New insight into the radioresistance in breast cancer identify a dual function of miR-122 as tumor suppressor and oncomiR. New insight into the radioresistance in breast cancer identify a dual function of miR-122 as tumor suppressor and oncomiR

Through the use of antagomiR-122, the knockdown of miR-122 was achieved with an efficiency of 70% in the cell line MCF-7RR with phenotype of acquired resistance to ionizing radiation. To evaluate the transcriptomic landscape resulting from knockdown of miR-122 of radioresistant breast cancer cells MCF-7RR. These assays showed the modulation of genes enrichment in RAS-MAPK and TNFR signaling pathways, inflammatory response and regulation of transcription. Overall design: expression profile of genes from MCF-7RR cell line silenced by antagomir-122 (MCF7-122_1 and MCF7-122_2) versus MCF-7RR control without transfection (MCF-7RR_1 and MCF-7RR_2) using the Affymetrix Human Transcriptome Array 1.0 platform Array data was processed by Transcriptome Analysis Console (TAC).