Evidence map›Paper›PMID 36946281›Full record

ArticleJournal of cellular and molecular medicine2023

Potential impact of ADAM-10 genetic variants with the clinical features of oral squamous cell carcinoma.

Yi-Tzu Chen, Chiao-Wen Lin, Ying-Erh Chou, Shih-Chi Su, Lun-Ching Chang, Chia-Yi Lee, Ming-Ju Hsieh, Shun-Fa Yang

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

15 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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  9. The impact of long non-coding RNAJournal of Cancer · 2025
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  14. The impact ofJournal of Cancer · 2023
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  15. The impacts ofJournal of Cancer · 2023
    Article
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 5 institutions in 2 countries.

Yi-Tzu ChenSchool of Dentistry, Chung Shan Medical University, Taichung, Taiwan.
Chiao-Wen LinDepartment of Dentistry, Chung Shan Medical University Hospital, Taichung, Taiwan.
Ying-Erh ChouSchool of Medicine, Chung Shan Medical University, Taichung, Taiwan.
Shih-Chi SuWhole-Genome Research Core Laboratory of Human Diseases, Chang Gung Memorial Hospital, Keelung, Taiwan.
Lun-Ching ChangDepartment of Mathematical Sciences, Florida Atlantic University, Boca Raton, Florida, USA.
Chia-Yi LeeInstitute of Medicine, Chung Shan Medical University, Taichung, Taiwan.
Ming-Ju HsiehOral Cancer Research Center, Changhua Christian Hospital, Changhua, Taiwan.ORCID 0000-0001-9726-3234
Shun-Fa YangDepartment of Medical Research, Chung Shan Medical University Hospital, Taichung, Taiwan.ORCID 0000-0002-0365-7927
Chung Shan Medical University Hospital · TWChang Gung Memorial Hospital · TWChung Shan Medical University · TWFlorida Atlantic University · USNational Chung Hsing University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A disintegrin and metalloproteinase domain-containing protein 10 (ADAM-10) involves in the tumour progression, but the impacts of single-nucleotide polymorphism (SNP) of ADAM-10 on oral squamous cell carcinoma (OSCC) remain unclear. The aim of this study was to investigate the influence of SNP of ADAM-10 on the clinical features of OSCC in male Taiwanese. Five loci of ADAM-10 SNPs including rs653765 (C/T), rs2305421 (A/G), rs514049 (A/C), rs383902 (T/C) and rs2054096 (A/T) were genotyped by TaqMan allelic discrimination in 1138 OSCC patients and 1199 non-OSCC individuals. The ADAM-10 SNP rs2305421 GG (AOR: 1.399, 95% CI: 1.045-1.874, p = 0.024) and G allele (AOR: 1.170, 95% CI: 1.012-1.351, p = 0.034) illustrated a significantly higher genotypic frequencies in the OSCC group compared to the distribution of the ADAM-10 SNP rs2305421 AA wild type. In the subgroup analysis, the ADAM-10 SNP rs383902 TC+CC was significantly correlated to tumour size larger than T2 in betel quid chewer (AOR: 1.375, 95% CI: 1.010-1.872, p = 0.043), while the ADAM-10 SNP rs653765 CT+TT was significantly associated with tumour size larger than T2 in cigarette smoker (AOR: 1.346, 95% CI: 1.023-1.772, p = 0.034). The results from The Cancer Genome Atlas revealed highest ADAM-10 mRNA level in T2 stage of current smokers with head and neck squamous cell carcinoma (HNSCC). In conclusions, the ADAM-10 SNP rs2305421 G allele is associated with the presence of OSCC, and the ADAM-10 SNP rs383902 TC+CC and ADAM-10 SNP rs653765 CT+TT correlates to large tumour size in specific conditions.

Indexed as

ADAM10 ProteinCarcinoma, Squamous CellMouth NeoplasmsCase-Control StudiesGenetic Predisposition to DiseaseHead and Neck NeoplasmsHumansMalePolymorphism, Single NucleotideRisk FactorsSquamous Cell Carcinoma of Head and NeckADAM10 ProteinADAM-10betel quidcigaretteoral squamous cell carcinomasingle-nucleotide polymorphisms

Identifiers

PMID36946281
PMCPMC10098292
OpenAlexW4353017169

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.