| Literature DB >> 29755127 |
Po-Shun Wang1, Cheng-Han Chou1, Cheng-Han Lin1, Yun-Chin Yao1, Hui-Chuan Cheng1, Hao-Yi Li1, Yu-Chung Chuang2, Chia-Ning Yang2, Luo-Ping Ger3, Yu-Chia Chen4, Forn-Chia Lin5, Tang-Long Shen6, Michael Hsiao7,8, Pei-Jung Lu9,10.
Abstract
Triple-negative breast cancer (TNBC) patients usually lead to poor prognosis and survival because of metastasis. The major sites for TNBC metastasis include the lungs, brain, liver, and bone. Long non-coding RNAs (lncRNAs) are non-protein-coding transcripts longer than 200 nucleotides and have been reported as important regulators in BC metastasis. However, the underlying mechanisms for lncRNAs regulating TNBC metastasis are not fully understood. Here we found that linc-ZNF469-3 was highly expressed in lung-metastatic LM2-4175 TNBC cells and overexpression of linc-ZNF469-3 enhanced invasion ability and stemness properties in vitro and lung metastasis in vivo. Furthermore, we found linc-ZNF469-3 physically interacted with miR-574-5p and overexpression of miR-574-5p attenuated ZEB1 expression. Importantly, endogenous high expressions of linc-ZNF469-3 and ZEB1 were correlated with tumor recurrence in TNBC patients with lung metastasis. Taken together, our findings suggested that linc-ZNF469-3 promotes lung metastasis of TNBC through miR-574-5p-ZEB1 signaling axis and may be used as potential prognostic marker for TNBC patients.Entities:
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Year: 2018 PMID: 29755127 DOI: 10.1038/s41388-018-0293-1
Source DB: PubMed Journal: Oncogene ISSN: 0950-9232 Impact factor: 9.867