Skip to main content
. 2020 Sep 14;11(11):3155–3167. doi: 10.1111/1759-7714.13634

Figure 4.

Figure 4

HAX1 promotes the survival of NSCLC cells via AKT/mTOR signaling pathway. (a) Phosphorylation of AKT, mTOR and 70S6K was inhibited in A549 and H1299 cells transfected with si‐HAX1. (b) Quantitative analysis of protein p‐AKT, p‐mTOR and p‐70S6K expression in A549 and H1299 cells. (Inline graphic) A549/si‐NC, (Inline graphic) H1299/si‐NC, (Inline graphic) A549/si‐HAX1 and (Inline graphic) H1299/si‐HAX1. (Inline graphic) A549/si‐NC, (Inline graphic) H1299/si‐NC, (Inline graphic) A549/si‐HAX1 and (Inline graphic) H1299/si‐HAX1. (Inline graphic) A549/si‐NC, (Inline graphic) H1299/si‐NC, (Inline graphic) A549/si‐HAX1 and (Inline graphic) H1299/si‐HAX1.(c) SC79 promoted the phosphorylation of AKT and mTOR in A549 and H1299 cells transfected with si‐HAX1. (d, e) Quantitative analysis of protein HAX1, p‐AKT, and p‐mTOR expression in A549 and H1299 cells. (f) TUNEL assays for apoptosis of A549 and H1299 cells transfected with si‐HAX1 after treatment of SC79. ***P < 0.001, **P < 0.01, *P < 0.05.