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G 蛋白偶联受体失调可能在重度子痫前期中发挥作用——胎盘基因表达谱的加权基因相关网络分析。

G-Protein Coupled Receptor Dysregulation May Play Roles in Severe Preeclampsia-A Weighted Gene Correlation Network Analysis of Placental Gene Expression Profile.

机构信息

College of Medicine, University of the Philippines, Manila 1000, Philippines.

Institute of Human Genetics, National Institutes of Health, University of the Philippines, Manila 1000, Philippines.

出版信息

Cells. 2022 Feb 22;11(5):763. doi: 10.3390/cells11050763.

DOI:10.3390/cells11050763
PMID:35269385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8909297/
Abstract

Preeclampsia is one of the major hypertensive diseases of pregnancy. Genetic factors contribute to abnormal placentation. The inadequate transformation of cytotrophoblasts causes failure of maternal spiral arteries' remodeling and results in narrow, atherotic-prone vessels, leading to relative placental ischemia. This study aims to explore the possibility of identifying dysregulated gene networks that may offer a potential target in the possible prevention of preeclampsia. We performed a weighted gene correlated network analysis (WGCNA) on a subset of gene expression profiles of placental tissues from severe preeclamptic pregnancies. We identified a gene module (number of genes = 402, GS = 0.35, = 0.02) enriched for several G-protein-coupled receptor (GPCR)-related genes with significant protein-protein molecular interaction (number of genes = 38, FDR = 0.0007) that may play key roles in preeclampsia. Some genes are noted to play key roles in preeclampsia, including , and , whose functions generally relate to angiogenesis and vasodilation or vasoconstriction. Other upregulated genes, including olfactory and orexigenic genes, serve limited functions in the disease pathogenesis. Altogether, this study shows the utility of WGCNA in exploring possible new gene targets, and additionally reinforces the feasibility of targeting GPCRs that may offer intervention against development and disease progression among severe preeclampsia patients.

摘要

子痫前期是妊娠高血压疾病的主要类型之一。遗传因素导致胎盘异常。滋养细胞的不完全转化导致母体螺旋动脉重塑失败,导致血管狭窄、易发生动脉粥样硬化,从而导致相对胎盘缺血。本研究旨在探讨识别失调基因网络的可能性,这些网络可能为预防子痫前期提供潜在靶点。我们对严重子痫前期妊娠胎盘组织的基因表达谱进行了加权基因相关网络分析(WGCNA)。我们鉴定了一个基因模块(基因数量=402,GS=0.35,=0.02),其中富集了几个 G 蛋白偶联受体(GPCR)相关基因,这些基因具有显著的蛋白质-蛋白质分子相互作用(基因数量=38,FDR=0.0007),这些基因可能在子痫前期中发挥关键作用。一些基因被认为在子痫前期中发挥关键作用,包括、和,它们的功能通常与血管生成和血管舒张或血管收缩有关。其他上调的基因,包括嗅觉和食欲基因,在疾病发病机制中发挥有限的作用。总之,本研究表明 WGCNA 可用于探索可能的新基因靶点,并进一步证实靶向 GPCR 可能为严重子痫前期患者的发展和疾病进展提供干预措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f80e/8909297/29f90e7f6008/cells-11-00763-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f80e/8909297/6b6dc2b89e21/cells-11-00763-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f80e/8909297/5cced633a771/cells-11-00763-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f80e/8909297/29f90e7f6008/cells-11-00763-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f80e/8909297/6b6dc2b89e21/cells-11-00763-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f80e/8909297/5cced633a771/cells-11-00763-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f80e/8909297/29f90e7f6008/cells-11-00763-g003.jpg

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Potential genetic biomarkers predict adverse pregnancy outcome during early and mid-pregnancy in women with systemic lupus erythematosus.
潜在的遗传生物标志物可预测系统性红斑狼疮女性在早中期妊娠的不良妊娠结局。
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