Evidence map›Paper›PMID 26457081›Full record

ArticleInternational journal of endocrinology2015

Methylation of the Corticotropin Releasing Hormone Gene Promoter in BeWo Cells: Relationship to Gene Activity.

Xin Pan, Maria Bowman, Rodney J Scott, John Fitter, Richard C Nicholson, Roger Smith, Tamas Zakar

Open access · goldAbstract read
In one paragraph

Article in International journal of endocrinology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
4.0field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 10 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

Xin PanMothers and Babies Research Centre, Hunter Medical Research Institute, New Lambton Heights, NSW 2305, Australia ; Faculty of Health and Medicine, University of Newcastle, Callaghan, NSW 2308, Australia ; Department of Obstetrics and Gynaecology, Second Affiliated Hospital, Chongqing Medical University, Chongqing, China.
Maria BowmanMothers and Babies Research Centre, Hunter Medical Research Institute, New Lambton Heights, NSW 2305, Australia.
Rodney J ScottMothers and Babies Research Centre, Hunter Medical Research Institute, New Lambton Heights, NSW 2305, Australia ; Faculty of Health and Medicine, University of Newcastle, Callaghan, NSW 2308, Australia ; Molecular Medicine, Hunter Area Pathology Service, New Lambton Heights, NSW 2310, Australia.
John FitterMothers and Babies Research Centre, Hunter Medical Research Institute, New Lambton Heights, NSW 2305, Australia ; Faculty of Health and Medicine, University of Newcastle, Callaghan, NSW 2308, Australia.
Richard C NicholsonMothers and Babies Research Centre, Hunter Medical Research Institute, New Lambton Heights, NSW 2305, Australia ; John Hunter Hospital, New Lambton Heights, NSW 2310, Australia.
Roger SmithMothers and Babies Research Centre, Hunter Medical Research Institute, New Lambton Heights, NSW 2305, Australia ; Faculty of Health and Medicine, University of Newcastle, Callaghan, NSW 2308, Australia ; John Hunter Hospital, New Lambton Heights, NSW 2310, Australia.
Tamas ZakarMothers and Babies Research Centre, Hunter Medical Research Institute, New Lambton Heights, NSW 2305, Australia ; Faculty of Health and Medicine, University of Newcastle, Callaghan, NSW 2308, Australia ; John Hunter Hospital, New Lambton Heights, NSW 2310, Australia.
Hunter Medical Research Institute · AUJohn Hunter Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Corticotropin releasing hormone (CRH) production by the human placenta increases exponentially as pregnancy advances, and the rate of increase predicts gestational length. CRH gene expression is regulated by cAMP in trophoblasts through a cyclic AMP-response element (CRE), which changes its transcription factor binding properties upon methylation. Here we determined whether methylation of the CRH proximal promoter controls basal and cAMP-stimulated CRH expression in BeWo cells, a well-characterized trophoblastic cell line. We treated the cells with 8-Br-cAMP and the DNA methyltransferase inhibitor 5-aza-2' deoxycytidine (5-AZA-dC) and determined the effects on CRH mRNA level and promoter methylation. Clonal bisulfite sequencing showed partial and allele independent methylation of CpGs in the CRH promoter. CRH mRNA expression and the methylation of a subset of CpGs (including CpG2 in the CRE) increased spontaneously during culture. 8-Br-cAMP stimulated CRH expression without affecting the increase in methylation. 5-AZA-dC decreased methylation and augmented 8-Br-cAMP-stimulated CRH expression, but it blocked the spontaneous increase of CRH mRNA level. We conclude that the CRH promoter is a dynamically and intermediately methylated genomic region in BeWo cells. Promoter methylation did not inhibit CRH gene expression under the conditions employed; rather it determined the contribution of alternative cAMP-independent pathways and cAMP-independent mechanisms to CRH expression control.

Identifiers

PMID26457081
PMCPMC4589633
OpenAlexW1851128041

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.