Ursodeoxycholic Acid Influences the Expression ofp27kip1but Not FoxO1 in Patients with Non-Cirrhotic Primary Biliary Cirrhosis

Abstract

Background. Enhanced expression of cell cycle inhibitorp27kip1suppresses cell proliferation. Ursodeoxycholic acid (UDCA) delays progression of primary biliary cirrhosis (PBC) but its effect onp27kip1expression is uncertain.Aims. To analyze the expression ofp27kip1and its transcription modulator FoxO1 in patients with PBC, and to assess the impact of UDCA on this pathway.Materials and Methods. The examined human tissue included explanted livers from patients with cirrhotic PBC (n=23), primary sclerosing cholangitis (PSC;n=9), alcoholic liver disease (ALD;n=9), and routine liver biopsies from patients with non-cirrhotic PBC (n=26). Healthy liver samples served as controls (n=19). Livers of FoxO-deficient mice were also studied. mRNA and protein expressions were analyzed by real-time PCR and Western blot.Results.p27kip1expression was increased in cirrhotic and non-cirrhotic PBC. FoxO1 mRNA levels were increased in PBC (8.5-fold increase versus controls). FoxO1 protein expression in PBC was comparable to controls, but it was decreased in patients with PSC and ALD (63% and 70% reduction, respectively; bothP<0.05versus control). UDCA-treated non-cirrhotic patients with PBC showed decreased expression ofp27kip1mRNA.Conclusion. PBC progression is characterized by a FoxO1-independent increase ofp27kip1expression. In early PBC, UDCA may enhance liver regeneration viap27kip1-dependent mechanism.