Placental microRNA expression in pregnancies complicated by preeclampsia

被引:257
作者
Enquobahrie, Daniel A. [1 ,2 ,3 ]
Abetew, Dejene F. [1 ]
Sorensen, Tanya K. [1 ]
Willoughby, David [4 ]
Chidambaram, Kumaravel [4 ]
Williams, Michelle A. [1 ,3 ]
机构
[1] Univ Washington, Ctr Perinatal Studies, Swedish Med Ctr, Seattle, WA 98104 USA
[2] Univ Washington, Cardiovasc Hlth Res Unit, Seattle, WA 98104 USA
[3] Univ Washington, Dept Epidemiol, Seattle, WA 98104 USA
[4] Oceanridge Biosci, Palm Beach Gardens, FL USA
基金
美国国家卫生研究院;
关键词
expression; microRNA; placenta; preeclampsia; GROWTH-FACTOR-I; GENE-EXPRESSION; RECEPTOR; HYPOXIA; CLUSTER; WOMEN;
D O I
10.1016/j.ajog.2010.09.004
中图分类号
R71 [妇产科学];
学科分类号
100211 [妇产科学];
摘要
OBJECTIVE: The role of posttranscription regulation in preeclampsia is largely unknown. We investigated preeclampsia-related placental microRNA (miRNA) expression using microarray and confirmatory quantitative real-time polymerase chain reaction experiments. STUDY DESIGN: Placental expressions of characterized and novel miRNAs (1295 probes) were measured in samples collected from 20 preeclampsia cases and 20 controls. Differential expression was evaluated using Student t test and fold change analyses. In pathway analysis, we examined functions/functional relationships of targets of differentially expressed miRNAs. RESULTS: Eight miRNAs were differentially expressed (1 up-regulated and 7 down-regulated) among preeclampsia cases compared with controls. These included previously identified candidates (miR-210, miR-1, and a miRNA in the 14q32.31 cluster region) and others that are novel (miR-584 and miR-34c-5p). These miRNAs target genes that participate in organ/system development (cardiovascular and reproductive system), immunologic dysfunction, cell adhesion, cell cycle, and signaling. CONCLUSION: Expression of miRNAs that target genes in diverse pathophysiological processes is altered in the setting of preeclampsia.
引用
收藏
页码:178.e12 / 178.e21
页数:10
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