Differential role of PTEN in transforming growth factor β (TGF‐β) effects on proliferation and migration in prostate cancer cells

摘要

Background Transforming growth factor‐β (TGF‐β) acts as a tumor suppressor in normal epithelial cells but as a tumor promoter in advanced prostate cancer cells. PI3‐kinase pathway mediates TGF‐β effects on prostate cancer cell migration and invasion. PTEN inhibits PI3‐kinase pathway and is frequently mutated in prostate cancers. We investigated possible role(s) of PTEN in TGF‐β effects on proliferation and migration in prostate cancer cells. Methods Expression of PTEN mRNA and proteins were determined using RT‐PCR and Western blotting in RWPE1 and DU145 cells. We also studied the role of PTEN in TGF‐β effects on cell proliferation and migration in DU145 cells after transient silencing of endogenous PTEN. Conversely, we determined the role of PTEN in cell proliferation and migration after over‐expression of PTEN in PC3 cells which lack endogenous PTEN. Results TGF‐β1 and TGF‐β3 had no effect on PTEN mRNA levels but both isoforms increased PTEN protein levels in DU145 and RWPE1 cells indicating that PTEN may mediate TGF‐β effects on cell proliferation. Knockdown of PTEN in DU145 cells resulted in significant increase in cell proliferation which was not affected by TGF‐β isoforms. PTEN overexpression in PC3 cells inhibited cell proliferation. Knockdown of endogenous PTEN enhanced cell migration in DU145 cells, whereas PTEN overexpression reduced migration in PC3 cells and reduced phosphorylation of AKT in response to TGF‐β. Conclusion We conclude that PTEN plays a role in inhibitory effects of TGF‐β on cell proliferation whereas its absence may enhance TGF‐β effects on activation of PI3‐kinase pathway and cell migration.