Literature DB >> 19886237

Expression of caspase-3, Bax nad Bcl-2 in placentas from pregnancies complicated by treated and non-treated fetal growth restriction.

Karowicz-Bilińska Agata1, Szczerba Anita, Kowalska-Koprek Urszula, Nawrocka-Kunecka Agnieszka, Bartosz Grzegorz.   

Abstract

BACKGROUND: Fetal growth restriction (FGR) is the reason of high prematurity rate and its later complications. Restriction of utero-placental circulation, which could be changed by IURG treatment, plays the main role in FGR. The results of changes in apoptosis-related genes expression due to FGR treatment may help further in the prevention and treatment of FGR.
MATERIAL AND METHODS: Caspase-3, Bax and Bcl-2 expressions in normal pregnancies and those complicated by treated and untreated FGR have been compared. The study was conducted in 2005-2006 at the High-Risk Pregnancy Unit of Medical University in Łódź and Kopernik Hospital in Łódź. Caspase-3, Bax and Bcl-2 expressions were assessed by immunohistochemical method Bcl-2 was assessed in the trophoblast, Bax and caspase-3 in the decidua and the trophoblast.
RESULTS: The mean value of Bcl-2 in the trophoblast was 58.8 +/- 12.7 in the FGR-untreated group, 37.0 +/- 0.5 in the FGR-treated group and 65.7 +/- 6.9 in the control group. In the FGR-untreated group the mean value of Bax expression was 60.6 +/- 10.7 in the trophoblast and 32.0 +/- 7.3 in the decidua. In the FGR-treated group the mean value of Bax expression was 42.2 +/- 12.2 in the trophoblast and 20.9 +/- 6.4 in the decidua. In the control group the mean value of Bax expression was 13.6 +/- 2.2 in the trophoblast and 6.6 +/- 6.8 in the decidua. In the FGR-untreated group the mean value of Cpp-32 expression was 40.1 +/- 9.1 in the trophoblast and 42.6 +/- 12.5 in the decidua. In the FGR-treated group the mean value of Cpp-32 expression was 21.3 +/- 6.8 in the trophoblast and 23.7 +/- 5.1 in the decidua. In the control group the mean value of Cpp-32 expression was 13.6 +/- 6.3 in trophoblast and 11.6 +/- 5.3 in the decidua.
CONCLUSIONS: Increased expression of pro-apoptotic proteins in the placenta might be one of the reasons for FGR development. The treatment used in the FGR group decreased the process of apoptosis.

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Year:  2009        PMID: 19886237

Source DB:  PubMed          Journal:  Ginekol Pol        ISSN: 0017-0011            Impact factor:   1.232


  2 in total

1.  An EG-VEGF-Dependent Decrease in Homeobox Gene NKX3.1 Contributes to Cytotrophoblast Dysfunction: A Possible Mechanism in Human Fetal Growth Restriction.

Authors:  Padma Murthi; Sophie Brouillet; Anita Pratt; Anthony Borg; Bill Kalionis; Frederic Goffin; Vassilis Tsatsaris; Carine Munaut; Jean-Jacques Feige; Mohamed Benharouga; Thierry Fournier; Nadia Alfaidy
Journal:  Mol Med       Date:  2015-07-21       Impact factor: 6.354

2.  Expression of the placental transcriptome in maternal nutrient reduction in baboons is dependent on fetal sex.

Authors:  Laura A Cox; Cun Li; Jeremy P Glenn; Kenneth Lange; Kimberly D Spradling; Peter W Nathanielsz; Thomas Jansson
Journal:  J Nutr       Date:  2013-09-18       Impact factor: 4.798

  2 in total

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