Fig. 2.

Silencing of SNHG5 repressed BC cell proliferation and glycolysis. A QRT-PCR detected the knockdown efficiency of sh-SNHG5. Sh-SNHG5, sh-NC or control were transfected into BC cells. B Cell proliferation was analyzed by colony formation assay. C Cell cycle was examined by flow cytometry. D Glucose consumption and E lactate production were analyzed by the corresponding kit. F HK2, PFK1 and GAPDH protein expression were determined by western blotting. β-Actin was used as an internal control. *p < 0.05, **p < 0.01