Abstract
Accumulating data have shown the involvement of microRNAs in cancerous processes as either oncogenes or tumor suppressor genes. Here, we established miR-30a as a tumor suppressor gene in breast cancer development and metastasis. Ectopic expression of miR-30a in breast cancer cell lines resulted in the suppression of cell growth and metastasis in vitro. Consistently, the xenograft mouse model also unveiled the suppressive effects of miR-30a on tumor growth and distal pulmonary metastasis. With dual luciferase reporter assay, we revealed that miR-30a could bind to the 3′-untranslated region of metadherin (MTDH) gene, thus exerting inhibitory effect on MTDH. Furthermore, we demonstrated that silence of MTDH could recapitulate the effects of miR-30a overexpression, while overexpression of MTDH could partially abrogate miR-30a-mediated suppression. Of significance, expression level of miR-30a was found to be significantly lower in primary breast cancer tissues than in the paired normal tissues. Further evaluation verified that miR-30a was negatively correlated with the extent of lymph node and lung metastasis in patients with breast cancer. Taken together, our findings indicated miR-30a inhibits breast cancer proliferation and metastasis by directly targeting MTDH, and miR-30a can serve as a prognostic marker for breast cancer. Manipulation of miR-30a may provide a promising therapeutic strategy for breast cancer treatment.
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Acknowledgements
We thank Shi Yan, Cunzhong Yuan and Ning Yang for collecting the clinical samples. This work was supported by National Natural Science Foundation of China (no. 30772133; no. 81072150; no. 81172529; no. 81272903) and Shandong Science and Technology Development Plan (no. 2012GZC22115).
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Zhang, N., Wang, X., Huo, Q. et al. MicroRNA-30a suppresses breast tumor growth and metastasis by targeting metadherin. Oncogene 33, 3119–3128 (2014). https://doi.org/10.1038/onc.2013.286
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DOI: https://doi.org/10.1038/onc.2013.286
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