblotting in first trimester samples are reported. The novel targeted mass spectrometry methods led to robust multiple reaction monitoring assays. Despite detection of several candidates in early gestation, challenges persist. Future antibody-based studies may lead to a novel multiplex protein panel for screening or detection to prevent or mitigate preeclampsia.
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spelling pubmed-46618812015-12-10 Developing Potential Candidates of Preclinical Preeclampsia Founds, Sandra Zeng, Xuemei Lykins, David Roberts, James M. Int J Mol Sci Article The potential for developing molecules of interest in preclinical preeclampsia from candidate genes that were discovered on gene expression microarray analysis has been challenged by limited access to additional first trimester trophoblast and decidual tissues. The question of whether these candidates encode secreted proteins that may be detected in maternal circulation early in pregnancy has been investigated using various proteomic methods. Pilot studies utilizing mass spectrometry based proteomic assays, along with enzyme linked immunosorbent assays (ELISAs), and Western immunoblotting in first trimester samples are reported. The novel targeted mass spectrometry methods led to robust multiple reaction monitoring assays. Despite detection of several candidates in early gestation, challenges persist. Future antibody-based studies may lead to a novel multiplex protein panel for screening or detection to prevent or mitigate preeclampsia. MDPI 2015-11-13 /pmc/articles/PMC4661881/ /pubmed/26580600 http://dx.doi.org/10.3390/ijms161126023 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Founds, Sandra
Zeng, Xuemei
Lykins, David
Roberts, James M.
Developing Potential Candidates of Preclinical Preeclampsia
title Developing Potential Candidates of Preclinical Preeclampsia
title_full Developing Potential Candidates of Preclinical Preeclampsia
title_fullStr Developing Potential Candidates of Preclinical Preeclampsia
title_full_unstemmed Developing Potential Candidates of Preclinical Preeclampsia
title_short Developing Potential Candidates of Preclinical Preeclampsia
title_sort developing potential candidates of preclinical preeclampsia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661881/
https://www.ncbi.nlm.nih.gov/pubmed/26580600
http://dx.doi.org/10.3390/ijms161126023
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