Targeted gene analysis: increased B-cell lymphoma 6 in preeclamptic placentas.

Abstract:

:Preeclampsia is a leading cause for maternal and perinatal mortality and morbidity. Microarray-based transcriptional profiling has been widely used for identifying genes responsible for preeclampsia. These studies deliver multiple pictures of gene signatures, implying the complicated pathophysiology. In the present work, we designed our own gene array containing genes involved in various signaling transduction pathways and analyzed placental samples from patients with preeclampsia and controls. We verify that genes associated with angiogenesis and migration pathways are mostly altered in preeclamptic placentas. Interestingly, several genes including B-cell lymphoma 6 have been identified to be linked to preeclampsia. Increased expression of B-cell lymphoma 6 is correlated with enhanced FLT1 and LEPTIN, the hallmarks of preeclampsia. Moreover, the protein level of B-cell lymphoma 6 is elevated in preeclamptic placentas and is predominantly localized in the nucleus of villous cytotrophoblasts lying directly underneath the syncytial layer, suggestive of an involvement in the function of villous trophoblasts. Altered B-cell lymphoma 6, a key oncogene in B-cell lymphomagenesis, may be involved in the pathogenesis of preeclampsia, and further investigations are required to decipher the molecular mechanisms.

journal_name

Hum Pathol

journal_title

Human pathology

authors

Louwen F,Muschol-Steinmetz C,Friemel A,Kämpf AK,Töttel E,Reinhard J,Yuan J

doi

10.1016/j.humpath.2014.02.002

subject

Has Abstract

pub_date

2014-06-01 00:00:00

pages

1234-42

issue

6

eissn

0046-8177

issn

1532-8392

pii

S0046-8177(14)00066-5

journal_volume

45

pub_type

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