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. 2021 Oct 9;21:525. doi: 10.1186/s12935-021-02232-z

Fig. 3.

Fig. 3

AL355338 facilitated aggressive phenotypes and glycolytic metabolism of NSCLC cells. AC The migratory and invasive activities of AL355338 was detected by transwell assays in A549 and PC9 cells transfected with AL355338 siRNAs or si-NC. Representative images and quantitative analysis were shown. Scale bar, 50 μm. DF Representative images and quantitative analysis of wound healing assays for the indicated cells. Scale bar, 100 μm. G Western blot analysis was performed to detect EMT markers (E-cadherin, N-cadherin, Vimentin) in indicated cells. H HK2, PKM2 and LDHA protein expressions were examined under AL355338 knockdown conditions by western blotting. I 18F-FDG uptake level was detected in A549 and PC9 cells transfected with AL355338 siRNAs or si-NC. J Lactate release level was measured for the indicated cells. K ATP production level was determined for the indicated cells. Data shown are mean ± SD (n = 3) (*P < 0.05, **P < 0.01, ***P < 0.001)