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

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 sus...

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Published inScientific reports Vol. 15; no. 1; pp. 9956 - 9
Main Authors Lin, Chiao-Wen, Lu, Jeng-Wei, Chuang, Chun-Yi, Hsieh, Wang-Yu, Tsai, Yun-Jung, Yang, Shun-Fa, Lin, Shu-Hui
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Published London Nature Publishing Group UK 22.03.2025
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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.
AbstractList 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.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.
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.
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.
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.
ArticleNumber 9956
Author Lin, Chiao-Wen
Yang, Shun-Fa
Hsieh, Wang-Yu
Tsai, Yun-Jung
Lu, Jeng-Wei
Chuang, Chun-Yi
Lin, Shu-Hui
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  organization: Department of Bioscience and Biotechnology, National Taiwan Ocean University, Biotech Research and Innovation Centre, University of Copenhagen, The Finsen Laboratory, Faculty of Health and Medical Sciences, Rigshospitalet/National University Hospital, University of Copenhagen
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  givenname: Chun-Yi
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  fullname: Chuang, Chun-Yi
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  organization: Department of Pathology, Changhua Christian Hospital, Department of Post-Baccalaureate Medicine, College of Medicine, National Chung Hsing University, Department of Medical Laboratory Science and Biotechnology, Central Taiwan University of Science and Technology
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Issue 1
Keywords MIR155HG
Betel quid chewers
Single nucleotide polymorphism
Oral cancer
Language English
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Snippet 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...
Abstract Oral cancer is a malignant disease with a notably high incidence rate in Taiwan. Recent reports have revealed that MIR155HG polymorphisms play a...
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SubjectTerms 631/208
631/67
Adult
Aged
Alleles
Betel quid chewers
Cancer
Case-Control Studies
Cell differentiation
Clinical Relevance
Female
Gene polymorphism
Genetic diversity
Genetic Predisposition to Disease
Genetic variance
Genotype
Genotyping
Humanities and Social Sciences
Humans
Lymph nodes
Male
Metastases
Middle Aged
Minority & ethnic groups
MIR155HG
Mouth Neoplasms - genetics
Mouth Neoplasms - pathology
multidisciplinary
Oral cancer
Polymorphism
Polymorphism, Single Nucleotide
Population studies
RNA, Long Noncoding - genetics
Science
Science (multidisciplinary)
Single nucleotide polymorphism
Taiwan
Tumorigenesis
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Title Clinical significance of long non-coding RNA MIR155HG genetic variants and susceptibility to oral cancer
URI https://link.springer.com/article/10.1038/s41598-025-94661-3
https://www.ncbi.nlm.nih.gov/pubmed/40121375
https://www.proquest.com/docview/3180262921
https://www.proquest.com/docview/3180686988
https://pubmed.ncbi.nlm.nih.gov/PMC11929850
https://doaj.org/article/1ab28956ba1f4b049ec77226ca5977d5
Volume 15
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