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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2014
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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. |
format | Online Article Text |
id | pubmed-4259419 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
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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