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Therapeutic Targeting of the Gas6/Axl Signaling Pathway in Cancer

Many signaling pathways are dysregulated in cancer cells and the host tumor microenvironment. Aberrant receptor tyrosine kinase (RTK) pathways promote cancer development, progression, and metastasis. Hence, numerous therapeutic interventions targeting RTKs have been actively pursued. Axl is an RTK t...

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Detalles Bibliográficos
Autores principales: Tanaka, Mai, Siemann, Dietmar W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469858/
https://www.ncbi.nlm.nih.gov/pubmed/34576116
http://dx.doi.org/10.3390/ijms22189953
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author Tanaka, Mai
Siemann, Dietmar W.
author_facet Tanaka, Mai
Siemann, Dietmar W.
author_sort Tanaka, Mai
collection PubMed
description Many signaling pathways are dysregulated in cancer cells and the host tumor microenvironment. Aberrant receptor tyrosine kinase (RTK) pathways promote cancer development, progression, and metastasis. Hence, numerous therapeutic interventions targeting RTKs have been actively pursued. Axl is an RTK that belongs to the Tyro3, Axl, MerTK (TAM) subfamily. Axl binds to a high affinity ligand growth arrest specific 6 (Gas6) that belongs to the vitamin K-dependent family of proteins. The Gas6/Axl signaling pathway has been implicated to promote progression, metastasis, immune evasion, and therapeutic resistance in many cancer types. Therapeutic agents targeting Gas6 and Axl have been developed, and promising results have been observed in both preclinical and clinical settings when such agents are used alone or in combination therapy. This review examines the current state of therapeutics targeting the Gas6/Axl pathway in cancer and discusses Gas6- and Axl-targeting agents that have been evaluated preclinically and clinically.
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spelling pubmed-84698582021-09-27 Therapeutic Targeting of the Gas6/Axl Signaling Pathway in Cancer Tanaka, Mai Siemann, Dietmar W. Int J Mol Sci Review Many signaling pathways are dysregulated in cancer cells and the host tumor microenvironment. Aberrant receptor tyrosine kinase (RTK) pathways promote cancer development, progression, and metastasis. Hence, numerous therapeutic interventions targeting RTKs have been actively pursued. Axl is an RTK that belongs to the Tyro3, Axl, MerTK (TAM) subfamily. Axl binds to a high affinity ligand growth arrest specific 6 (Gas6) that belongs to the vitamin K-dependent family of proteins. The Gas6/Axl signaling pathway has been implicated to promote progression, metastasis, immune evasion, and therapeutic resistance in many cancer types. Therapeutic agents targeting Gas6 and Axl have been developed, and promising results have been observed in both preclinical and clinical settings when such agents are used alone or in combination therapy. This review examines the current state of therapeutics targeting the Gas6/Axl pathway in cancer and discusses Gas6- and Axl-targeting agents that have been evaluated preclinically and clinically. MDPI 2021-09-15 /pmc/articles/PMC8469858/ /pubmed/34576116 http://dx.doi.org/10.3390/ijms22189953 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Tanaka, Mai
Siemann, Dietmar W.
Therapeutic Targeting of the Gas6/Axl Signaling Pathway in Cancer
title Therapeutic Targeting of the Gas6/Axl Signaling Pathway in Cancer
title_full Therapeutic Targeting of the Gas6/Axl Signaling Pathway in Cancer
title_fullStr Therapeutic Targeting of the Gas6/Axl Signaling Pathway in Cancer
title_full_unstemmed Therapeutic Targeting of the Gas6/Axl Signaling Pathway in Cancer
title_short Therapeutic Targeting of the Gas6/Axl Signaling Pathway in Cancer
title_sort therapeutic targeting of the gas6/axl signaling pathway in cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469858/
https://www.ncbi.nlm.nih.gov/pubmed/34576116
http://dx.doi.org/10.3390/ijms22189953
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