Warning: Undefined variable $zfal in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 525
Deprecated: str_replace(): Passing null to parameter #3 ($subject) of type array|string is deprecated in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 525
Warning: Undefined variable $sterm in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 530
free
Warning: Undefined variable $sterm in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 531
free free
English Wikipedia
Nephropedia Template TP (
Twit Text
DeepDyve Pubget Overpricing |
lüll Targeting insulin-like growth factor axis in hepatocellular carcinoma Wu J; Zhu AXJ Hematol Oncol 2011[Jul]; 4 (ä): 30The insulin-like growth factor (IGF) axis contains ligands, receptors, substrates, and ligand binding proteins. The essential role of IGF axis in hepatocellular carcinoma (HCC) has been illustrated in HCC cell lines and in animal xenograft models. Preclinical evidence provides ample indication that all four components of IGF axis are crucial in the carcinogenic and metastatic potential of HCC. Several strategies targeting this system including monoclonal antibodies against the IGF 1 receptor (IGF-1R) and small molecule inhibitors of the tyrosine kinase function of IGF-1R are under active investigation. This review describes the most up-to-date understanding of this complex axis in HCC, and provides relevant information on clinical trials targeting the IGF axis in HCC with a focus on anti-IGF-1R approach. IGF axis is increasingly recognized as one of the most relevant pathways in HCC and agents targeting this axis can potentially play an important role in the treatment of HCC.|Animals[MESH]|Antibodies, Monoclonal/pharmacology/therapeutic use[MESH]|Antineoplastic Agents/chemistry/pharmacology/*therapeutic use[MESH]|Carcinoma, Hepatocellular/*drug therapy/metabolism[MESH]|Humans[MESH]|Liver Neoplasms/*drug therapy/metabolism[MESH]|Protein Kinase Inhibitors/chemistry/pharmacology/therapeutic use[MESH]|Receptor, IGF Type 1/*antagonists & inhibitors/metabolism[MESH]|Small Molecule Libraries/chemistry/pharmacology/therapeutic use[MESH]|Somatomedins/*metabolism[MESH] |