Figure 1
Figure 1. MiR-29a is low expressed in ALK+ ALCL. (A) MiR-29a expression in ALK+ (SU-DHL-1, COST, PIO, Karpas-299) and ALK+ ALCL cells (FE-PD) was analyzed by RT-qPCR and Northern blotting. RNA from reactive lymph node (RLN) and peripheral blood mononuclear cells (PBMC) serve as normal controls. The histogram shows the relative expression (RQ) of miR-29a after normalization with RNU24. Bars represent standard deviations (SD). P for ALK+ vs controls and ALK+ vs ALK− (*P < .05). 5.8S RNA was used as the loading control in the Northern blotting. P for ALK+ vs controls (P < .001) and ALK+ vs ALK− (P < .05). (B) RT-qPCR of miR-29a in 20 ALK+ and 12 ALK− patient tumors. Three RLNs were used as normal controls. RQ was plotted on a logarithmic scale. P for ALK+ vs RLN and ALK+ vs ALK− (***P < .001).

MiR-29a is low expressed in ALK+ ALCL. (A) MiR-29a expression in ALK+ (SU-DHL-1, COST, PIO, Karpas-299) and ALK+ ALCL cells (FE-PD) was analyzed by RT-qPCR and Northern blotting. RNA from reactive lymph node (RLN) and peripheral blood mononuclear cells (PBMC) serve as normal controls. The histogram shows the relative expression (RQ) of miR-29a after normalization with RNU24. Bars represent standard deviations (SD). P for ALK+ vs controls and ALK+ vs ALK (*P < .05). 5.8S RNA was used as the loading control in the Northern blotting. P for ALK+ vs controls (P < .001) and ALK+ vs ALK (P < .05). (B) RT-qPCR of miR-29a in 20 ALK+ and 12 ALK patient tumors. Three RLNs were used as normal controls. RQ was plotted on a logarithmic scale. P for ALK+ vs RLN and ALK+ vs ALK (***P < .001).

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