| Literature DB >> 32729957 |
Yan Mao1, Meng Lv1, Weihong Cao1, Xiaoyi Liu1, Jian Cui1, Yongmei Wang1, Yuanyuan Wang1, Gang Nie1, Xiangping Liu2, Haibo Wang1.
Abstract
Increasing evidence indicates that circular RNAs (circRNAs) play a crucial role in regulating microRNAs (miRs) and mRNAs during breast cancer (BC) progression. Based on the in silico analysis of circRNA/miR/mRNA in BC, we aim to define an important role of circRNA_000554 in BC in relation to miR-182 and zinc finger protein 36 (ZFP36). Low expression of circRNA_000554 and ZFP36, and high miR-182 expression were determined in the clinical BC tissues. CircRNA_000554 acted as a sponge of miR-182, and miR-182 directly targeted ZFP36. After that, in order to evaluate the effects of circRNA_000554, miR-182, and ZFP36 on cellular process, we evaluated in vitro epithelial-mesenchymal transition (EMT) and in vivo tumor growth after delivering a series of overexpression plasmids, mimic, inhibitor, or shRNAs into BC cells. Increasing circRNA_000554 suppressed EMT, cell invasion and migration during BC by depleting miR-182 and increasing ZFP36. The inhibitory effect of circRNA_000554 on tumor growth was validated in vivo. Taken together, the present study confirms that circRNA_000554 functioned as an inhibitor of EMT in BC and suggests a molecular mechanism that circRNA_000554 bound to miR-182 to upregulate ZFP36 in this process.Entities:
Keywords: ZFP36; breast cancer; circular RNA 000554; epithelial-to-mesenchymal transition; microRNA-182
Year: 2020 PMID: 32729957 DOI: 10.1096/fj.201903047R
Source DB: PubMed Journal: FASEB J ISSN: 0892-6638 Impact factor: 5.191