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rs13181449变异体降低口腔癌发生风险。

rs13181449 variant decreases the risk of oral cancer development.

作者信息

Hung Li-Chung, Huang Cheng-Chen, Lu Yen-Ting, Su Chun-Wen, Lin Chiao-Wen, Chu Hsiao-Ju, Yang Shun-Fa, Lu Hsueh-Ju

机构信息

Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan.

Department of Radiation Oncology, Changhua Christian Hospital, Changhua, Taiwan.

出版信息

Int J Med Sci. 2025 Jun 20;22(12):3022-3031. doi: 10.7150/ijms.113676. eCollection 2025.


DOI:10.7150/ijms.113676
PMID:40657390
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12243962/
Abstract

NOP2/Sun RNA methyltransferase 2 (NSUN2), encoded by the gene, is a nuclear RNA methyltransferase that catalyzes the methylation of cytosine to 5-methylcytosine (m5C). Although RNA modification has been widely discussed in cancer development and prognosis, the role of the gene in oral cavity squamous cell carcinoma (OCSCC) is unclear. This was a retrospective, case-control study. A total of 2514 participants were enrolled, including 52.4% (1318/2514) diagnosed with OCSCC and others as health control. The impact of rs4702373, rs166049, rs13181449, and rs8192120 on cancer development and prognosis were analyzed. Our results revealed that rs13181449 allele TT was significantly associated with lower OCSCC risk, with an adjusted odd ratio (AOR) [95% confidence index (CI)] of 0.757[0.575-0.997]. For cigarette smokers, the impact of rs13181449 was more obvious that AOR [95% CI] of allele CT, TT, and CT+TT were 0.760 [0.583-0.991], 0.699 [0.493-0.990], 0.746 [0.580-0.960], respectively. For OCSCC patients, rs4702373 allele CT was independently associated with advanced histological grade. Expression levels between different allele mutations were various in the GTE database. Mutant rs4702373 and rs166049 were associated with higher expression than the wild type, conversely mutant rs13181449 had lower expression. In the TCGA database, the trend that patients with higher expression had worse survival than those with lower expression was shown. In conclusion, rs13181449 was associated with lower cancer risk, especially for cigarette smokers. Unlikely other allele mutations, rs13181449 was correlated to lower expression. Patients with higher expression had worsened clinical outcomes.

摘要

由该基因编码的NOP2/Sun RNA甲基转移酶2(NSUN2)是一种核RNA甲基转移酶,可催化胞嘧啶甲基化为5-甲基胞嘧啶(m5C)。尽管RNA修饰在癌症发展和预后方面已被广泛讨论,但该基因在口腔鳞状细胞癌(OCSCC)中的作用尚不清楚。这是一项回顾性病例对照研究。共纳入2514名参与者,其中52.4%(1318/2514)被诊断为OCSCC,其他为健康对照。分析了rs4702373、rs166049、rs13181449和rs8192120对癌症发展和预后的影响。我们的结果显示,rs13181449等位基因TT与较低的OCSCC风险显著相关,调整后的优势比(AOR)[95%置信区间(CI)]为0.757[0.575-0.997]。对于吸烟者,rs13181449的影响更为明显,等位基因CT、TT和CT+TT的AOR[95%CI]分别为0.760[0.583-0.991]、0.699[0.493-0.990]、0.746[0.580-0.960]。对于OCSCC患者,rs4702373等位基因CT与高级别组织学分级独立相关。在GTE数据库中,不同等位基因突变之间的表达水平各不相同。突变型rs4702373和rs166049的表达高于野生型,相反,突变型rs13181449的表达较低。在TCGA数据库中,显示出表达较高的患者生存率低于表达较低的患者的趋势。总之,rs13181449与较低的癌症风险相关,尤其是对于吸烟者。与其他等位基因突变不同,rs13181449与较低的表达相关。表达较高的患者临床结局较差。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f6d/12243962/a3bc5692c3e8/ijmsv22p3022g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f6d/12243962/51d5f91aed96/ijmsv22p3022g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f6d/12243962/a3bc5692c3e8/ijmsv22p3022g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f6d/12243962/51d5f91aed96/ijmsv22p3022g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f6d/12243962/a3bc5692c3e8/ijmsv22p3022g002.jpg

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本文引用的文献

[1]
Clinical significance of long non-coding RNA MIR155HG genetic variants and susceptibility to oral cancer.

Sci Rep. 2025-3-22

[2]
The Impact of Variants in Oral Cancer Progression and Clinicopathological Characteristics.

J Cancer. 2025-2-11

[3]
Associations of the Expression Levels and Risk Variants of CDKN2B-AS1 Long Noncoding RNA With the Susceptibility and Progression of Prostate Cancer.

J Cell Mol Med. 2024-12

[4]
Prognostic impact of caspase-8 mutation in oral cavity squamous cell carcinoma.

Oral Dis. 2025-3

[5]
NSUN2/YBX1 promotes the progression of breast cancer by enhancing HGH1 mRNA stability through mC methylation.

Breast Cancer Res. 2024-6-6

[6]
NSUN2 promotes lung adenocarcinoma progression through stabilizing PIK3R2 mRNA in an mC-dependent manner.

Mol Carcinog. 2024-5

[7]
Emerging role of RNA modification and long noncoding RNA interaction in cancer.

Cancer Gene Ther. 2024-6

[8]
Genetic and environmental contributions for the relationship between tooth loss and oral potentially malignant disorders and oral squamous cell carcinoma.

Head Neck. 2024-6

[9]
IGF2BP2 promotes cell invasion and epithelial-mesenchymal transition through Src-mediated upregulation of EREG in oral cancer.

Int J Biol Sci. 2024

[10]
Polymorphisms associated with oral clefts as potential markers for oral pre and malignant disorders.

Oral Dis. 2024-7

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