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Ursodeoxycholic Acid Influences the Expression of p27(kip1) but Not FoxO1 in Patients with Non-Cirrhotic Primary Biliary Cirrhosis

Background. Enhanced expression of cell cycle inhibitor p27(kip1) suppresses cell proliferation. Ursodeoxycholic acid (UDCA) delays progression of primary biliary cirrhosis (PBC) but its effect on p27(kip1) expression is uncertain. Aims. To analyze the expression of p27(kip1) and its transcription m...

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Autores principales: Milkiewicz, Malgorzata, Kopycińska, Justyna, Kempińska-Podhorodecka, Agnieszka, Haas, Tara, Bogdanos, Dimitrios P., Elias, Elwyn, Milkiewicz, Piotr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3987973/
https://www.ncbi.nlm.nih.gov/pubmed/24741631
http://dx.doi.org/10.1155/2014/921285
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author Milkiewicz, Malgorzata
Kopycińska, Justyna
Kempińska-Podhorodecka, Agnieszka
Haas, Tara
Bogdanos, Dimitrios P.
Elias, Elwyn
Milkiewicz, Piotr
author_facet Milkiewicz, Malgorzata
Kopycińska, Justyna
Kempińska-Podhorodecka, Agnieszka
Haas, Tara
Bogdanos, Dimitrios P.
Elias, Elwyn
Milkiewicz, Piotr
author_sort Milkiewicz, Malgorzata
collection PubMed
description Background. Enhanced expression of cell cycle inhibitor p27(kip1) suppresses cell proliferation. Ursodeoxycholic acid (UDCA) delays progression of primary biliary cirrhosis (PBC) but its effect on p27(kip1) expression is uncertain. Aims. To analyze the expression of p27(kip1) and 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. p27(kip1) expression 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; both P < 0.05 versus control). UDCA-treated non-cirrhotic patients with PBC showed decreased expression of p27(kip1) mRNA. Conclusion. PBC progression is characterized by a FoxO1-independent increase of p27(kip1) expression. In early PBC, UDCA may enhance liver regeneration via p27(kip1)-dependent mechanism.
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spelling pubmed-39879732014-04-16 Ursodeoxycholic Acid Influences the Expression of p27(kip1) but Not FoxO1 in Patients with Non-Cirrhotic Primary Biliary Cirrhosis Milkiewicz, Malgorzata Kopycińska, Justyna Kempińska-Podhorodecka, Agnieszka Haas, Tara Bogdanos, Dimitrios P. Elias, Elwyn Milkiewicz, Piotr J Immunol Res Research Article Background. Enhanced expression of cell cycle inhibitor p27(kip1) suppresses cell proliferation. Ursodeoxycholic acid (UDCA) delays progression of primary biliary cirrhosis (PBC) but its effect on p27(kip1) expression is uncertain. Aims. To analyze the expression of p27(kip1) and 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. p27(kip1) expression 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; both P < 0.05 versus control). UDCA-treated non-cirrhotic patients with PBC showed decreased expression of p27(kip1) mRNA. Conclusion. PBC progression is characterized by a FoxO1-independent increase of p27(kip1) expression. In early PBC, UDCA may enhance liver regeneration via p27(kip1)-dependent mechanism. Hindawi Publishing Corporation 2014 2014-02-05 /pmc/articles/PMC3987973/ /pubmed/24741631 http://dx.doi.org/10.1155/2014/921285 Text en Copyright © 2014 Malgorzata Milkiewicz et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Milkiewicz, Malgorzata
Kopycińska, Justyna
Kempińska-Podhorodecka, Agnieszka
Haas, Tara
Bogdanos, Dimitrios P.
Elias, Elwyn
Milkiewicz, Piotr
Ursodeoxycholic Acid Influences the Expression of p27(kip1) but Not FoxO1 in Patients with Non-Cirrhotic Primary Biliary Cirrhosis
title Ursodeoxycholic Acid Influences the Expression of p27(kip1) but Not FoxO1 in Patients with Non-Cirrhotic Primary Biliary Cirrhosis
title_full Ursodeoxycholic Acid Influences the Expression of p27(kip1) but Not FoxO1 in Patients with Non-Cirrhotic Primary Biliary Cirrhosis
title_fullStr Ursodeoxycholic Acid Influences the Expression of p27(kip1) but Not FoxO1 in Patients with Non-Cirrhotic Primary Biliary Cirrhosis
title_full_unstemmed Ursodeoxycholic Acid Influences the Expression of p27(kip1) but Not FoxO1 in Patients with Non-Cirrhotic Primary Biliary Cirrhosis
title_short Ursodeoxycholic Acid Influences the Expression of p27(kip1) but Not FoxO1 in Patients with Non-Cirrhotic Primary Biliary Cirrhosis
title_sort ursodeoxycholic acid influences the expression of p27(kip1) but not foxo1 in patients with non-cirrhotic primary biliary cirrhosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3987973/
https://www.ncbi.nlm.nih.gov/pubmed/24741631
http://dx.doi.org/10.1155/2014/921285
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