Evidence map›Paper›PMID 31530984›Full record

ArticleCentral-European journal of immunology2019

Increased risks between TLR2 (-196 to -174 ins/del) and TLR3 1377C>T variants and head and neck cancers in Tunisia.

Lamia Makni, Sabrina Zidi, Mouadh Barbiroud, Amira Ben Ahmed, Ezzedine Gazouani, Amel Mezlini, Mouna Stayoussef, Besma Yacoubi-Loueslati

Open access · goldAbstract read
In one paragraph

Article in Central-European journal of immunology, 2019. 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
0.5field-weighted citation impact, top 33% 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, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Characterization and strong risk association ofWorld journal of gastrointestinal oncology · 2020
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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 4 institutions in 1 country.

Lamia MakniLaboratory of Mycology, Pathologies, and Biomarkers: LR16ES05, Department of Biology, Faculty of Sciences, El Manar University, Tunis, Tunisia.
Sabrina ZidiLaboratory of Mycology, Pathologies, and Biomarkers: LR16ES05, Department of Biology, Faculty of Sciences, El Manar University, Tunis, Tunisia.
Mouadh BarbiroudLaboratory of Venoms and Therapeutic Molecules, Pasteur Institute of Tunisia, El Manar University, Tunis, Tunisia.
Amira Ben AhmedLaboratory of Mycology, Pathologies, and Biomarkers: LR16ES05, Department of Biology, Faculty of Sciences, El Manar University, Tunis, Tunisia.
Ezzedine GazouaniLaboratory of Immunology, Military Hospital of Tunis, Tunis, Tunisia.
Amel MezliniSalah Azeiz Oncology Institute, Tunis, Tunisia.
Mouna StayoussefLaboratory of Mycology, Pathologies, and Biomarkers: LR16ES05, Department of Biology, Faculty of Sciences, El Manar University, Tunis, Tunisia.
Besma Yacoubi-LoueslatiLaboratory of Mycology, Pathologies, and Biomarkers: LR16ES05, Department of Biology, Faculty of Sciences, El Manar University, Tunis, Tunisia.
Tunis El Manar University · TNInstitut Pasteur de Tunis · TNInstitut Salah-Azaïz · TNMilitary Hospital of Tunis · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPrevious studies have highlighted the importance of polymorphisms of toll-like receptors (TLRs) in the pathogenesis of certain cancers, including head and neck cancers (HNC). AIM OF THE STUDY: The aim of this study was to evaluate the association of TLR2 (-196 to -174 ins/del) and TLR3 (1377 C>T) as potential risk factors for HNC in Tunisians. MATERIAL AND

methodsA case-control study including 246 HNC patients (174 nasopharyngeal carcinoma - NPC and 72 laryngeal cancer - LC) and 250 healthy controls. Genotyping was done by using PCR and PCR-RFLP methods.

resultsHigher minor allele frequencies of TLR2 (-196 to -174 ins/del) and TLR3 1377 C>T polymorphisms were seen in HNC, NPC, and LC compared to controls. In addition, higher increased HNC, NPC, and LC risk was associated with TLR2 ins/del and TLR2 del/del genotypes (p < 0.0001). Positive association with HNC, NPC, and LC risk was seen with TLR2 del-containing genotypes (ins/del + del/del) (p < 0.0001). The T/T genotype of TLR3 is associated with HNC, NPC, and LC susceptibility (p < 0.0001). Positive association with HNC and NPC risk was seen with TLR3 T allele carriers (C/T + T/T) (p < 0.0001). Increased frequency of T-ins, C-del, and T-del haplotypes was revealed in HNC and NPC cases than healthy controls; however, T-del was significantly higher in LC cases.

conclusionsOur results demonstrate an increased risk of HNC, NPC, and LC with TLR2 ins/del, TLR2 del/del, and TLR3 T/T genotypes. And positive association with T-ins, C-del, and T-del haplotypes with HNC and NPC and T-del haplotype with LC.

Indexed as

head and neck cancerlaryngeal cancernasopharyngeal cancerpolymorphismstoll-like receptorsTunisia

Identifiers

PMID31530984
PMCPMC6745549
OpenAlexW2969084046

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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.