Evidence map›Paper›PMID 34571856›Full record

ArticleCells2021

DNA Methylation of TGFβ Target Genes: Epigenetic Control of TGFβ Functional Duality in Liver Cancer.

Kevin Bévant, Matthis Desoteux, Abdel Hady A Abdel Wahab, Sabrin A Abdel Wahab, Ayman Mohamed Metwally, Cédric Coulouarn

Open access · goldAbstract read
In one paragraph

Article in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. The Mechanism of DNA Methylation and miRNA in Breast Cancer.International journal of molecular sciences · 2023
    Review
  8. Article
  9. Review
  10. Review
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

6 authors at 3 institutions in 2 countries.

Kevin BévantCentre de Lutte Contre le Cancer Eugène Marquis, Inserm, University of Rennes 1, UMR_S 1242, COSS (Chemistry, Oncogenesis Stress Signaling), 35042 Rennes, France.ORCID 0000-0002-4136-6936
Matthis DesoteuxCentre de Lutte Contre le Cancer Eugène Marquis, Inserm, University of Rennes 1, UMR_S 1242, COSS (Chemistry, Oncogenesis Stress Signaling), 35042 Rennes, France.ORCID 0000-0002-3412-2730
Abdel Hady A Abdel WahabDepartment of Cancer Biology, National Cancer Institute, Cairo University, Cairo 11796, Egypt.
Sabrin A Abdel WahabMedical Laboratory Department, Students Hospital, Cairo University, Cairo 11796, Egypt.
Ayman Mohamed MetwallyMedical Laboratory Technology Department, College of Applied Health Science Technology, Misr University for Science and Technology (MUST), Al-Motamayez District, 6th of October P.O. Box 77, Egypt.
Cédric CoulouarnCentre de Lutte Contre le Cancer Eugène Marquis, Inserm, University of Rennes 1, UMR_S 1242, COSS (Chemistry, Oncogenesis Stress Signaling), 35042 Rennes, France.ORCID 0000-0002-5692-9586
Inserm · FRCairo University · EGMisr University for Science and Technology · EG

Funding

Campus France in the framework of the Franco-Egyptian partnership IMHOTEP Hubert Curien program between Univ Rennes 1, Inserm and Faculty of Applied Medical Sciences Misr University for Science for science and technology project N° 39530VDINCa, and ITMO Cancer AVIESAN (Alliance Nationale pour les Sciences de la Vie et de la Santé) dans le cadre du Plan cancer (Non-coding RNA in cancerology: fundamental to translational) Plan cancerInserm, Université de Rennes 1, Ligue Contre le Cancer (CD22, CD35, CD85) recurrent fundingLigue Contre le Cancer (CD22) and Région Bretagne PhD fellowship
6 · The paper itself

Abstract

Transforming growth factor beta (TGFβ) plays a key role in liver carcinogenesis. However, its action is complex, since TGFβ exhibits tumor-suppressive or oncogenic properties, depending on the tumor stage. At an early stage TGFβ exhibits cytostatic features, but at a later stage it promotes cell growth and metastasis, as a potent inducer of epithelial to mesenchymal transition (EMT). Here, we evaluated DNA methylation as a possible molecular mechanism switching TGFβ activity toward tumor progression in hepatocellular carcinoma (HCC). We report that decitabine, a demethylating agent already used in the clinic for the treatment of several cancers, greatly impairs the transcriptional response of SNU449 HCC cells to TGFβ. Importantly, decitabine was shown to induce the expression of EMT-related transcription factors (e.g.,

Indexed as

Carcinoma, HepatocellularCell Line, TumorCell MovementCell ProliferationCell Transformation, NeoplasticDecitabineDNA MethylationEpigenesis, GeneticEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHumansLiverLiver NeoplasmsNeoplasm Recurrence, LocalSignal TransductionSnail Family Transcription FactorsDecitabineSNAI1 protein, humanSnail Family Transcription FactorsTranscription FactorsTransforming Growth Factor betaDNA methylationEMTepigeneticshepatocellular carcinomaTGFβ

Identifiers

PMID34571856
PMCPMC8468746
OpenAlexW3197514590

What OpenQuestion holds

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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.