Cargando…

Clinical Development of c-MET Inhibition in Hepatocellular Carcinoma

Hepatocellular carcinoma (HCC) is one of the leading causes of cancer death. In patients with advanced or unresectable HCC, there are few treatment options. Conventional chemotherapy has limited benefits. Sorafenib, a multi-kinase inhibitor, improves survival, but options for patients intolerant of...

Descripción completa

Detalles Bibliográficos
Autores principales: Lee, Joycelyn J. X., Chan, Jack J., Choo, Su Pin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548260/
https://www.ncbi.nlm.nih.gov/pubmed/28943627
http://dx.doi.org/10.3390/diseases3040306
_version_ 1783255810237792256
author Lee, Joycelyn J. X.
Chan, Jack J.
Choo, Su Pin
author_facet Lee, Joycelyn J. X.
Chan, Jack J.
Choo, Su Pin
author_sort Lee, Joycelyn J. X.
collection PubMed
description Hepatocellular carcinoma (HCC) is one of the leading causes of cancer death. In patients with advanced or unresectable HCC, there are few treatment options. Conventional chemotherapy has limited benefits. Sorafenib, a multi-kinase inhibitor, improves survival, but options for patients intolerant of or progressing on sorafenib are limited. There has been much interest in recent years in molecular therapeutic targets and drug development for HCC. One of the more promising molecular targets in HCC is the cellular-mesenchymal-epithelial transition (c-MET) factor receptor. Encouraging phase II data on two c-MET inhibitors, tivantinib and cabozantinib, has led to phase III trials. This review describes the c-MET/hepatocyte growth factor (HGF) signalling pathway and its relevance to HCC, and discusses the preclinical and clinical trial data for inhibitors of this pathway in HCC.
format Online
Article
Text
id pubmed-5548260
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-55482602017-09-12 Clinical Development of c-MET Inhibition in Hepatocellular Carcinoma Lee, Joycelyn J. X. Chan, Jack J. Choo, Su Pin Diseases Review Hepatocellular carcinoma (HCC) is one of the leading causes of cancer death. In patients with advanced or unresectable HCC, there are few treatment options. Conventional chemotherapy has limited benefits. Sorafenib, a multi-kinase inhibitor, improves survival, but options for patients intolerant of or progressing on sorafenib are limited. There has been much interest in recent years in molecular therapeutic targets and drug development for HCC. One of the more promising molecular targets in HCC is the cellular-mesenchymal-epithelial transition (c-MET) factor receptor. Encouraging phase II data on two c-MET inhibitors, tivantinib and cabozantinib, has led to phase III trials. This review describes the c-MET/hepatocyte growth factor (HGF) signalling pathway and its relevance to HCC, and discusses the preclinical and clinical trial data for inhibitors of this pathway in HCC. MDPI 2015-10-28 /pmc/articles/PMC5548260/ /pubmed/28943627 http://dx.doi.org/10.3390/diseases3040306 Text en © 2015 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Lee, Joycelyn J. X.
Chan, Jack J.
Choo, Su Pin
Clinical Development of c-MET Inhibition in Hepatocellular Carcinoma
title Clinical Development of c-MET Inhibition in Hepatocellular Carcinoma
title_full Clinical Development of c-MET Inhibition in Hepatocellular Carcinoma
title_fullStr Clinical Development of c-MET Inhibition in Hepatocellular Carcinoma
title_full_unstemmed Clinical Development of c-MET Inhibition in Hepatocellular Carcinoma
title_short Clinical Development of c-MET Inhibition in Hepatocellular Carcinoma
title_sort clinical development of c-met inhibition in hepatocellular carcinoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548260/
https://www.ncbi.nlm.nih.gov/pubmed/28943627
http://dx.doi.org/10.3390/diseases3040306
work_keys_str_mv AT leejoycelynjx clinicaldevelopmentofcmetinhibitioninhepatocellularcarcinoma
AT chanjackj clinicaldevelopmentofcmetinhibitioninhepatocellularcarcinoma
AT choosupin clinicaldevelopmentofcmetinhibitioninhepatocellularcarcinoma