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PMID: 15918149 Published · ppublish English Journal Article Review

Hepatocellular carcinoma: molecular pathways and new therapeutic targets.

Seminars in liver disease ·Vol. 25 ·No. 2 ·2005-00-00 ·Pages 212-25

Roberts LR, Gores GJ

Abstract

Hepatocellular carcinoma is often diagnosed at an advanced stage, when it is not amenable to curative therapies. There is no effective chemotherapy. Advances in cancer biology suggest that a limited number of pathways are responsible for initiating and maintaining dysregulated cell proliferation, which is the major cellular alteration responsible for the cancer phenotype. New treatments in development target several of these critical pathways, including agents targeting the receptor tyrosine kinase pathways, the Wnt/beta-catenin signaling pathway, the ubiquitin/proteasome degradation pathway, the epigenetic DNA methylation and histone deacetylation pathways, the PI3 kinase/AKT/mTOR pathway, angiogenic pathways, and telomerase. Several of these approaches hold significant promise for improving the long-term outcome of patients with advanced hepatocellular carcinoma. Because of the high prevalence of liver cirrhosis in hepatocellular carcinoma patients, these approaches must be coupled with new strategies for halting or reversing the progression of chronic liver disease.

MeSH Terms
Animals Carcinoma, Hepatocellular/drug therapy,pathology,physiopathology Cell Transformation, Neoplastic DNA Methylation Disease Models, Animal Homeostasis/physiology Humans Liver Neoplasms/drug therapy,pathology,physiopathology Phosphatidylinositol 3-Kinases/metabolism Protein Serine-Threonine Kinases/metabolism,physiology Proto-Oncogene Proteins/metabolism Proto-Oncogene Proteins c-akt Receptor Protein-Tyrosine Kinases/antagonists & inhibitors,physiology Receptors, Vascular Endothelial Growth Factor/physiology Signal Transduction/drug effects,physiology
Chemicals
Proto-Oncogene Proteins Receptor Protein-Tyrosine Kinases Receptors, Vascular Endothelial Growth Factor AKT1 protein, human Protein Serine-Threonine Kinases Proto-Oncogene Proteins c-akt NF-kappa B kinase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Roberts Lewis R
Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, Rochester, Minnesota 55902, USA.
Gores Gregory J
Article Info
Journal
Seminars in liver disease
Abbr.
Semin Liver Dis
ISSN
0272-8087
Published
2005-00-00
Pages
212-25
Language
English
Region
United States
NLM ID
8110297
Subset
IM
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