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Vol. 62, No. 2, 2006   

Free Abstract     Article (References)     Article (PDF 257 KB)     

Free Tables S1-S2-S3 (2 MB)

Original Article

Genomewide Oligonucleotide Microarray Analysis on Placentae of Pre-Eclamptic Pregnancies
Rongrong Zhoua, Qianyong Zhuc, d, Yahui Wangc, Yonghong Renc, Liang Zhangc, Yuxiang Zhoua-c

aDepartment of Biological Sciences and Biotechnology, and
bSchool of Medicine, Tsinghua University, Beijing,
cNational Engineering Research Center for Beijing Biochip Technology, Beijing, and
dThe Third Military Medical University, Chongqing, PR China

Address of Corresponding Author

Gynecol Obstet Invest 2006;62:108-114 (DOI: 10.1159/000092857)


 goto top of page Key Words

  • DNA microarrays
  • Placenta
  • Pre-eclampsia

 goto top of page Abstract

Objective: Human placentae from normal and pre-eclamptic pregnancies were evaluated for possible changes in gene expression by microarray analysis to uncover new clues for the research of the etiology of pre-eclampsia. Methods: Placentae from five normal pregnancies and five pregnancies complicated by pre-eclampsia were collected. mRNA levels of five pre-eclamptic placentae were examined using genome-wide 70-mer oligonucleotide microarrays (CapitalBio, Beijing, China) in comparison with the pooled control consisting of total RNA from five normotensive placentae. Results: Ninety-six genes were found consistently down- or up-regulated in at least four pre-eclamptic samples. Most of them were related to an imbalance of reactive oxygen metabolites in placenta, abnormal trophoblast invasion, disorders of lipoprotein metabolism and signal transduction, or some that have been reported to have close correlation to the pathology of pre-eclampsia. The microarray data were also confirmed by the measurement of real-time PCR. Conclusion: DNA microarray is a high throughput and time-saving method to monitor altered gene expression. The results could provide interesting clues to the etiology of pre-eclampsia and lead to further studies in a more targeted fashion.

Copyright © 2006 S. Karger AG, Basel


 goto top of page Author Contacts

Yuxiang Zhou, MD
Department of Biological Science and Biotechnology
Tsinghua University
Beijing, 100084 (China)
Tel./Fax +86 10 8072 6858, E-Mail zhougyx@mail.tsinghua.edu.cn


 goto top of page Article Information

Received: May 10, 2005
Accepted after revision: January 2, 2006
Published online: April 25, 2006
Number of Print Pages : 7
Number of Figures : 3, Number of Tables : 5, Number of References : 27

 
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