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miRNAs as Common Regulators of the Transforming Growth Factor (TGF)-β Pathway in the Preeclamptic Placenta and Cadmium-treated Trophoblasts: Links between the Environment the Epigenome and Preeclampsia

机译:miRNA作为子痫前期胎盘和镉处理的滋养细胞中转化生长因子(TGF)-β途径的常见调节剂:环境表观基因组和子痫前期之间的联系

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摘要

Preeclampsia (PE) is a pregnancy disorder characterized by high blood pressure and proteinuria that can cause adverse health effects in both mother and fetus. There is no current cure for PE other than delivery of the fetus. While the etiology is unknown, poor placentation of the placenta due to aberrant signaling of growth and angiogenic factors has been postulated as causal factors of PE. In addition, environmental contaminants, such as the metal cadmium (Cd), have been linked to placental toxicity and increased risk of developing PE. Here, we use a translational study design to investigate genomic and epigenomic alterations in both placentas and placental trophoblasts, focused on the angiogenesis-associated transforming growth factor-beta (TGF-β) pathway. Genes within the TGF-β pathway displayed increased expression in both the preeclamptic placenta and Cd-treated trophoblasts. In addition, miRNAs that target the TGF-β pathway were also significantly altered within the preeclamptic placenta and Cd-treated trophoblasts. Integrative analysis resulted in the identification of a subset of Cd-responsive miRNAs, including miR-26a and miR-155, common to preeclamptic placentas and Cd-treated trophoblasts. These miRNAs have previously been linked to PE and are predicted to regulate members of the TGF-β pathway. Results from this study provide future targets for PE treatment.
机译:子痫前期(PE)是一种妊娠高血压疾病,其特征在于高血压和蛋白尿,可对母亲和胎儿造成不利的健康影响。目前,除了分娩胎儿外,目前还没有其他治疗PE的方法。尽管病因不明,但由于生长异常信号和血管生成因子引起的胎盘胎盘发育不良是PE的致病因素。另外,环境污染物,例如金属镉(Cd),与胎盘毒性和发展为PE的风险增加有关。在这里,我们使用转化研究设计来研究胎盘和胎盘滋养细胞的基因组和表观基因组变化,重点是与血管新生相关的转化生长因子-β(TGF-β)途径。 TGF-β途径内的基因在先兆子痫胎盘和Cd处理的滋养细胞中均显示出增加的表达。此外,靶向TGF-β途径的miRNA在先兆子痫胎盘和Cd处理的滋养细胞中也发生了显着变化。整合分析导致鉴定了子痫前胎盘和Cd处理过的滋养细胞常见的Cd反应性miRNA子集,包括miR-26a和miR-155。这些miRNA先前已与PE连接,并被预测可调节TGF-β途径的成员。这项研究的结果为PE治疗提供了未来的目标。

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