Evidence map›Paper›PMID 40121375›Full record

ArticleScientific reports2025

Clinical significance of long non-coding RNA MIR155HG genetic variants and susceptibility to oral cancer.

Chiao-Wen Lin, Jeng-Wei Lu, Chun-Yi Chuang, Wang-Yu Hsieh, Yun-Jung Tsai, Shun-Fa Yang, Shu-Hui Lin

Abstract read
In one paragraph

Article in Scientific reports, 2025. 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
–field-weighted citation impact
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.

  1. Review
  2. Clinical Relevance ofInternational journal of molecular sciences · 2025
    Article
  3. International journal of medical sciences · 2025
    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

7 authors.

Chiao-Wen Lin *Institute of Oral Sciences, Chung Shan Medical University, Taichung, Taiwan.
Jeng-Wei Lu *Department of Bioscience and Biotechnology, National Taiwan Ocean University, Keelung, Taiwan.
Chun-Yi ChuangDepartment of Otolaryngology, Chung Shan Medical University Hospital, Taichung, Taiwan.
Wang-Yu HsiehMing Dao Senior High School, Taichung, Taiwan.
Yun-Jung TsaiTranslational pathology core laboratory, Changhua Christian Hospital, Changhua, Taiwan.
Shun-Fa YangInstitute of Medicine, Chung Shan Medical University, Taichung, Taiwan.
Shu-Hui LinDepartment of Pathology, Changhua Christian Hospital, Changhua, Taiwan. 74630@cch.org.tw.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oral cancer is a malignant disease with a notably high incidence rate in Taiwan. Recent reports have revealed that MIR155HG polymorphisms play a crucial role in the development of tumorigenesis in human cancers. The objective of this study was to investigate the role of MIR155HG polymorphisms in susceptibility to oral cancer among individuals in the Taiwanese Han population. In this study, we recruited 1316 oral cancer patients and controls to investigate the allelic discrimination of MIR155HG polymorphisms. Genotyping was performed using a TaqMan allelic discrimination test. The association of MIR155HG polymorphism rs1893650 with oral cancer susceptibility was found to be significant, unlike rs928883, rs767649, rs72014506, and rs4143370. Moreover, when compared to the homozygous TT genotype, the C alleles of rs1893650 polymorphism showed a significant correlation with cell differentiation grade in oral cancer patients (p = 0.019). Additionally, in oral cancer patients who chew betel quid, the C alleles of the rs1893650 polymorphism was significantly associated with lymph node metastasis and cell differentiation grade compared to those with the homozygous TT genotype. It was concluded that the rs1893650 polymorphism significantly increased the likelihood of developing oral cancer. Further large-scale studies involving diverse ethnic populations and clinicopathological characteristics are required to confirm these results. This research paves the way for new approaches in the detection and diagnosis of oral cancer, enabling early prevention of this disease.

Indexed as

Genetic Predisposition to DiseaseMouth NeoplasmsPolymorphism, Single NucleotideRNA, Long NoncodingAdultAgedAllelesCase-Control StudiesClinical RelevanceFemaleGenotypeHumansMaleMiddle AgedTaiwanRNA, Long NoncodingBetel quid chewersMIR155HGOral cancerSingle nucleotide polymorphism

Identifiers

PMID40121375
PMCPMC11929850

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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 Socratic graph.