Korean J Perinatol.  2008 Dec;19(4):341-350.

Analysis of gene expression in placenta of severe preeclampsia

• Lee GS
• Lee Y
• Yang DE
• Shin JC

Abstract

OBJECTIVE
This study was designed to detect genes specifically expressed in severe preeclamptic placentas.
METHODS
Placenta tissues were collected immediately after delivery from 5 preeclamptic patients and 5 normal pregnant women. Total RNAs of each placenta were extracted and hybridized for a cDNA microarray. Of the microarray data, four up-regulated genes (DSCR4, GPA, PCDHGB1, Hemogen) and four down-regulated genes (IL1R2, MGST1, GAS1 GREB1) were selected and reverse transcriptase-polymerase chain reaction was used to confirm the results of cDNA microarray.
RESULTS
The expression fold for each up-regulated gene was 2.2 times for DSCR4, 2.7 times for PCDHGB1, 3.5 times for Hemogen, 5.2 times for GPA on the cDNA microarray. The expression fold for each down-regulated gene was 3.3 times for IL1R2, 4.2 times for MGST1, 4.9 times for GAS1 and 2.3 times for GREB1 on the cDNA microarray. The expression fold for each up- regulated gene was 5.21 times for DSCR4, 3.01 times for PCDHGB1, and 4,53 times for Hemogen and 2.2 times for GPA on RT-PCR. The expression fold for each down-regulated gene was 2.7 times for IL1R2, 2.22 times for MGST1, 2.53 times for GAS1 and 1.83 times for GREB1 on the RT-PCR.
CONCLUSION
DSCR4, PCDHGB1, Hemogen and GPA as the up-regulated genes and IL1R2, MGST1, GAS1 and GREB1 as the down-regulated genes, which were found and selected by the cDNA microarray, might be considered to be novel biomarkers for preeclampsia.

Keyword

Preeclampsia; Placenta; Microarray analysis

MeSH Terms

Biomarkers
Chimera
Female
Gene Expression
Humans
Microarray Analysis
Oligonucleotide Array Sequence Analysis
Placenta
Pre-Eclampsia
Pregnant Women
RNA
RNA