| Literature DB >> 29563539 |
Jérôme Barbier1, Xin Chen1,2, Gabriel Sanchez1, Muyan Cai2, Marion Helsmoortel1, Takuma Higuchi3, Pierre Giraud1, Xavier Contreras1, Gangjun Yuan2, Zihao Feng4, Rima Nait-Saidi1, Olivier Deas5, Lisa Bluy1, Jean-Gabriel Judde5, Sylvie Rouquier1, William Ritchie6, Shuji Sakamoto3, Dan Xie7, Rosemary Kiernan8.
Abstract
Reduced expression of DICER, a key enzyme in the miRNA pathway, is frequently associated with aggressive, invasive disease, and poor survival in various malignancies. Regulation of DICER expression is, however, poorly understood. Here, we show that NF90/NF110 facilitates DICER expression by controlling the processing of a miRNA, miR-3173, which is embedded in DICER pre-mRNA. As miR-3173 in turn targets NF90, a feedback amplification loop controlling DICER expression is established. In a nude mouse model, NF90 overexpression reduced proliferation of ovarian cancer cells and significantly reduced tumor size and metastasis, whereas overexpression of miR-3173 dramatically increased metastasis in an NF90- and DICER-dependent manner. Clinically, low NF90 expression and high miR-3173-3p expression were found to be independent prognostic markers of poor survival in a cohort of ovarian carcinoma patients. These findings suggest that, by facilitating DICER expression, NF90 can act as a suppressor of ovarian carcinoma.Entities:
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Year: 2018 PMID: 29563539 PMCID: PMC5951825 DOI: 10.1038/s41422-018-0016-8
Source DB: PubMed Journal: Cell Res ISSN: 1001-0602 Impact factor: 25.617