Evidence map›Paper›PMID 30127645›Full record

ReviewCancer management and research2018

Association of IL-8 gene promoter -251 A/T and IL-18 gene promoter -137 G/C polymorphisms with head and neck cancer risk: a comprehensive meta-analysis.

Zheng Wang, Zi-Ming Gao, Hai-Bo Huang, Li-Sha Sun, An-Qi Sun, Kai Li

Open access · goldAbstract readReview
In one paragraph

Review in Cancer management and research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Interleukin-18 in Health and Disease.International journal of molecular sciences · 2019
    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 2 institutions in 1 country.

Zheng WangDepartment of Otorhinolaryngology, the First Affiliated Hospital of China Medical University, Shenyang 110001, China.
Zi-Ming GaoDepartment of Surgical Oncology, the First Affiliated Hospital of China Medical University, Shenyang 110001, China, cmu_likai@hotmail.com.
Hai-Bo HuangDepartment of Surgical Oncology, the First Affiliated Hospital of China Medical University, Shenyang 110001, China, cmu_likai@hotmail.com.
Li-Sha SunDepartment of Surgical Oncology, the First Affiliated Hospital of China Medical University, Shenyang 110001, China, cmu_likai@hotmail.com.
An-Qi SunDepartment of Surgical Oncology, the First Affiliated Hospital of China Medical University, Shenyang 110001, China, cmu_likai@hotmail.com.
Kai LiDepartment of Surgical Oncology, the First Affiliated Hospital of China Medical University, Shenyang 110001, China, cmu_likai@hotmail.com.
China Medical University · CNFirst Hospital of China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeNo consensus exists on the impact of polymorphisms in cytokines (such as interleukin IL-8 and IL-18) on cancer risk; moreover, there is very little evidence regarding head and neck cancer (HNC).

methodsThus, a meta-analysis including 22 studies with 4731 cases and 8736 controls was conducted to evaluate this association. The summary odds ratio (OR) and corresponding 95% confidence intervals (CIs) for C-X-C motif chemokine ligand 8 (CXCL8, which encodes IL-8) and IL-18 polymorphisms and HNC risk were estimated.

resultsThe results showed a significantly increased risk of HNC susceptibility for IL18 -137 G/C in five genetic models, but, interestingly, no significant association was found for the CXCL8 -251 A/T polymorphism. When stratified by cancer type, an increased risk of nasopharyngeal cancer was found for both -137 G/C and -251A/T. When the studies were stratified by ethnicity and genotyping method, there were significant associations between Asian populations and polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) studies for -137 G/C, and African populations for -251 A/T in some genetic models. A positive association was also found between the population-based groups in some models for -137 G/C; conversely, significantly decreased risk was found among the -251 A/T hospital-based group. Meta-regression was also conducted. The publication year, control source, and cancer type contributed to CXCL8 -251 A/T heterogeneity; however, no factors were found that contributed to IL-18 -137 G/C heterogeneity. Marginal significance was found in the recessive model for IL-18 -137 G/C by Egger's test, whereas no publication bias was detected for CXCL8 -251 A/T.

conclusionsThe results indicate that the IL-18 -137 G/C polymorphism is associated with HNC risk, especially nasopharyngeal cancer, in Asian populations and, when using PCR-RFLP, CXCL8 -251 A/T polymorphisms play a complex role in HNC development.

Indexed as

head and neck cancerinterleukin-18interleukin-8meta-analysispolymorphism

Identifiers

PMID30127645
PMCPMC6089118
OpenAlexW2887633239

What OpenQuestion holds

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LicenceCC BY-NC
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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.