A novel long non-coding RNA linc-ZNF469-3 promotes lung metastasis through miR-574-5p-ZEB1 axis in triple negative breast cancer.
Po-Shun WangCheng-Han ChouCheng-Han LinYun-Chin YaoHui-Chuan ChengHao-Yi LiYu-Chung ChuangChia-Ning YangLuo-Ping GerYu-Chia ChenForn-Chia LinTang-Long ShenMichael HsiaoPei-Jung Frank LuPublished in: Oncogene (2018)
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.
Keyphrases
- long non coding rna
- poor prognosis
- end stage renal disease
- newly diagnosed
- ejection fraction
- chronic kidney disease
- squamous cell carcinoma
- stem cells
- epithelial mesenchymal transition
- cell proliferation
- prognostic factors
- risk assessment
- blood brain barrier
- small molecule
- postmenopausal women
- oxidative stress
- cerebral ischemia
- functional connectivity
- pi k akt