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MicroRNA-182 targets FOXF2 to promote the development of triple-negative breast cancer

In: NEOPLASMA, vol. 64, no. 2
J. Yu - W. Shen - B. Gao - H. Zhao - J. Xu - B. Gong
Detaily:
Rok, strany: 2017, 209 - 215
O článku:
To explore the function of microRNA-182 (miR-182) on MCF7 and MDA-MB-231 cells behaviors, and possible mechanisms of triple-negative breast cancer (TNBC) development. Totally, 30 TNBC patients were enrolled to investigate the correlation between miR-182 expression and TNBC clinical indicators. miR-182 expression in TNBC tissues was measured by qRT-PCR, followed by bioinformatics methods and luciferase reporter assay to investigate whether FOXF2 was a direct target of miR-182. Besides, miR-182 mimics were transfected into MCF7 cells while miR-182 inhibitor into MDA-MB-231 cells, followed by cell proliferation and migration detection. miR-182 expression was significantly correlated with TNBC clinical indicators, such as lymph node metastasis TNM (stage III), intravascular cancer emboli and TNBC recurrence and metastasis. miR-182 expression was significantly higher in TNBC tissues than that in matched normal tissues, and was significantly higher in MDA-MB-231 cells than that in MCF7 cells. miR-182 knockdown inhibited the proliferation and migration of MDA-MB-231 cells while miR-182 overexpression markedly promoted the proliferation and migration of MCF7 cells. Besides, FOXF2 was identified as a direct target of miR-182. Our findings indicate that miR-182 may promote cell proliferation and migration in TNBC possible via down-regulation of FOXF2. miR-182 may serve as a potential target in TNBC treatment. Keywords: triple-negative breast cancer, microRNA-182, FOXF2, proliferation, migration
Ako citovať:
ISO 690:
Yu, J., Shen, W., Gao, B., Zhao, H., Xu, J., Gong, B. 2017. MicroRNA-182 targets FOXF2 to promote the development of triple-negative breast cancer. In NEOPLASMA, vol. 64, no.2, pp. 209-215. 0028-2685.

APA:
Yu, J., Shen, W., Gao, B., Zhao, H., Xu, J., Gong, B. (2017). MicroRNA-182 targets FOXF2 to promote the development of triple-negative breast cancer. NEOPLASMA, 64(2), 209-215. 0028-2685.