Evidence map›Paper›PMID 29576538›Full record

ArticleStem cell reports2018

A Critical Role of TET1/2 Proteins in Cell-Cycle Progression of Trophoblast Stem Cells.

Stephanie Chrysanthou, Claire E Senner, Laura Woods, Elena Fineberg, Hanneke Okkenhaug, Sarah Burge, Vicente Perez-Garcia, Myriam Hemberger

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

31 citing papers in PubMed, 49 citations in OpenAlex.

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  12. Cells · 2022
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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

8 authors at 2 institutions in 1 country.

Stephanie ChrysanthouEpigenetics Programme, The Babraham Institute, Babraham Research Campus, Cambridge CB22 3AT, UK; Centre for Trophoblast Research, University of Cambridge, Downing Street, Cambridge CB2 3EG, UK.
Claire E SennerEpigenetics Programme, The Babraham Institute, Babraham Research Campus, Cambridge CB22 3AT, UK; Centre for Trophoblast Research, University of Cambridge, Downing Street, Cambridge CB2 3EG, UK.
Laura WoodsEpigenetics Programme, The Babraham Institute, Babraham Research Campus, Cambridge CB22 3AT, UK; Centre for Trophoblast Research, University of Cambridge, Downing Street, Cambridge CB2 3EG, UK.
Elena FinebergEpigenetics Programme, The Babraham Institute, Babraham Research Campus, Cambridge CB22 3AT, UK; Centre for Trophoblast Research, University of Cambridge, Downing Street, Cambridge CB2 3EG, UK.
Hanneke OkkenhaugImaging Facility, The Babraham Institute, Babraham Research Campus, Cambridge CB22 3AT, UK.
Sarah BurgeEpigenetics Programme, The Babraham Institute, Babraham Research Campus, Cambridge CB22 3AT, UK.
Vicente Perez-GarciaEpigenetics Programme, The Babraham Institute, Babraham Research Campus, Cambridge CB22 3AT, UK; Centre for Trophoblast Research, University of Cambridge, Downing Street, Cambridge CB2 3EG, UK.
Myriam HembergerEpigenetics Programme, The Babraham Institute, Babraham Research Campus, Cambridge CB22 3AT, UK; Centre for Trophoblast Research, University of Cambridge, Downing Street, Cambridge CB2 3EG, UK. Electronic address: myriam.hemberger@babraham.ac.uk.
Babraham Institute · GBUniversity of Cambridge · GB

Funding

Biotechnology and Biological Sciences Research Council BBS/E/B/000C0400Biotechnology and Biological Sciences Research Council BBS/E/B/000C0403Biotechnology and Biological Sciences Research Council BBS/E/B/000C0421Medical Research Council 1425742
6 · The paper itself

Abstract

The ten-eleven translocation (TET) proteins are well known for their role in maintaining naive pluripotency of embryonic stem cells. Here, we demonstrate that, jointly, TET1 and TET2 also safeguard the self-renewal potential of trophoblast stem cells (TSCs) and have partially redundant roles in maintaining the epithelial integrity of TSCs. For the more abundantly expressed TET1, we show that this is achieved by binding to critical epithelial genes, notably E-cadherin, which becomes hyper-methylated and downregulated in the absence of TET1. The epithelial-to-mesenchymal transition phenotype of mutant TSCs is accompanied by centrosome duplication and separation defects. Moreover, we identify a role of TET1 in maintaining cyclin B1 stability, thereby acting as facilitator of mitotic cell-cycle progression. As a result, Tet1/2 mutant TSCs are prone to undergo endoreduplicative cell cycles leading to the formation of polyploid trophoblast giant cells. Taken together, our data reveal essential functions of TET proteins in the trophoblast lineage.

Indexed as

Cell CycleAnimalsCell LineCell Nucleus ShapeCentrosomeCyclin B1EndoreduplicationEpithelial CellsEpithelial-Mesenchymal TransitionGene Expression RegulationGene Knockout TechniquesHumansPolyploidyProtein StabilityProto-Oncogene ProteinsStem CellsCyclin B1Proto-Oncogene Proteinscell cycledifferentiationendoreduplicationmitosisself-renewalTET proteinstrophoblast giant cellstrophoblast stem cells

Identifiers

PMID29576538
PMCPMC5998911
OpenAlexW2789621687

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.