Altered Cell Adhesion and Glycosylation Promote Cancer Immune Suppression and Metastasis

Cell-cell interactions and cell adhesion are key mediators of cancer progression and facilitate hallmarks of cancer including immune evasion and metastatic dissemination. Many cell adhesion molecules within the tumor microenvironment are changed and significant alterations of glycosylation are obser...

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Main Authors: Heinz Läubli, Lubor Borsig
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-09-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fimmu.2019.02120/full
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spelling doaj-3d5fc860e4f64d3b86f2998b9e1f1ccf2020-11-25T01:02:14ZengFrontiers Media S.A.Frontiers in Immunology1664-32242019-09-011010.3389/fimmu.2019.02120484841Altered Cell Adhesion and Glycosylation Promote Cancer Immune Suppression and MetastasisHeinz Läubli0Lubor Borsig1Lubor Borsig2Laboratory for Cancer Immunotherapy, Department of Biomedicine and Medical Oncology, Department of Internal Medicine, University Hospital, Basel, SwitzerlandDepartment of Physiology, University of Zurich, Zurich, SwitzerlandComprehensive Cancer Center, Zurich, SwitzerlandCell-cell interactions and cell adhesion are key mediators of cancer progression and facilitate hallmarks of cancer including immune evasion and metastatic dissemination. Many cell adhesion molecules within the tumor microenvironment are changed and significant alterations of glycosylation are observed. These changes in cell adhesion molecules alter the ability of tumor cells to interact with other cells and extracellular matrix proteins. Three families of cell-cell interaction molecules selectins, Siglecs, and integrins have been associated with cancer progression in many pre-clinical studies, yet inhibition of cell adhesion as a therapeutic target is just beginning to be explored. We review how cell-cell interactions mediated by integrins and the glycan-binding receptors selectins and Siglec receptors support cancer progression. The discussion focuses on mechanisms during immune evasion and metastasis that can be therapeutically targeted by blocking these cell-cell interactions.https://www.frontiersin.org/article/10.3389/fimmu.2019.02120/fullselectinSiglecintegrinimmunitysialic acidtumor microenvironment
collection DOAJ
language English
format Article
sources DOAJ
author Heinz Läubli
Lubor Borsig
Lubor Borsig
spellingShingle Heinz Läubli
Lubor Borsig
Lubor Borsig
Altered Cell Adhesion and Glycosylation Promote Cancer Immune Suppression and Metastasis
Frontiers in Immunology
selectin
Siglec
integrin
immunity
sialic acid
tumor microenvironment
author_facet Heinz Läubli
Lubor Borsig
Lubor Borsig
author_sort Heinz Läubli
title Altered Cell Adhesion and Glycosylation Promote Cancer Immune Suppression and Metastasis
title_short Altered Cell Adhesion and Glycosylation Promote Cancer Immune Suppression and Metastasis
title_full Altered Cell Adhesion and Glycosylation Promote Cancer Immune Suppression and Metastasis
title_fullStr Altered Cell Adhesion and Glycosylation Promote Cancer Immune Suppression and Metastasis
title_full_unstemmed Altered Cell Adhesion and Glycosylation Promote Cancer Immune Suppression and Metastasis
title_sort altered cell adhesion and glycosylation promote cancer immune suppression and metastasis
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2019-09-01
description Cell-cell interactions and cell adhesion are key mediators of cancer progression and facilitate hallmarks of cancer including immune evasion and metastatic dissemination. Many cell adhesion molecules within the tumor microenvironment are changed and significant alterations of glycosylation are observed. These changes in cell adhesion molecules alter the ability of tumor cells to interact with other cells and extracellular matrix proteins. Three families of cell-cell interaction molecules selectins, Siglecs, and integrins have been associated with cancer progression in many pre-clinical studies, yet inhibition of cell adhesion as a therapeutic target is just beginning to be explored. We review how cell-cell interactions mediated by integrins and the glycan-binding receptors selectins and Siglec receptors support cancer progression. The discussion focuses on mechanisms during immune evasion and metastasis that can be therapeutically targeted by blocking these cell-cell interactions.
topic selectin
Siglec
integrin
immunity
sialic acid
tumor microenvironment
url https://www.frontiersin.org/article/10.3389/fimmu.2019.02120/full
work_keys_str_mv AT heinzlaubli alteredcelladhesionandglycosylationpromotecancerimmunesuppressionandmetastasis
AT luborborsig alteredcelladhesionandglycosylationpromotecancerimmunesuppressionandmetastasis
AT luborborsig alteredcelladhesionandglycosylationpromotecancerimmunesuppressionandmetastasis
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