DNA甲基化
表观遗传学
生物
癌症研究
转移
甲状腺癌
甲基化
CpG站点
肿瘤科
癌
甲状腺癌
癌症
甲状腺
内科学
医学
遗传学
DNA
基因
基因表达
作者
Jin Peng,Qingfeng Zhang,Fei Lin,Chao Ke,Wuguo Deng,Ankui Yang,Xuan Su
出处
期刊:Epigenomics
[Future Medicine]
日期:2023-11-01
卷期号:15 (21): 1101-1119
标识
DOI:10.2217/epi-2023-0334
摘要
Aim: Conservative treatment approaches for thyroid carcinoma (TC) patients with wild-type B-type Raf kinase (BRAF) pose risks of long-term recurrence. The association of DNA methylation with TC metastasis is unclear. Patients & methods: Here we analyzed data from 179 BRAF wild-type TC patients in the The Cancer Genome Atlas database, identifying significant metastasis-associated CpGs. A logistic regression model was developed and validated for discriminating lymphatic metastasis in BRAF wild-type TC. Results: The model showed high accuracy (AUC: 0.924 training set; 0.812 and 0.773 external cohorts). TAGLN, MRPL4, CLDN10 and GRIK2 emerged as diagnostic markers. GRIK2, downregulated due to promoter hypermethylation, acted as a TC suppressor. Conclusion: Our 5-CpG epigenetic signature effectively discriminates lymphatic metastasis in BRAF wild-type TC, highlighting GRIK2's tumor-suppressive role influenced by promoter hypermethylation.
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