Evidence map›Paper›PMID 22880087›Full record

ArticlePloS one2012

Aberrant promoter methylation and expression of UTF1 during cervical carcinogenesis.

Samuel Guenin, Mustapha Mouallif, Rachel Deplus, Xavier Lampe, Nathalie Krusy, Emilie Calonne, Katty Delbecque, Frederic Kridelka, François Fuks, My Mustapha Ennaji and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

20 citing papers in PubMed, 27 citations in OpenAlex.

  1. Epigenetics · 2024
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  5. AQP5-1364A/C Polymorphism AffectsInternational journal of molecular sciences · 2022
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  11. Identification ofFrontiers in genetics · 2018
    Article
  12. Article
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  15. Cervical cancer stem cells: opportunities and challenges.Journal of cancer research and clinical oncology · 2015
    Review
  16. Article
  17. Article
  18. Embryonic stem cell-specific signature in cervical cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Review
  19. Article
  20. Analysis of the methylation patterns of the p16 INK4A, p15 INK4B, and APC genes in gastric adenocarcinoma patients from a Brazilian population.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2013
    Article
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

11 authors at 3 institutions in 2 countries.

Samuel GueninLaboratory of Experimental Pathology, Groupe Interdisciplinaire de Génoprotéomique Appliquée-Cancer, University of Liège, Liège, Belgium. samuel.guenin@gmail.com
Mustapha Mouallif
Rachel Deplus
Xavier Lampe
Nathalie Krusy
Emilie Calonne
Katty Delbecque
Frederic Kridelka
François Fuks
My Mustapha Ennaji
Philippe Delvenne
University of Liège · BECentre Hospitalier Universitaire de Liège · BEUniversité Hassan II Mohammedia · MA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Promoter methylation profiles are proposed as potential prognosis and/or diagnosis biomarkers in cervical cancer. Up to now, little is known about the promoter methylation profile and expression pattern of stem cell (SC) markers during tumor development. In this study, we were interested to identify SC genes methylation profiles during cervical carcinogenesis. A genome-wide promoter methylation screening revealed a strong hypermethylation of Undifferentiated cell Transcription Factor 1 (UTF1) promoter in cervical cancer in comparison with normal ectocervix. By direct bisulfite pyrosequencing of DNA isolated from liquid-based cytological samples, we showed that UTF1 promoter methylation increases with lesion severity, the highest level of methylation being found in carcinoma. This hypermethylation was associated with increased UTF1 mRNA and protein expression. By using quantitative RT-PCR and Western Blot, we showed that both UTF1 mRNA and protein are present in epithelial cancer cell lines, even in the absence of its two main described regulators Oct4A and Sox2. Moreover, by immunofluorescence, we confirmed the nuclear localisation of UTF1 in cell lines. Surprisingly, direct bisulfite pyrosequencing revealed that the inhibition of DNA methyltransferase by 5-aza-2'-deoxycytidine was associated with decreased UTF1 gene methylation and expression in two cervical cancer cell lines of the four tested. These findings strongly suggest that UTF1 promoter methylation profile might be a useful biomarker for cervical cancer diagnosis and raise the questions of its role during epithelial carcinogenesis and of the mechanisms regulating its expression.

Indexed as

Gene Expression Regulation, NeoplasticPromoter Regions, GeneticAzacitidineCarcinoma, Ovarian EpithelialCell Line, TumorCell ProliferationCell SurvivalCell Transformation, NeoplasticCervix UteriCluster AnalysisCytological TechniquesDNA MethylationDNA, NeoplasmFemaleGenes, NeoplasmHumansAzacitidineDNA, NeoplasmNuclear ProteinsOctamer Transcription Factor-3POU5F1 protein, humanSOX2 protein, humanSOXB1 Transcription FactorsTrans-ActivatorsUTF1 protein, human

Identifiers

PMID22880087
PMCPMC3411846
OpenAlexW2098840211

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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.