| Literature DB >> 32716347 |
Fengyun Hao1, Ya-Nan Bi2, Lei Wang3, Yubing Wang3, Jilei Ma3, Ping Cui3, Xuhua Li3, Shukai Sun4, Liang Ning5, Yichuan Huang1, Xuelong Jiao5, Dong Chen5.
Abstract
MicroRNAs (miRNAs) have been validated to play prominent roles in the occurrence and development of anaplastic thyroid carcinoma (ATC). miR-199a-5p was previously reported to act as a tumor suppressor or oncomiRNA in various types of cancer. However, its accurate expression, function, and mechanism in ATC remain unclear. Here, we find that miR-199a-5p is significantly downregulated in ATC tissues compared with adjacent non-cancerous tissues. Overexpression of miR-199a-5p significantly inhibits migration and invasion of ATC cells in vitro, and lung metastasis in vivo. Importantly, miR-199a-5p suppresses epithelial-mesenchymal transition (EMT) both in vitro and in vivo by targeting Snail. Taken together, this study reveals that miR-199a-5p is critical to the EMT progression in ATC cells. Targeting the pathway described here may be a novel approach for inhibiting metastasis of ATC.Entities:
Keywords: Anaplastic thyroid carcinoma; MicroRNAs; epithelial-mesenchymal transition; miR-199a-5p
Mesh:
Substances:
Year: 2020 PMID: 32716347 DOI: 10.3233/CBM-201518
Source DB: PubMed Journal: Cancer Biomark ISSN: 1574-0153 Impact factor: 3.828