Fig. 2
NEAT1 silencing repressed ATC cell migration, invasion and glycolysis under hypoxia. SW1736 and KAT-18 cells were exposed to 1% O2 or normoxia conditions for 48 h, or transfected with si-NEAT1 or si-NC before hypoxia exposure, followed by the determination of NEAT1 expression by qRT-PCR (a), cell migration (b) and invasion (c) by transwell assay, glucose consumption (d) and lactate production (e) using a corresponding assay kit, and HK2 expression by western blot (f). *P < 0.05