Evidence map›Paper›PMID 26831400›Full record

ArticleScientific reports2016

Modulation of IL-1β reprogrammes the tumor microenvironment to interrupt oral carcinogenesis.

Tong Wu, Yun Hong, Lihua Jia, Jie Wu, Juan Xia, Juan Wang, Qinchao Hu, Bin Cheng

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% 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

52 citing papers in PubMed, 1 synthesis or guideline pooled it, 69 citations in OpenAlex.

  1. Pooled it
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  11. TheBiomolecules · 2025
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  17. The Role of IL-17 in the Pathogenesis of Oral Squamous Cell Carcinoma.International journal of molecular sciences · 2023
    Review
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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 2 institutions in 1 country.

Tong WuDepartment of Oral Medicine, Hospital of Stomatology, Sun Yat-sen University, Guangzhou, China.
Yun HongDepartment of Oral Medicine, Hospital of Stomatology, Sun Yat-sen University, Guangzhou, China.
Lihua JiaDepartment of Oral Medicine, Hospital of Stomatology, Sun Yat-sen University, Guangzhou, China.
Jie WuDepartment of Oral Medicine, Hospital of Stomatology, Sun Yat-sen University, Guangzhou, China.
Juan XiaDepartment of Oral Medicine, Hospital of Stomatology, Sun Yat-sen University, Guangzhou, China.
Juan WangDepartment of Oral Medicine, Hospital of Stomatology, Sun Yat-sen University, Guangzhou, China.
Qinchao HuDepartment of Oral Medicine, Hospital of Stomatology, Sun Yat-sen University, Guangzhou, China.
Bin ChengDepartment of Oral Medicine, Hospital of Stomatology, Sun Yat-sen University, Guangzhou, China.
Hospital of Stomatology, Sun Yat-sen UniversitySun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Head and neck squamous cell carcinoma (HNSCC) development is a multistage process includes the normal, dysplasia and squamous cell carcinoma (SCC) stages. Recently, increasing evidence has suggested that the tumor microenvironment (TME) is an integral part of malignant transformation. Exploring certain key node genes in TME for future intervention in dysplasia to interrupt oral carcinogenesis was the primary goal of this research. To achieve this goal, systems biology approaches were first applied to the epithelia and fibroblasts collected at sequential stages in a 4-nitroquinoline-1-oxide (4NQO) -induced rat oral carcinogenesis model. Through bioinformatics network construction, IL-1β was identified as one of the key node genes in TME during carcinogenesis. Immunohistochemical staining of human and rat samples demonstrated that IL-1β expression patterns were parallel to the stages of malignant transformation. Silencing IL-1β with lentivirus-delivered shRNA significantly inhibited oral squamous cell carcinoma cell growth both in vivo and in vitro. Based on these findings, we hypothesized that IL-1β may be a chemoprevention target in TME during oral carcinogenesis. Therefore, we targeted IL-1 in the TME by oral mucosal injection of an IL-1 receptor antagonist in 4NQO rats. The results demonstrated that targeting IL-1 could interrupt oral carcinogenesis by reprogramming the TME.

Indexed as

4-Nitroquinoline-1-oxideAdministration, OralAnimalsCarcinoma, Squamous CellCell Line, TumorCell Transformation, NeoplasticCluster AnalysisDisease Models, AnimalEpithelial-Mesenchymal TransitionFibroblastsGene Expression ProfilingGene SilencingHeterograftsInterleukin-1betaMaleModels, Biological4-Nitroquinoline-1-oxideInterleukin-1beta

Identifiers

PMID26831400
PMCPMC4735323
OpenAlexW2272547721

What OpenQuestion holds

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LicenceCC BY
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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.