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. Author manuscript; available in PMC: 2015 May 1.
Published in final edited form as: Cancer Lett. 2014 Jan 14;346(2):257–263. doi: 10.1016/j.canlet.2014.01.002

Fig. 4.

Fig. 4

Silencing STAT3 and JNK repressed mdig expression. A. BEAS-2B cells were transfected with 50 nM control siRNA (siCtrl), or STAT3 specific siRNA (siSTAT3) and cultured for 24 h. Cells were cultured in the presence of 20 μM As3+ for an additional 2 h. The levels of STAT3 activation, mdig protein, JNK and Akt activation were determined by Westernblotting. B. Silencing JNK2, but not JNK1, reduced the levels of basal and As3+-induced mdig. Cell transfection with siRNA and treatment are the same as in A.