Targeting MERTK and AXL in <i>EGFR</i> Mutant Non-Small Cell Lung Cancer
MERTK and AXL are members of the TAM family of receptor tyrosine kinases and are abnormally expressed in 69% and 93% of non-small cell lung cancers (NSCLCs), respectively. Expression of MERTK and/or AXL provides a survival advantage for NSCLC cells and correlates with lymph node metastasis, drug res...
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MDPI AG
2021
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oai:doaj.org-article:f008783afb8b4deca24ca6395ea261cc2021-11-25T17:01:57ZTargeting MERTK and AXL in <i>EGFR</i> Mutant Non-Small Cell Lung Cancer10.3390/cancers132256392072-6694https://doaj.org/article/f008783afb8b4deca24ca6395ea261cc2021-11-01T00:00:00Zhttps://www.mdpi.com/2072-6694/13/22/5639https://doaj.org/toc/2072-6694MERTK and AXL are members of the TAM family of receptor tyrosine kinases and are abnormally expressed in 69% and 93% of non-small cell lung cancers (NSCLCs), respectively. Expression of MERTK and/or AXL provides a survival advantage for NSCLC cells and correlates with lymph node metastasis, drug resistance, and disease progression in patients with NSCLC. The TAM receptors on host tumor infiltrating cells also play important roles in the immunosuppressive tumor microenvironment. Thus, MERTK and AXL are attractive biologic targets for NSCLC treatment. Here, we will review physiologic and oncologic roles for MERTK and AXL with an emphasis on the potential to target these kinases in NSCLCs with activating EGFR mutations.Dan YanH. Shelton EarpDeborah DeRyckereDouglas K. GrahamMDPI AGarticleMERTKAXLTAM familyreceptor tyrosine kinasetargeted therapyNSCLCNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENCancers, Vol 13, Iss 5639, p 5639 (2021) |
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DOAJ |
language |
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topic |
MERTK AXL TAM family receptor tyrosine kinase targeted therapy NSCLC Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 |
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MERTK AXL TAM family receptor tyrosine kinase targeted therapy NSCLC Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 Dan Yan H. Shelton Earp Deborah DeRyckere Douglas K. Graham Targeting MERTK and AXL in <i>EGFR</i> Mutant Non-Small Cell Lung Cancer |
description |
MERTK and AXL are members of the TAM family of receptor tyrosine kinases and are abnormally expressed in 69% and 93% of non-small cell lung cancers (NSCLCs), respectively. Expression of MERTK and/or AXL provides a survival advantage for NSCLC cells and correlates with lymph node metastasis, drug resistance, and disease progression in patients with NSCLC. The TAM receptors on host tumor infiltrating cells also play important roles in the immunosuppressive tumor microenvironment. Thus, MERTK and AXL are attractive biologic targets for NSCLC treatment. Here, we will review physiologic and oncologic roles for MERTK and AXL with an emphasis on the potential to target these kinases in NSCLCs with activating EGFR mutations. |
format |
article |
author |
Dan Yan H. Shelton Earp Deborah DeRyckere Douglas K. Graham |
author_facet |
Dan Yan H. Shelton Earp Deborah DeRyckere Douglas K. Graham |
author_sort |
Dan Yan |
title |
Targeting MERTK and AXL in <i>EGFR</i> Mutant Non-Small Cell Lung Cancer |
title_short |
Targeting MERTK and AXL in <i>EGFR</i> Mutant Non-Small Cell Lung Cancer |
title_full |
Targeting MERTK and AXL in <i>EGFR</i> Mutant Non-Small Cell Lung Cancer |
title_fullStr |
Targeting MERTK and AXL in <i>EGFR</i> Mutant Non-Small Cell Lung Cancer |
title_full_unstemmed |
Targeting MERTK and AXL in <i>EGFR</i> Mutant Non-Small Cell Lung Cancer |
title_sort |
targeting mertk and axl in <i>egfr</i> mutant non-small cell lung cancer |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/f008783afb8b4deca24ca6395ea261cc |
work_keys_str_mv |
AT danyan targetingmertkandaxliniegfrimutantnonsmallcelllungcancer AT hsheltonearp targetingmertkandaxliniegfrimutantnonsmallcelllungcancer AT deborahderyckere targetingmertkandaxliniegfrimutantnonsmallcelllungcancer AT douglaskgraham targetingmertkandaxliniegfrimutantnonsmallcelllungcancer |
_version_ |
1718412811913134080 |