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通过 DNA 微阵列鉴定子痫前期妊娠与正常妊娠胎盘的差异基因表达谱。

Identification of differential gene expression profiles in placentas from preeclamptic pregnancies versus normal pregnancies by DNA microarrays.

机构信息

Department of Obstetrics, The First Affiliated Hospital of China Medical University, Shenyang, People's Republic of China.

出版信息

OMICS. 2012 Jun;16(6):301-11. doi: 10.1089/omi.2011.0066.

DOI:10.1089/omi.2011.0066
PMID:22702245
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3369279/
Abstract

The purpose of this study was to perform a comprehensive analysis of gene expression profiles in placentas from preeclamptic pregnancies versus normal placentas. Placental tissues were obtained immediately after delivery from women with normal pregnancies (n=6) and patients with preeclampsia (n=6). The gene expression profile was assessed by oligonucleotide-based DNA microarrays and validated by quantitative real-time RT-PCR. Functional relationships and canonical pathways/networks of differentially-expressed genes were evaluated by GeneSpring™ GX 11.0 software, and ingenuity pathways analysis (IPA). A total of 939 genes were identified that differed significantly in expression: 483 genes were upregulated and 456 genes were downregulated in preeclamptic placentas compared with normal placentas (fold change ≥ 2 and p<0.05 by unpaired t-test corrected with Bonferroni multiple testing). The IPA revealed that the primary molecular functions of these genes are involved in cellular function and maintenance, cellular development, cell signaling, and lipid metabolism. Pathway analysis provided evidence that a number of biological pathways, including Notch, Wnt, NF-κB, and transforming growth factor-β (TGF-β) signaling pathways, were aberrantly regulated in preeclampsia. In conclusion, our microarray analysis represents a comprehensive list of placental gene expression profiles and various dysregulated signaling pathways that are altered in preeclampsia. These observations may provide the basis for developing novel predictive, diagnostic, and prognostic biomarkers of preeclampsia to improve reproductive outcomes and reduce the risk for subsequent cardiovascular disease.

摘要

本研究旨在对正常妊娠胎盘和子痫前期胎盘的基因表达谱进行全面分析。胎盘组织在正常妊娠妇女(n=6)和子痫前期患者(n=6)分娩后立即获得。通过寡核苷酸 DNA 微阵列评估基因表达谱,并通过定量实时 RT-PCR 进行验证。通过 GeneSpring™ GX 11.0 软件和 Ingenuity Pathways Analysis(IPA)评估差异表达基因的功能关系和经典途径/网络。确定了 939 个表达差异显著的基因:与正常胎盘相比,子痫前期胎盘中 483 个基因上调,456 个基因下调(fold change ≥ 2,unpaired t-test 校正后 p<0.05)。IPA 显示这些基因的主要分子功能涉及细胞功能和维持、细胞发育、细胞信号转导和脂质代谢。通路分析表明,许多生物学通路,包括 Notch、Wnt、NF-κB 和转化生长因子-β(TGF-β)信号通路,在子痫前期发生异常调节。总之,我们的微阵列分析代表了胎盘基因表达谱和各种失调的信号通路的综合列表,这些通路在子痫前期中发生改变。这些观察结果可能为开发子痫前期的新型预测、诊断和预后生物标志物提供基础,以改善生殖结局并降低随后发生心血管疾病的风险。

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本文引用的文献

1
Differential gene expression analysis of placentas with increased vascular resistance and pre-eclampsia using whole-genome microarrays.使用全基因组微阵列对血管阻力增加的胎盘和子痫前期进行差异基因表达分析。
J Pregnancy. 2011;2011:472354. doi: 10.1155/2011/472354. Epub 2011 Mar 8.
2
Maternal insulin resistance and preeclampsia.母体胰岛素抵抗与子痫前期。
Am J Obstet Gynecol. 2011 Apr;204(4):327.e1-6. doi: 10.1016/j.ajog.2011.02.024.
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Preeclampsia leads to dysregulation of various signaling pathways in placenta.子痫前期导致胎盘内各种信号通路失调。
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Perfusion of human placenta with hemoglobin introduces preeclampsia-like injuries that are prevented by α1-microglobulin.用血红蛋白对人胎盘进行灌注会导致类似先兆子痫的损伤,而α1-微球蛋白可预防这种损伤。
Placenta. 2011 Apr;32(4):323-32. doi: 10.1016/j.placenta.2011.01.017. Epub 2011 Feb 26.
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Proteomic analysis reveals an elevated expression of heat shock protein 27 in preeclamptic placentas.蛋白质组学分析显示,子痫前期胎盘组织中热休克蛋白 27 表达升高。
Gynecol Obstet Invest. 2011;71(3):151-7. doi: 10.1159/000315162. Epub 2011 Feb 19.
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High mobility group box 1 (HMGB1) levels in the placenta and in serum in preeclampsia.子痫前期患者胎盘和血清中高迁移率族蛋白 B1(HMGB1)的水平。
Am J Reprod Immunol. 2011 Aug;66(2):143-8. doi: 10.1111/j.1600-0897.2010.00975.x. Epub 2011 Jan 18.
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Immunohistochemical expression of Annexin A5 in preeclamptic placentas.子痫前期胎盘组织中膜联蛋白 A5 的免疫组化表达。
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