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TAM receptors, Phosphatidylserine, inflammation, and Cancer
ABSTRACT: The numerous and diverse biological roles of Phosphatidylserine (PtdSer) are featured in this special issue. This review will focus on PtdSer as a cofactor required for stimulating TYRO3, AXL and MERTK – comprising the TAM family of receptor tyrosine kinases by their ligands Protein S (PRO...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6881992/ https://www.ncbi.nlm.nih.gov/pubmed/31775787 http://dx.doi.org/10.1186/s12964-019-0461-0 |
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author | Burstyn-Cohen, Tal Maimon, Avi |
author_facet | Burstyn-Cohen, Tal Maimon, Avi |
author_sort | Burstyn-Cohen, Tal |
collection | PubMed |
description | ABSTRACT: The numerous and diverse biological roles of Phosphatidylserine (PtdSer) are featured in this special issue. This review will focus on PtdSer as a cofactor required for stimulating TYRO3, AXL and MERTK – comprising the TAM family of receptor tyrosine kinases by their ligands Protein S (PROS1) and growth-arrest-specific 6 (GAS6) in inflammation and cancer. As PtdSer binding to TAMs is a requirement for their activation, the biological repertoire of PtdSer is now recognized to be broadened to include functions performed by TAMs. These include key homeostatic roles necessary for preserving a healthy steady state in different tissues, controlling inflammation and further additional roles in diseased states and cancer. The impact of PtdSer on inflammation and cancer through TAM signaling is a highly dynamic field of research. This review will focus on PtdSer as a necessary component of the TAM receptor-ligand complex, and for maximal TAM signaling. In particular, interactions between tumor cells and their immediate environment - the tumor microenvironment (TME) are highlighted, as both cancer cells and TME express TAMs and secrete their ligands, providing a nexus for a multifold of cross-signaling pathways which affects both immune cells and inflammation as well as tumor cell biology and growth. Here, we will highlight the current and emerging knowledge on the implications of PtdSer on TAM signaling, inflammation and cancer. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-6881992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68819922019-12-03 TAM receptors, Phosphatidylserine, inflammation, and Cancer Burstyn-Cohen, Tal Maimon, Avi Cell Commun Signal Review ABSTRACT: The numerous and diverse biological roles of Phosphatidylserine (PtdSer) are featured in this special issue. This review will focus on PtdSer as a cofactor required for stimulating TYRO3, AXL and MERTK – comprising the TAM family of receptor tyrosine kinases by their ligands Protein S (PROS1) and growth-arrest-specific 6 (GAS6) in inflammation and cancer. As PtdSer binding to TAMs is a requirement for their activation, the biological repertoire of PtdSer is now recognized to be broadened to include functions performed by TAMs. These include key homeostatic roles necessary for preserving a healthy steady state in different tissues, controlling inflammation and further additional roles in diseased states and cancer. The impact of PtdSer on inflammation and cancer through TAM signaling is a highly dynamic field of research. This review will focus on PtdSer as a necessary component of the TAM receptor-ligand complex, and for maximal TAM signaling. In particular, interactions between tumor cells and their immediate environment - the tumor microenvironment (TME) are highlighted, as both cancer cells and TME express TAMs and secrete their ligands, providing a nexus for a multifold of cross-signaling pathways which affects both immune cells and inflammation as well as tumor cell biology and growth. Here, we will highlight the current and emerging knowledge on the implications of PtdSer on TAM signaling, inflammation and cancer. GRAPHICAL ABSTRACT: [Image: see text] BioMed Central 2019-11-27 /pmc/articles/PMC6881992/ /pubmed/31775787 http://dx.doi.org/10.1186/s12964-019-0461-0 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Burstyn-Cohen, Tal Maimon, Avi TAM receptors, Phosphatidylserine, inflammation, and Cancer |
title | TAM receptors, Phosphatidylserine, inflammation, and Cancer |
title_full | TAM receptors, Phosphatidylserine, inflammation, and Cancer |
title_fullStr | TAM receptors, Phosphatidylserine, inflammation, and Cancer |
title_full_unstemmed | TAM receptors, Phosphatidylserine, inflammation, and Cancer |
title_short | TAM receptors, Phosphatidylserine, inflammation, and Cancer |
title_sort | tam receptors, phosphatidylserine, inflammation, and cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6881992/ https://www.ncbi.nlm.nih.gov/pubmed/31775787 http://dx.doi.org/10.1186/s12964-019-0461-0 |
work_keys_str_mv | AT burstyncohental tamreceptorsphosphatidylserineinflammationandcancer AT maimonavi tamreceptorsphosphatidylserineinflammationandcancer |