Figure 4.KMT2A regulated cervical cancer cell proliferation and colony formation by targeting VDAC1. Human cervical cancer Siha and Caski cells were transfected with KMT2A shRNAs or KMT2A shRNA + VDAC1 overexpression plasmid. At 48 hours after transfection, the cell viability, colony formation and migration ability were measured. (A) Viable Siha and Caski cells. (B) The average cell viability %. (C) Colony formation of Siha and Caski cells. (D) The average count numbers.
