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. Author manuscript; available in PMC: 2020 Nov 1.

Published in final edited form as: Cytokine. 2019 Jul 25;123:154789. doi: 10.1016/j.cyto.2019.154789

Figure 5. — A) miR-590–5 expression levels were measured in activated (gray bar) LX-2 cells and cells grown on Matrigel (black bar). B) LX-2 cells were treated with 250 ng/mL CCL20 (CCL20: gray bar) or untreated (NTC: black bar) for six hours. Data were normalized using RNU48 and RNU6B. The −ΔΔCt method was used to determine fold-change of miR-590-5p expression. All experiments were performed in triplicate. *P<0.05.

Figure 5. — A) miR-590–5 expression levels were measured in activated (gray bar) LX-2 cells and cells grown on Matrigel (black bar). B) LX-2 cells were treated with 250 ng/mL CCL20 (CCL20: gray bar) or untreated (NTC: black bar) for six hours. Data were normalized using RNU48 and RNU6B. The −ΔΔCt method was used to determine fold-change of miR-590-5p expression. All experiments were performed in triplicate. *P<0.05.