Bioinformatics analysis of DNMT1 expression and its role in head and neck squamous cell carcinoma prognosis

被引:19
|
作者
Cui, Jili [1 ,2 ]
Zheng, Lian [2 ,3 ]
Zhang, Yuanyuan [1 ,2 ]
Xue, Miaomiao [1 ,2 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Dept Gen Dent, 1 Jianshe Rd, Zhengzhou 450052, Henan, Peoples R China
[2] Zhengzhou Univ, Affiliated Hosp 1, Key Lab Clin Med, Zhengzhou 450052, Henan, Peoples R China
[3] Zhengzhou Univ, Affiliated Hosp 1, Dept Oral & Maxillofacial Surg, Zhengzhou 450052, Henan, Peoples R China
关键词
MAMMALIAN DNA METHYLTRANSFERASES; GENE-EXPRESSION; METHYLATION; PROTEIN; TP53;
D O I
10.1038/s41598-021-81971-5
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Head and neck squamous cell carcinoma (HNSCC) is the sixth most common type of malignancy in the world. DNA cytosine-5-methyltransferase 1 (DNMT1) play key roles in carcinogenesis and regulation of the immune micro-environment, but the gene expression and the role of DNMT1 in HNSCC is unknown. In this study, we utilized online tools and databases for pan-cancer and HNSCC analysis of DNMT1 expression and its association with clinical cancer characteristics. We also identified genes that positively and negatively correlated with DNMT1 expression and identified eight hub genes based on protein-protein interaction (PPI) network analysis. Enrichment analyses were performed to explore the biological functions related with of DNMT1. The Tumor Immune Estimation Resource (TIMER) database was performed to explore the relationship between DNMT1 expression and immune-cell infiltration. We demonstrated that DNMT1 gene expression was upregulated in HNSCC and associated with poor prognosis. Based on analysis of the eight hub genes, we determined that DNMT1 may be involved in cell cycle, proliferation and metabolic related pathways. We also found that significant difference of B cells infiltration based on TP 53 mutation. These findings suggest that DNMT1 related epigenetic alterations have close relationship with HNSCC progression, and DNMT1 could be a novel diagnostic biomarker and a promising therapeutic target for HNSCC.
引用
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页数:11
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