| Literature DB >> 31213131 |
Liang Xia1, Linlin Wu2, Hailong Xia1, Jing Bao1, Qingsheng Li1, Xiaowen Chen1, Ruixiang Xia1.
Abstract
Cutaneous T-cell lymphoma (CTCL) is associated with the downregulation of miR-337 expression, although the exact underlying mechanism is unknown. In the present work, we investigated the molecular mechanism and function of miR-337 in regulating CTCL cell viability and invasion. We observed that miR-337 expression was downregulated in both CTCL tumors and cell lines. Furthermore, CCK assay, BrdU incorporation assay, and flow cytometry revealed that transfection with the miR-337 mimic resulted in decreased proliferation and increased apoptotic levels in CTCL cells. Results of the Transwell migration assay indicated that the miR-337 mimic decreased CTCL cell invasion in vitro. Both bioinformatics prediction and the dual-luciferase reporter assay revealed that miR-337 targets the 3'-UTR of STAT3 for silencing. Overexpression of STAT3 counteracted the pro-apoptotic influence of miR-337 in CTCL cell lines and restored their invasion properties. The results thus indicate that the miR-337-STAT3 axis inhibits the proliferation of malignant T cells and that miR-337 may serve as a promising therapeutic target for CTCL.Entities:
Keywords: Cutaneous T-cell lymphoma; metastasis; miR-337
Year: 2019 PMID: 31213131 PMCID: PMC6619951 DOI: 10.1080/15384101.2019.1629789
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534