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METTL3 knockdown suppresses the proliferation of DLBCL cells. qRT-PCR (A) and western blotting (B) were used to assess the efficacy of METTL3 silencing in SU-DHL4 and HBL1 cells, respectively. ∗∗P < 0.01. The viability of the DLBCL cells was determined using CCK8 (C) and MTT (D) assays. (E) The cell cycle distribution of the DLBCL cells was detected by flow cytometry. ∗P < 0.05. (F) Apoptosis in SU-DHL4 and HBL1 cells was examined by using Annexin V assay. ∗P < 0.05.
