| Literature DB >> 27904772 |
Huadong Zhao1, Haili Tang1, Qike Huang2, Bo Qiu1, Xiaomin Liu1, Dong Fan1, Li Gong3, Hang Guo4, Chong Chen5, Shixiong Lei1, Lu Yang6, Jianguo Lu1, Guoqiang Bao1.
Abstract
Increasing evidence suggests that microRNA-101 (miR-101) is involved in the progression of various human cancers, including papillary thyroid carcinoma (PTC). However, the biological functions of miR-101 and underlying molecular mechanisms in PTC remain largely unknown. In this study, we demonstrated that miR-101 underexpression in PTC tissue was associated with lymph node metastasis and poor prognosis of PTC patients. MiR-101 reduced PTC cell proliferation, apoptosis resistance, and invasion. Ubiquitin-specific protease 22 (USP22) was confirmed as a direct target of miR-101. USP22 restoration attenuated the inhibitory effects of miR-101 on PTC malignant traits in vitro. In vivo, miR-101 overexpression or USP22 depletion reduced the tumorigenesis of PTC. Overall, our findings provide new insight into the mechanism of PTC inhibition by miR-101, suggesting the potential of miR-101 as a therapeutic target in PTC patients.Entities:
Keywords: MicroRNA-101; papillary thyroid carcinoma; tumorigenesis; ubiquitin-specific protease 22
Year: 2016 PMID: 27904772 PMCID: PMC5126274
Source DB: PubMed Journal: Am J Cancer Res ISSN: 2156-6976 Impact factor: 6.166