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AXL kinase as a novel target for cancer therapy

The AXL receptor tyrosine kinase and its major ligand, GAS6 have been demonstrated to be overexpressed and activated in many human cancers (such as lung, breast, and pancreatic cancer) and have been correlated with poor prognosis, promotion of increased invasiveness/metastasis, the EMT phenotype and...

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Autores principales: Wu, Xiaoliang, Liu, Xuewen, Koul, Sanjay, Lee, Chang Youl, Zhang, Zhenfeng, Halmos, Balazs
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4259419/
https://www.ncbi.nlm.nih.gov/pubmed/25337673
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author Wu, Xiaoliang
Liu, Xuewen
Koul, Sanjay
Lee, Chang Youl
Zhang, Zhenfeng
Halmos, Balazs
author_facet Wu, Xiaoliang
Liu, Xuewen
Koul, Sanjay
Lee, Chang Youl
Zhang, Zhenfeng
Halmos, Balazs
author_sort Wu, Xiaoliang
collection PubMed
description The AXL receptor tyrosine kinase and its major ligand, GAS6 have been demonstrated to be overexpressed and activated in many human cancers (such as lung, breast, and pancreatic cancer) and have been correlated with poor prognosis, promotion of increased invasiveness/metastasis, the EMT phenotype and drug resistance. Targeting AXL in different model systems with specific small molecule kinase inhibitors or antibodies alone or in combination with other drugs can lead to inactivation of AXL-mediated signaling pathways and can lead to regained drug sensitivity and improved therapeutic efficacy, defining AXL as a promising novel target for cancer therapeutics. This review highlights the data supporting AXL as a novel treatment candidate in a variety of cancers as well as the current status of drug development targeting the AXL/GAS6 axis and future perspectives in this emerging field.
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spelling pubmed-42594192014-12-10 AXL kinase as a novel target for cancer therapy Wu, Xiaoliang Liu, Xuewen Koul, Sanjay Lee, Chang Youl Zhang, Zhenfeng Halmos, Balazs Oncotarget Review The AXL receptor tyrosine kinase and its major ligand, GAS6 have been demonstrated to be overexpressed and activated in many human cancers (such as lung, breast, and pancreatic cancer) and have been correlated with poor prognosis, promotion of increased invasiveness/metastasis, the EMT phenotype and drug resistance. Targeting AXL in different model systems with specific small molecule kinase inhibitors or antibodies alone or in combination with other drugs can lead to inactivation of AXL-mediated signaling pathways and can lead to regained drug sensitivity and improved therapeutic efficacy, defining AXL as a promising novel target for cancer therapeutics. This review highlights the data supporting AXL as a novel treatment candidate in a variety of cancers as well as the current status of drug development targeting the AXL/GAS6 axis and future perspectives in this emerging field. Impact Journals LLC 2014-10-16 /pmc/articles/PMC4259419/ /pubmed/25337673 Text en Copyright: © 2014 Wu et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
spellingShingle Review
Wu, Xiaoliang
Liu, Xuewen
Koul, Sanjay
Lee, Chang Youl
Zhang, Zhenfeng
Halmos, Balazs
AXL kinase as a novel target for cancer therapy
title AXL kinase as a novel target for cancer therapy
title_full AXL kinase as a novel target for cancer therapy
title_fullStr AXL kinase as a novel target for cancer therapy
title_full_unstemmed AXL kinase as a novel target for cancer therapy
title_short AXL kinase as a novel target for cancer therapy
title_sort axl kinase as a novel target for cancer therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4259419/
https://www.ncbi.nlm.nih.gov/pubmed/25337673
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