Pineles Beth L, Romero Roberto, Montenegro Daniel, Tarca Adi L, Han Yu Mi, Kim Yeon Mee, Draghici Sorin, Espinoza Jimmy, Kusanovic Juan Pedro, Mittal Pooja, Hassan Sonia S, Kim Chong Jai
Perinatology Research Branch, National Institute of Child Health and Human Development/National Institutes of Health/Department of Health and Human Services, Bethesda, MD, USA.
Am J Obstet Gynecol. 2007 Mar;196(3):261.e1-6. doi: 10.1016/j.ajog.2007.01.008.
Preeclampsia and small-for-gestational age (SGA) neonates have partially overlapping clinicopathologic features. MicroRNAs (miRNAs) are critical posttranscriptional regulators of gene expression. This study was performed to determine whether preeclampsia and SGA are associated with alterations in placental miRNA expression.
Placentas were obtained from patients with (1) preeclampsia (n = 9); (2) SGA (n = 9); (3) preeclampsia + SGA (n = 9); and (4) a control group with spontaneous preterm labor and delivery (PTL; n = 9). The expression of 157 miRNAs was assessed by real-time quantitative reverse transcription-polymerase chain reaction.
Differential expression between preeclampsia and the control group (miR-210, miR-182) and between preeclampsia + SGA and the control group (miR-210, miR-182*, and others) was found. Gene Ontology analysis of the target genes revealed enrichment for specific biological process categories (antiapoptosis: miR-182; regulation of transcription: miR-210).
This study reports, for the first time, increased expression of specific placental miRNAs in preeclampsia with and without SGA. The findings also provide novel targets for further investigation of the pathophysiology of preeclampsia.
子痫前期和小于胎龄(SGA)新生儿具有部分重叠的临床病理特征。微小RNA(miRNA)是基因表达关键的转录后调节因子。本研究旨在确定子痫前期和SGA是否与胎盘miRNA表达改变有关。
胎盘取自以下患者:(1)子痫前期(n = 9);(2)SGA(n = 9);(3)子痫前期+SGA(n = 9);以及(4)自然早产分娩(PTL)对照组(n = 9)。通过实时定量逆转录-聚合酶链反应评估157种miRNA的表达。
发现子痫前期与对照组之间(miR-210、miR-182)以及子痫前期+SGA与对照组之间(miR-210、miR-182*等)存在差异表达。对靶基因的基因本体分析显示特定生物学过程类别富集(抗凋亡:miR-182;转录调控:miR-210)。
本研究首次报道了无论有无SGA,子痫前期胎盘特定miRNA表达增加。这些发现也为子痫前期病理生理学的进一步研究提供了新的靶点。