Department of Obstetrics, The First Affiliated Hospital of China Medical University, Shenyang, People's Republic of China.
OMICS. 2012 Jun;16(6):301-11. doi: 10.1089/omi.2011.0066.
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.
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。