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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Main Authors: Dan Yan, H. Shelton Earp, Deborah DeRyckere, Douglas K. Graham
Format: Article
Language:English
Published: MDPI AG 2021-11-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/13/22/5639
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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
collection DOAJ
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.
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spelling doaj.art-f008783afb8b4deca24ca6395ea261cc2023-11-22T22:41:08ZengMDPI AGCancers2072-66942021-11-011322563910.3390/cancers13225639Targeting MERTK and AXL in <i>EGFR</i> Mutant Non-Small Cell Lung CancerDan Yan0H. Shelton Earp1Deborah DeRyckere2Douglas K. Graham3Aflac Cancer and Blood Disorders Center, Children’s Healthcare of Atlanta, Department of Pediatrics, Emory University, Atlanta, GA 30322, USAUNC Lineberger Comprehensive Cancer Center, Department of Medicine, Chapel Hill, NC 27599, USAAflac Cancer and Blood Disorders Center, Children’s Healthcare of Atlanta, Department of Pediatrics, Emory University, Atlanta, GA 30322, USAAflac Cancer and Blood Disorders Center, Children’s Healthcare of Atlanta, Department of Pediatrics, Emory University, Atlanta, GA 30322, USAMERTK 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.https://www.mdpi.com/2072-6694/13/22/5639MERTKAXLTAM familyreceptor tyrosine kinasetargeted therapyNSCLC
spellingShingle Dan Yan
H. Shelton Earp
Deborah DeRyckere
Douglas K. Graham
Targeting MERTK and AXL in <i>EGFR</i> Mutant Non-Small Cell Lung Cancer
Cancers
MERTK
AXL
TAM family
receptor tyrosine kinase
targeted therapy
NSCLC
title 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_short 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
topic MERTK
AXL
TAM family
receptor tyrosine kinase
targeted therapy
NSCLC
url https://www.mdpi.com/2072-6694/13/22/5639
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