Evidence map›Paper›PMID 25101295›Full record

ArticleBioMed research international2014

Identification of a novel methylated gene in nasopharyngeal carcinoma: TTC40.

Wajdi Ayadi, Nesrine Allaya, Hanèn Frikha, Emna Trigui, Abdelmajid Khabir, Abdelmonem Ghorbel, Jamel Daoud, Mounir Frikha, Ali Gargouri, Raja Mokdad-Gargouri

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

3 citing papers in PubMed, 6 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

10 authors at 2 institutions in 1 country.

Wajdi AyadiLaboratory of Biomass Valorization and Protein Production in Eukaryotes, Center of Biotechnology of Sfax, University of Sfax, 3038 Sfax, Tunisia.
Nesrine AllayaLaboratory of Biomass Valorization and Protein Production in Eukaryotes, Center of Biotechnology of Sfax, University of Sfax, 3038 Sfax, Tunisia.
Hanèn FrikhaLaboratory of Biomass Valorization and Protein Production in Eukaryotes, Center of Biotechnology of Sfax, University of Sfax, 3038 Sfax, Tunisia.
Emna TriguiLaboratory of Biomass Valorization and Protein Production in Eukaryotes, Center of Biotechnology of Sfax, University of Sfax, 3038 Sfax, Tunisia.
Abdelmajid KhabirUniversity Hospital Habib Bourguiba of Sfax, 3029 Sfax, Tunisia.
Abdelmonem GhorbelUniversity Hospital Habib Bourguiba of Sfax, 3029 Sfax, Tunisia.
Jamel DaoudUniversity Hospital Habib Bourguiba of Sfax, 3029 Sfax, Tunisia.
Mounir FrikhaUniversity Hospital Habib Bourguiba of Sfax, 3029 Sfax, Tunisia.
Ali GargouriLaboratory of Biomass Valorization and Protein Production in Eukaryotes, Center of Biotechnology of Sfax, University of Sfax, 3038 Sfax, Tunisia.ORCID 0000-0001-5009-9000
Raja Mokdad-GargouriLaboratory of Biomass Valorization and Protein Production in Eukaryotes, Center of Biotechnology of Sfax, University of Sfax, 3038 Sfax, Tunisia.
University of Sfax · TNHopital Universitaire Habib Bourguiba · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To further explore the epigenetic changes in nasopharyngeal carcinoma (NPC), methylation-sensitive arbitrarily primed PCR was performed on NPC biopsies and nontumor nasopharyngeal samples. We have shown mainly two DNA fragments that appeared to be differentially methylated in NPCs versus nontumors. The first, defined as hypermethylated, corresponds to a CpG island at the 5'-end of the tetratricopeptide repeat domain 40 (TTC40) gene, whereas the second, defined as hypo-methylated, is located on repetitive sequences at chromosomes 16p11.1 and 13.1. Thereafter, the epigenetic alteration on the 5'-TTC40 gene was confirmed by methylation-specific PCR, showing a significant aberrant methylation in NPCs, compared to nontumors. In addition, the bisulfite sequencing analysis has shown a very high density of methylated cytosines in C15, C17, and X666 NPC xenografts. To assess whether TTC40 gene is silenced by aberrant methylation, we examined the gene expression by reverse transcription-PCR. Our analysis showed that the mRNA expression was significantly lower in tumors than in nontumors, which is associated with 5'-TTC40 gene hypermethylation. In conclusion, we found that the 5'-TTC40 gene is frequently methylated and is associated with the loss of mRNA expression in NPCs. Hypermethylation of 5'-TTC40 gene might play a role in NPC development; nevertheless, other studies are needed.

Indexed as

Epigenesis, GeneticAnimalsAzacitidineCarcinomaCell Line, TumorCpG IslandsCytoskeletal ProteinsDNA MethylationGene Expression Regulation, NeoplasticHigh-Throughput Nucleotide SequencingHumansMiceNasopharyngeal CarcinomaNasopharyngeal NeoplasmsNeoplasm ProteinsPromoter Regions, GeneticAzacitidineCFAP46 protein, humanCytoskeletal ProteinsNeoplasm ProteinsProteins

Identifiers

PMID25101295
PMCPMC4101232
OpenAlexW2126715104

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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.