Evidence map›Paper›PMID 30160047›Full record

ArticleMolecular genetics & genomic medicine2018

Joint effect of smoking and NQO1 C609T polymorphism on undifferentiated nasopharyngeal carcinoma risk in a North African population.

Khalid Moumad, Wafa Khaali, Abdellatif Benider, Wided Ben Ayoub, Mokhtar Hamdi-Cherif, Kada Boualga, Elham Hassen, El Khalil Ben Driss, Marilys Corbex, Meriem Khyatti

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In one paragraph

Article in Molecular genetics & genomic medicine, 2018. 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
0.6field-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

3 citing papers in PubMed, 8 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 8 institutions in 5 countries.

Khalid MoumadOncovirology Laboratory, Institut Pasteur du Maroc, Casablanca, Morocco.
Wafa KhaaliOncovirology Laboratory, Institut Pasteur du Maroc, Casablanca, Morocco.
Abdellatif BeniderService de Radiothérapie, Centre d'oncologie Ibn Rochd, Casablanca, Morocco.
Wided Ben AyoubAssociation Tunisienne de Lutte Contre le Cancer, Tunis, Tunisia.
Mokhtar Hamdi-CherifService d'épidémiologie, CHU de Sétif, Sétif, Algeria.
Kada BoualgaService de Radiothérapie Oncologique, Centre Antic-Cancer de Blida, Blida, Algeria.
Elham HassenMolecular Immuno-Oncology Laboratory, Faculty of Medicine, Monastir University, Monastir, Tunisia.
El Khalil Ben DrissDepartement of Biology, Faculty of Sciences, Abdelmalek Essaadi University, Tetouan, Morocco.
Marilys CorbexWho Regional Office for Europe, Copenhagen, Denmark.
Meriem KhyattiOncovirology Laboratory, Institut Pasteur du Maroc, Casablanca, Morocco.ORCID 0000-0001-9376-4322
Institut Pasteur · FRAbdelmalek Essaâdi University · MAAssociation Tunisienne Contre le Cancer · TNCentre Hospitalier Universitaire Ibn Rochd · MACentre Hospito Universitaire de Sétif · DZUniversity of Blida · DZUniversity of Monastir · TNWorld Health Organization Regional Office for Europe · DK

Funding

World Health Organization 001
6 · The paper itself

Abstract

backgroundNasopharyngeal carcinoma (NPC) has a higher incidence in North Africa than in most parts of the world. In addition to environmental factors such as Epstein-Barr virus infection and chemical carcinogen exposure, genetic susceptibility has been reported to play a key role in the development of NPC. NAD(P)H: quinone oxidoreductase 1 is a cytosolic enzyme that protects cells from oxidative damage. A C to T transition at position 609 in the NQO1 gene (OMIM: 125860) has been shown to alter the enzymatic activity of the enzyme and has been associated with increased risk to several cancers. This study investigates for the first time the effect of this polymorphism on NPC susceptibility in a North African population.

methodsThe NQO1 C609T polymorphism was genotyped using PCR-RFLP in 392 NPC cases and 365 controls from Morocco, Algeria, and Tunisia.

resultsThe allele frequencies and distributions of genotypes did not differ between cases and controls (p > 0.05). When stratifying according to smoking status, we observed two-fold higher NPC risk in ever-smokers carrying the CT or TT genotype. Multiple logistic regression analysis revealed that there was a significant interaction between T allele and smoking status (OR = 1.95, 95% CI = 1.20-3.19; interaction p = 0.007).

conclusionIn this North African population, the functional NQO1 polymorphism was associated with a significantly higher risk of NPC among smokers and did not affect the risk among nonsmokers.

Indexed as

Polymorphism, Single NucleotideAdultAfrica, NorthernFemaleHumansMaleMiddle AgedNAD(P)H Dehydrogenase (Quinone)Nasopharyngeal CarcinomaNasopharyngeal NeoplasmsSmokingNAD(P)H Dehydrogenase (Quinone)NQO1 protein, humannasopharyngeal carcinomaNorth AfricaNQO1 polymorphismsmoking

Identifiers

PMID30160047
PMCPMC6305636
OpenAlexW2889406105

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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.