Activin signalling and pre-eclampsia: From genetic risk to pre-symptomatic biomarker
•Pre-eclampsia is a leading cause of maternal and fetal mortality.•Activin A serum and placental levels are increased in cases of pre-eclampsia.•Activin A is therefore being examined as a biomarker for pre-eclampsia. Pre-eclampsia is a multi-system condition in pregnancy that is characterised by the...
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Veröffentlicht in: | Cytokine (Philadelphia, Pa.) Pa.), 2015-02, Vol.71 (2), p.360-365 |
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Sprache: | eng |
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Zusammenfassung: | •Pre-eclampsia is a leading cause of maternal and fetal mortality.•Activin A serum and placental levels are increased in cases of pre-eclampsia.•Activin A is therefore being examined as a biomarker for pre-eclampsia.
Pre-eclampsia is a multi-system condition in pregnancy that is characterised by the onset of hypertension and proteinuria in women after the 20th week and it remains a leading cause of maternal and fetal mortality. Despite this the causative molecular basis of pre-eclampsia remains poorly understood. As a result, an intensive research effort has focused on understanding the molecular mechanisms involved in pre-eclampsia and using this information to identify new pre-symptomatic bio-markers of the condition. Activin A and its receptor, ACVR2A, have been extensively studied in this regard.
Activin A is a member of the transforming growth factor (TGF)-β superfamily that has a wide range of biological functions depending on the cellular context. Recent work has shown that polymorphisms in ACVR2A may be a genetic risk factor for pre-eclampsia. Furthermore, both placenta and serum levels of Activin A are significantly increased in pre-eclampsia suggesting that Activin A may be a possible biomarker for the condition. Here we review the latest advances in this field and link these with new molecular data that suggest that the oxidative stress and pro-inflammatory cytokine production seen in pre-eclampsia may result in increased placental Activin A secretion in an attempt to maintain placental function. |
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ISSN: | 1043-4666 1096-0023 |
DOI: | 10.1016/j.cyto.2014.11.017 |