| Literature DB >> 31121562 |
Danrong Ye1, Yang Jiang1, Yihan Sun1, Yuefeng Li1, Yefeng Cai1, Qingxuan Wang1, Ouchen Wang1, Endong Chen1, Xiaohua Zhang1.
Abstract
Thyroid cancer is associated with one of the most malignant endocrine tumors. However, molecular mechanisms underlying thyroid tumorigenesis and progression remain unclear. In order to investigate these mechanisms, we performed whole-transcriptome sequencing, which indicated that a differentially expressed gene, METTL7B, was highly expressed in thyroid cancers. We analyzed METTL7B expression using TCGA and performed qRT-PCR on tissue samples. Moreover, an analysis of clinicopathological characteristics revealed a positive correlation between METTL7B and lymph node metastasis. A series of in vitro experiments indicated that METTL7B enhanced migration and invasion of thyroid carcinoma cells. Further studies revealed that METTL7B may enhance TGF-β1-induced epithelial-mesenchymal transition (EMT). Our results indicate that METTL7B may promote metastasis of thyroid cancer through EMT and may therefore be considered as a potential biomarker for the diagnosis and prognosis of thyroid carcinoma.Entities:
Keywords: METTL7B; epithelial-mesenchymal transition; metastasis; thyroid cancer
Year: 2019 PMID: 31121562 DOI: 10.1530/JME-18-0261
Source DB: PubMed Journal: J Mol Endocrinol ISSN: 0952-5041 Impact factor: 5.098