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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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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 |
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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 |
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