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

• Published in: Scientific 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
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 22.03.2025; Nature Publishing Group; Nature Portfolio
• Subjects: 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; Taiwan; MIR155HG; Betel quid chewers; Single nucleotide polymorphism; Oral cancer
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-025-94661-3

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.