| Literature DB >> 31489990 |
Min Song1, Na Wang1, Zhen Li2, Yanfang Zhang1, Yingying Zheng1, Pengfei Yi1, Jing Chen1.
Abstract
The dysregulation of miR-125a-3p has been observed in multiple tumor types. Nevertheless, the function of miR-125a-3p in papillary thyroid carcinoma (PTC) is yet to be explored. Herein, we find that miR-125a-3p is markedly downregulated in PTC tissues, and its level is inversely related to the histological grade of PTC. Upregulation of miR-125a-3p suppresses the pulmonary metastatic ability as well as the tumor growth of PTC cell in vivo. Consistently, the colony formation ability and other metastasis-related traits of PTC cell are inhibited by miR-125a-3p transfection in vitro. In addition, we identify that matrix metalloprotease 11 (MMP11) is the direct target gene of miR-125a-3p, and that miR-125a-3p inhibits cell viability, migration, and invasiveness of PTC cell by reducing MMP11 expression in vitro. Together, these data testify that the miR-125a-3p/MMP11 axis plays vital roles in the growth and progression of human PTC cells.Entities:
Keywords: MMP11; PTC; metastasis; miR-125a-3p
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Year: 2019 PMID: 31489990 DOI: 10.1002/jcb.29333
Source DB: PubMed Journal: J Cell Biochem ISSN: 0730-2312 Impact factor: 4.429