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Molecular Pathogenesis of Cholangiocarcinoma

Epidemiological data from the last years show an increasing trend of incidence and mortality of cholangiocarcinoma (CC) worldwide. Many pathophysiologic aspects of this neoplasia are still unknown and need to be fully discovered. However, several progresses were recently made in order to establish t...

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Detalles Bibliográficos
Autores principales: Fava, G., Lorenzini, I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Access to Research 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3169310/
https://www.ncbi.nlm.nih.gov/pubmed/21994887
http://dx.doi.org/10.1155/2012/630543
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author Fava, G.
Lorenzini, I.
author_facet Fava, G.
Lorenzini, I.
author_sort Fava, G.
collection PubMed
description Epidemiological data from the last years show an increasing trend of incidence and mortality of cholangiocarcinoma (CC) worldwide. Many pathophysiologic aspects of this neoplasia are still unknown and need to be fully discovered. However, several progresses were recently made in order to establish the molecular mechanisms involved in the transformation and growth of malignant cholangiocytes. The principal concept that at least seems to be established is that cholangiocarcinogenesis is a multistep cellular process evolving from a normal condition of the epithelial biliary cells through a chronic inflammation status ending with malignant transformation. The bad prognosis related to CC justifies why a better identification of the molecular mechanisms involved in the growth and progression of this cancer is required for the development of effective preventive measures and valid treatment regimens. This Paper describes the scientific progresses made in the last years in defining the molecular pathways implicated in the generation of this devastating disease.
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spelling pubmed-31693102011-10-12 Molecular Pathogenesis of Cholangiocarcinoma Fava, G. Lorenzini, I. Int J Hepatol Review Article Epidemiological data from the last years show an increasing trend of incidence and mortality of cholangiocarcinoma (CC) worldwide. Many pathophysiologic aspects of this neoplasia are still unknown and need to be fully discovered. However, several progresses were recently made in order to establish the molecular mechanisms involved in the transformation and growth of malignant cholangiocytes. The principal concept that at least seems to be established is that cholangiocarcinogenesis is a multistep cellular process evolving from a normal condition of the epithelial biliary cells through a chronic inflammation status ending with malignant transformation. The bad prognosis related to CC justifies why a better identification of the molecular mechanisms involved in the growth and progression of this cancer is required for the development of effective preventive measures and valid treatment regimens. This Paper describes the scientific progresses made in the last years in defining the molecular pathways implicated in the generation of this devastating disease. Hindawi Access to Research 2012 2011-07-21 /pmc/articles/PMC3169310/ /pubmed/21994887 http://dx.doi.org/10.1155/2012/630543 Text en Copyright © 2012 G. Fava and I. Lorenzini. 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 Review Article
Fava, G.
Lorenzini, I.
Molecular Pathogenesis of Cholangiocarcinoma
title Molecular Pathogenesis of Cholangiocarcinoma
title_full Molecular Pathogenesis of Cholangiocarcinoma
title_fullStr Molecular Pathogenesis of Cholangiocarcinoma
title_full_unstemmed Molecular Pathogenesis of Cholangiocarcinoma
title_short Molecular Pathogenesis of Cholangiocarcinoma
title_sort molecular pathogenesis of cholangiocarcinoma
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3169310/
https://www.ncbi.nlm.nih.gov/pubmed/21994887
http://dx.doi.org/10.1155/2012/630543
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