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The placenta in preeclampsia.子痫前期中的胎盘。
Pregnancy Hypertens. 2012 Apr 1;2(2):72-83. doi: 10.1016/j.preghy.2012.01.001.
2
Maternal superobesity and perinatal outcomes.母亲肥胖与围产期结局。
Am J Obstet Gynecol. 2012 May;206(5):417.e1-6. doi: 10.1016/j.ajog.2012.02.037. Epub 2012 Mar 7.
3
Associations of the pre-pregnancy body mass index and gestational weight gain with pregnancy outcomes in Taiwanese women.台湾女性孕前体重指数和孕期体重增加与妊娠结局的关联。
Asia Pac J Clin Nutr. 2012;21(1):82-7.
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Loss of secreted frizzled-related protein 4 correlates with an aggressive phenotype and predicts poor outcome in ovarian cancer patients.分泌型卷曲相关蛋白 4 的缺失与卵巢癌患者侵袭性表型相关,并预示不良预后。
PLoS One. 2012;7(2):e31885. doi: 10.1371/journal.pone.0031885. Epub 2012 Feb 21.
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Preeclampsia: multiple approaches for a multifactorial disease.子痫前期:一种多因素疾病的多种方法。
Dis Model Mech. 2012 Jan;5(1):9-18. doi: 10.1242/dmm.008516.
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A novel 3-arylethynyl-substituted pyrido[2,3,-b]pyrazine derivatives and pharmacophore model as Wnt2/β-catenin pathway inhibitors in non-small-cell lung cancer cell lines.一种新型 3-芳基乙炔基取代的吡啶并[2,3,-b]哒嗪衍生物及其作为非小细胞肺癌细胞系中 Wnt2/β-连环蛋白通路抑制剂的药效团模型。
Bioorg Med Chem. 2011 Sep 15;19(18):5639-47. doi: 10.1016/j.bmc.2011.07.028. Epub 2011 Jul 23.
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Wnt2 secreted by tumour fibroblasts promotes tumour progression in oesophageal cancer by activation of the Wnt/β-catenin signalling pathway.肿瘤成纤维细胞分泌的 Wnt2 通过激活 Wnt/β-catenin 信号通路促进食管癌的肿瘤进展。
Gut. 2011 Dec;60(12):1635-43. doi: 10.1136/gut.2011.241638. Epub 2011 Jun 14.
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Multiplexed methylation profiles of tumor suppressor genes and clinical outcome in lung cancer.肺癌中肿瘤抑制基因的多重甲基化谱与临床结局。
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Wnt signalling in implantation, decidualisation and placental differentiation--review.Wnt 信号在着床、蜕膜化和胎盘分化中的作用——综述。
Placenta. 2010 Oct;31(10):839-47. doi: 10.1016/j.placenta.2010.07.011. Epub 2010 Aug 15.
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[Pregnancy hypertension].[妊娠高血压]
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在重度子痫前期孕妇的胎盘第三孕期中 Wnt2 和 sFRP4 表达的相关性。

Association of Wnt2 and sFRP4 expression in the third trimester placenta in women with severe preeclampsia.

机构信息

Department of Clinical Laboratory, The Third Affiliated Hospital of Zhengzhou University, No. 7 Front Kangfu Street, Zhengzhou, Henan, China.

出版信息

Reprod Sci. 2013 Aug;20(8):981-9. doi: 10.1177/1933719112472740. Epub 2013 Jan 15.

DOI:10.1177/1933719112472740
PMID:23322712
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3713648/
Abstract

BACKGROUND

The Wnt signaling pathway is a conserved pathway and plays a crucial role in regulating trophoblast functions. Abnormal expression of the Wnt pathway may result in the dysfunction of the trophoblast that can contribute to the pathogenesis of preeclampsia (PE). However, published data regarding the association between Wnt pathway and PE in human pregnancy is rare.

OBJECTIVE

The aims of this study were to investigate the expression pattern of Wnt2 and secreted frizzled-related protein 4 (sFRP4) in the third trimester human placenta and to evaluate the relationship between changes in placental Wnt2 and sFRP4 expression and severe PE.

METHODS

The expression of Wnt2 and sFRP4 in normal and severe PE placentas was examined using immunohistochemistry (IHC), real-time polymerase chain reaction, and Western blot.

RESULTS

Compared to the controls, the relative expression of Wnt2 messenger RNA was remarkably downregulated in the PE placentas, while there was no significant difference in sFRP4 between the 2 groups. The IHC indicated that Wnt2 and sFRP4 were expressed predominantly in the villous syncytiotrophoblast and the extravillous trophoblast, whereas Wnt2 in the control group showed higher staining intensity than in the PE group, and sFRP4 in the PE group had a higher staining intensity than in the control group. Furthermore, the results of the Western blots were consistent with the IHC.

CONCLUSIONS

The Wnt signaling pathway was detected in human third trimester placentas, and the decreased placental expression of Wnt2 and increased placental expression of sFRP4 may be associated with the pathogenesis of severe PE.

摘要

背景

Wnt 信号通路是一条保守的通路,在调节滋养细胞功能方面起着至关重要的作用。Wnt 通路的异常表达可能导致滋养细胞功能障碍,从而导致子痫前期(PE)的发病机制。然而,关于人类妊娠中 Wnt 通路与 PE 之间的关联的已发表数据很少。

目的

本研究旨在探讨 Wnt2 和分泌型卷曲相关蛋白 4(sFRP4)在妊娠晚期人胎盘中的表达模式,并评估胎盘 Wnt2 和 sFRP4 表达变化与重度 PE 的关系。

方法

采用免疫组织化学(IHC)、实时聚合酶链反应和 Western blot 检测正常和重度 PE 胎盘中 Wnt2 和 sFRP4 的表达。

结果

与对照组相比,PE 胎盘中 Wnt2 信使 RNA 的相对表达显著下调,而两组之间 sFRP4 无显著差异。IHC 表明 Wnt2 和 sFRP4 主要表达于绒毛合体滋养细胞和绒毛外滋养细胞,而对照组中 Wnt2 的染色强度高于 PE 组,PE 组中 sFRP4 的染色强度高于对照组。此外,Western blot 的结果与 IHC 一致。

结论

在人类妊娠晚期胎盘检测到 Wnt 信号通路,胎盘 Wnt2 表达降低和 sFRP4 表达增加可能与重度 PE 的发病机制有关。