miR-34c inhibited Dicer/Pten DKO
cancer cell growth by inducing cell cycle arrest in G1 phase and apoptosis.
Dicer/Pten cancer cell lines were transfected with
mmu-miR-34c, mmu-let-7b, or miRNA mimic negative
control using Lipofectamine RNAiMAX. After 2 days, viability of treated
Dicer/Pten DKO cancer cells was measured by
Promega CellTiter-Glo assay (A). Representative cell cycle profile of
miR-34c-treated cells was determined by flow cytometry using PI
staining and analyzed by flowjo software (B). Caspase activities of
miR-34c-treated DKO-1 were measured by Promega caspase-Glo 3/7
assay (C). Data of cell viability, cell cycle profile, and caspase
activity are expressed as mean values ± SEM for three determinations
(*P < 0.05).