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. 2017 Jun 18;11(9):1189–1207. doi: 10.1002/1878-0261.12088

Figure 6.

Figure 6

Specific blockade of TrkA by siRNA decreases cell viability and proliferation and downregulates the phosphorylation of survival‐promoting proteins in NPM‐ALK + T‐cell lymphoma cells. Transfection of TrkA siRNA decreased the (A) viability and (B) proliferation of SR‐786 cells. Data represent means ± SE of three independent experiments (*< 0.001 vs. scrambled siRNA‐transfected cells). (C) The decrease in TrkA was associated with decreased phosphorylation of NPM‐ALK, IGF‐IR, AKT, and STAT3. β‐Actin was used as the loading control. MW: TrkA and pTrkA, 140 kDa; NPM‐ALK and pNPM‐ALK, 80 kDa; IGF‐IR and pIGF‐IR, 95 kDa; AKT and pAKT, 60 kDa; STAT3 and pSTAT3, 86 kDa.