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. 2021 May 24;11:10765. doi: 10.1038/s41598-021-90143-4

Figure 5.

Figure 5

Abiraterone induces overexpression of lt-SLCO1B3 while suppressing hsa-miR-579-5p expression. Effects of abiraterone treatment on the expression of (a) lt-SLCO1B3 and (b) hsa-miR-579-3p in the samples processed for NanoString analysis were validated by qPCR analysis. As expected hsa-miR-579-3p expression was reduced and lt-SLCO1B3 expression was increased following abiraterone treatment, consistent with miRNA-transcript repression. (c) hsa-miR-579-3p directly binds to SLCO1B3 3′UTR. Co-transfection of 22Rv1 cells was performed with the 3′UTR reporter plasmid (or vector control plasmid) and hsa-miR-579-3p mimic (or negative control mimic) for 24 h followed by luciferase reporter assays. The assay revealed a significant decrease in SLCO1B3 reporter activity in the presence of the mimic. 22Rv1 cells were also transfected with the 3′UTR plasmid (or vector control plasmid) followed by treatment with 20 µM Abiraterone (or vehicle DMSO control) for 24 h. Abiraterone treatment resulted in an increase in SLCO1B3 luciferase reporter activity. No significant change was observed in the vector control plasmid lacking the 3′UTR (see Supplementary Fig. S4). These data are the results of three independent experiments performed in triplicates. ***P < 0.005, ****P < 0.0001.