METTL14 Promotes Oral Squamous Cell Carcinoma Progression by Regulating the mRNA and m6A Levels of CALD1

被引:0
|
作者
Chen, Ruixue [1 ]
Zhang, Suxin [2 ,3 ]
Li, Hexiang [4 ]
Yang, Mengyuan [5 ]
Lu, Yiwen [5 ]
Zhang, Xudong [5 ]
机构
[1] Hebei Med Univ, Sch & Hosp Stomatol, Hebei Clin Res Ctr Oral Dis, Dept Endodont,Hebei Key Lab Stomatol, 383 Zhong Shan East Rd, Shijiazhuang, Hebei, Peoples R China
[2] Hebei Med Univ, Hosp 4, Dept Oral & Maxillofacial, 12 JianKang Rd, Shijiazhuang, Hebei, Peoples R China
[3] Hebei Med Univ, Hebei Tumor Hosp, 12 JianKang Rd, Shijiazhuang 50017, Hebei, Peoples R China
[4] Hebei Med Univ, Sch & Hosp Stomatol, Hebei Clin Res Ctr Oral Dis, Dept Pathol,Hebei Key Lab Stomatol, 383 Zhong Shan East Rd, Shijiazhuang, Hebei, Peoples R China
[5] Hebei Med Univ, Sch Hosp & Stomatol, Hebei Clin Res Ctr Oral Dis, Dept Oral & Maxillofacial,Hebei Key Lab Stomatol, 383 Zhong Shan East Rd, Shijiazhuang, Hebei, Peoples R China
关键词
METTL14; oral squamous cell carcinoma; CALD1; qRT-PCR; CALDESMON; DIFFERENTIATION; METHYLATION; METASTASIS;
D O I
暂无
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Oral squamous cell carcinoma (OSCC) still threatens people's daily life. METTL14 is a newly discovered methyltransferase that catalyzes m6A methylation. Hence, this research was carried out to investigate the action mechanism of METTL14 in OSCC. The SCC-4 and UM2 cells, and tumorigenicity assay were utilized to investigate METTL14 roles in vitro and in vivo. Bioinformatic analysis was carried out with the UCSC, TCGA database and The Human Protein Atlas. The gene expression at mRNA and protein levels were measured by qRT-PCR and Western blot. In addition, cell growth and metastasis was analyzed by colony formation and transwell assays. MeRIP assay was performed to test the m6A levels of CALD1. The METTL14 and CALD1 levels were prominently expressed in OSCC cells. METTL14 silencing depleted the cell growth and metastasis. Furthermore, METTL14 silencing depleted the tumor growth in vivo. Additionally, the mRNA and m6A levels of CALD1 were depleted after METTL14 silencing. Overexpressed CALD1 neutralized the si-METTL14 effects in OSCC cells. In conclusion, METTL14 participated in the OSCC progression through modulating the mRNA and m6A levels of CALD1.
引用
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页码:71 / 81
页数:11
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