Academy of Basic Medicine, Jining Medical University, Jining, China.
Clinical Medical School, Jining Medical University, Jining, China.
J Cell Mol Med. 2019 Jul;23(7):4738-4745. doi: 10.1111/jcmm.14344. Epub 2019 May 6.
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.
长非编码 RNA MIR503 宿主基因(MIR503HG)位于染色体 Xq26.3,已在多种人类恶性肿瘤中发现失调,并根据癌症类型发挥肿瘤抑制或促进作用。MIR503HG 在乳腺癌中的作用尚不清楚。在我们的研究中,我们发现 MIR503HG 在三阴性乳腺癌组织和细胞系中的表达显著降低。此外,我们观察到低 MIR503HG 表达与晚期临床分期、淋巴结转移和远处转移相关。在生存分析中,我们观察到低 MIR503HG 表达的三阴性乳腺癌患者与高 MIR503HG 表达的患者相比,预后有统计学意义上的显著恶化,低 MIR503HG 表达是三阴性乳腺癌患者总生存的不良独立预后因素。体外研究表明,MIR503HG 通过 miR-103/OLFM4 轴抑制三阴性乳腺癌细胞的迁移和侵袭。总之,MIR503HG 在三阴性乳腺癌中作为一种肿瘤抑制性长非编码 RNA 发挥作用。