Analysis of the Placental Tissue Transcriptome of Normal and Preeclampsia Complicated Pregnancies

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Abstract

Preeclampsia is one of the most severe gestational complications which is one of the leading causes of maternal and perinatal morbidity and mortality. A growth in the incidence of severe and combined forms of the pathology has been observed in recent years. According to modern concepts, inadequate cytotrophoblast invasion into the spiral arteries of the uterus and development of the ischemia-reperfusion syndrome in the placental tissue play the leading role in the development of preeclampsia, which is characterized by multipleorgan failure. In this regard, our work was aimed at studying the patterns of placental tissue transcriptome that are specific to females with PE and with physiological pregnancy, as well as identifying the potential promising biomarkers and molecular mechanisms of this pathology. We have identified 63 genes whose expression proved to differ significantly in the placental tissue of females with PE and with physiological pregnancy. A cluster of differentially expressed genes (DEG) whose expression level is increased in patients with preeclampsia includes not only the known candidate genes that have been identified in many other genome-wide studies (e.g., LEP, BHLHB2, SIGLEC6, RDH13, BCL6), but also new genes (ANKRD37, SYDE1, CYBA, ITGB2, etc.), which can be considered as new biological markers of preeclampsia and are of further interest. The results of a functional annotation of DEG show that the development of preeclampsia may be related to a stress response, immune processes, the regulation of cell-cell interactions, intracellular signaling cascades, etc. In addition, the features of the differential gene expression depending on preeclampsia severity were revealed. We have found evidence of the important role of the molecular mechanisms responsible for the failure of immunological tolerance and initiation of the pro-inflammatory cascade in the development of severe preeclampsia. The results obtained elaborate the concept of the pathophysiology of preeclampsia and contain the information necessary to work out measures for targeted therapy of this disease.

About the authors

E. A. Trifonova

Research Institute of Medical Genetics, Siberian Branch, Russian Academy of Medical Sciences; Tomsk State University

Author for correspondence.
Email: vadim.stepanov@medgenetics.ru
Russian Federation

T. V. Gabidulina

Siberian State Medical University, Ministry of Health of the Russian Federation

Email: vadim.stepanov@medgenetics.ru
Russian Federation

N. I. Ershov

Institute of Cytology and Genetics, Siberian Branch, Russian Academy of Sciences

Email: vadim.stepanov@medgenetics.ru
Russian Federation

V. N. Serebrova

Research Institute of Medical Genetics, Siberian Branch, Russian Academy of Medical Sciences

Email: vadim.stepanov@medgenetics.ru
Russian Federation

A. Yu. Vorozhishcheva

City Clinical Hospital № 1

Email: vadim.stepanov@medgenetics.ru
Russian Federation

V. A. Stepanov

Research Institute of Medical Genetics, Siberian Branch, Russian Academy of Medical Sciences; Tomsk State University

Email: vadim.stepanov@medgenetics.ru
Russian Federation

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Copyright (c) 2014 Trifonova E.A., Gabidulina T.V., Ershov N.I., Serebrova V.N., Vorozhishcheva A.Y., Stepanov V.A.

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