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...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Dan Yan, H. Shelton Earp, Deborah DeRyckere, Douglas K. Graham
Formato: article
Lenguaje:EN
Publicado: MDPI AG 2021
Materias:
AXL
Acceso en línea:https://doaj.org/article/f008783afb8b4deca24ca6395ea261cc
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:f008783afb8b4deca24ca6395ea261cc
record_format dspace
spelling 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)
institution DOAJ
collection DOAJ
language EN
topic MERTK
AXL
TAM family
receptor tyrosine kinase
targeted therapy
NSCLC
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle 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