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The Dual Role of TAM Receptors in Autoimmune Diseases and Cancer: An Overview
Receptor tyrosine kinases (RTKs) regulate cellular processes by converting signals from the extracellular environment to the cytoplasm and nucleus. Tyro3, Axl, and Mer (TAM) receptors form an RTK family that plays an intricate role in tissue maintenance, phagocytosis, and inflammation as well as cel...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6210017/ https://www.ncbi.nlm.nih.gov/pubmed/30322068 http://dx.doi.org/10.3390/cells7100166 |
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author | Wium, Martha Paccez, Juliano D. Zerbini, Luiz F. |
author_facet | Wium, Martha Paccez, Juliano D. Zerbini, Luiz F. |
author_sort | Wium, Martha |
collection | PubMed |
description | Receptor tyrosine kinases (RTKs) regulate cellular processes by converting signals from the extracellular environment to the cytoplasm and nucleus. Tyro3, Axl, and Mer (TAM) receptors form an RTK family that plays an intricate role in tissue maintenance, phagocytosis, and inflammation as well as cell proliferation, survival, migration, and development. Defects in TAM signaling are associated with numerous autoimmune diseases and different types of cancers. Here, we review the structure of TAM receptors, their ligands, and their biological functions. We discuss the role of TAM receptors and soluble circulating TAM receptors in the autoimmune diseases systemic lupus erythematosus (SLE) and multiple sclerosis (MS). Lastly, we discuss the effect of TAM receptor deregulation in cancer and explore the therapeutic potential of TAM receptors in the treatment of diseases. |
format | Online Article Text |
id | pubmed-6210017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62100172018-11-02 The Dual Role of TAM Receptors in Autoimmune Diseases and Cancer: An Overview Wium, Martha Paccez, Juliano D. Zerbini, Luiz F. Cells Review Receptor tyrosine kinases (RTKs) regulate cellular processes by converting signals from the extracellular environment to the cytoplasm and nucleus. Tyro3, Axl, and Mer (TAM) receptors form an RTK family that plays an intricate role in tissue maintenance, phagocytosis, and inflammation as well as cell proliferation, survival, migration, and development. Defects in TAM signaling are associated with numerous autoimmune diseases and different types of cancers. Here, we review the structure of TAM receptors, their ligands, and their biological functions. We discuss the role of TAM receptors and soluble circulating TAM receptors in the autoimmune diseases systemic lupus erythematosus (SLE) and multiple sclerosis (MS). Lastly, we discuss the effect of TAM receptor deregulation in cancer and explore the therapeutic potential of TAM receptors in the treatment of diseases. MDPI 2018-10-12 /pmc/articles/PMC6210017/ /pubmed/30322068 http://dx.doi.org/10.3390/cells7100166 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Wium, Martha Paccez, Juliano D. Zerbini, Luiz F. The Dual Role of TAM Receptors in Autoimmune Diseases and Cancer: An Overview |
title | The Dual Role of TAM Receptors in Autoimmune Diseases and Cancer: An Overview |
title_full | The Dual Role of TAM Receptors in Autoimmune Diseases and Cancer: An Overview |
title_fullStr | The Dual Role of TAM Receptors in Autoimmune Diseases and Cancer: An Overview |
title_full_unstemmed | The Dual Role of TAM Receptors in Autoimmune Diseases and Cancer: An Overview |
title_short | The Dual Role of TAM Receptors in Autoimmune Diseases and Cancer: An Overview |
title_sort | dual role of tam receptors in autoimmune diseases and cancer: an overview |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6210017/ https://www.ncbi.nlm.nih.gov/pubmed/30322068 http://dx.doi.org/10.3390/cells7100166 |
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