LncRNA MIR503HG inhibits cell migration and invasion via miR‐103/OLFM4 axis in triple negative breast cancer

J Fu, G Dong, H Shi, J Zhang, Z Ning… - Journal of cellular …, 2019 - Wiley Online Library
J Fu, G Dong, H Shi, J Zhang, Z Ning, X Bao, C Liu, J Hu, M Liu, B Xiong
Journal of cellular and molecular medicine, 2019Wiley Online Library
Long non‐coding RNA MIR503 host gene (MIR503HG) is located on chromosome Xq26. 3,
and has been found to be deregulated in many types of human malignancy and function as
tumour suppressor or promoter based on cancer types. The role of MIR503HG in breast
cancer was still unknown. In our study, we found MIR503HG expression was significantly
decreased in triple‐negative breast cancer tissues and cell lines. Furthermore, we observed
low MIR503HG expression was correlated with late clinical stage, lymph node metastasis …
Abstract
Long non‐coding RNA MIR503 host gene (MIR503HG) is located on chromosome Xq26.3, and has been found to be deregulated in many types of human malignancy and function as tumour suppressor or promoter based on cancer types. The role of MIR503HG in breast cancer was still unknown. In our study, we found MIR503HG expression was significantly decreased in triple‐negative breast cancer tissues and cell lines. Furthermore, we observed low MIR503HG expression was correlated with late clinical stage, lymph node metastasis and distant metastasis. In the survival analysis, we observed that triple‐negative breast cancer patients with low MIR503HG expression had a statistically significant worse prognosis compared with those with high MIR503HG expression, and low MIR503HG expression was a poor independent prognostic factor for overall survival in triple‐negative breast cancer patients. The study in vitro suggested MIR503HG inhibits cell migration and invasion via miR‐103/OLFM4 axis in triple negative breast cancer. In conclusion, MIR503HG functions as a tumour suppressive long non‐coding RNA in triple negative breast cancer.
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