International Journal of Molecular and Cellular Medicine (IJMCM)

Although the antidiabetic drug metformin (MET) exhibits anticancer properties, its mechanisms of action in prostate and liver cancer remain unclear. This study aimed to investigate the antiproliferative effects of MET and its impact on key regulatory genes involved in the Wnt, one-carbon metabolism, and p53 signaling pathways in prostate (PC3) and liver (HepG2) cancer cells. Bioinformatic analysis of public RNA-seq datasets (C4-2 and Huh-7) was performed to identify differentially expressed genes following MET exposure. DKK1, MTHFD2, and GADD45A were selected for validation. PC3 and HepG2 cells were treated with MET (5–40 mM) for 24 hours. Cell viability was evaluated using the CCK-8 assay, and RT-qPCR was employed to quantify changes in gene expression.MET inhibited the proliferation of both cell lines in a dose-dependent manner. In MET-treated PC3 cells, DKK1 expression increased up to 2.08-fold, but decreased to 0.6-fold in HepG2 cells. MTHFD2 expression rose in both lines. GADD45A expression was consistently elevated.These results demonstrate that MET has a significant antiproliferative effect on prostate and liver cancer cells. The differential regulation of DKK1 and MTHFD2, along with the consistent upregulation of GADD45A, is associated with MET's antitumor activity. Although this study did not directly test the exact mechanistic causality, the findings suggest that these pathways may play essential roles in MET's action, particularly the activation of the p53 pathway through GADD45A. This study identifies key molecular associations and supports further investigation into MET's therapeutic potential by exploring these altered oncogenic pathways.