The functional role of integrins during intra- and extravasation within the metastatic cascade

Abstract Formation of distant metastases is by far the most common cause of cancer-related deaths. The process of metastasis formation is complex, and within this complex process the formation of migratory cells, the so called epithelial mesenchymal transition (EMT), which enables cancer cells to br...

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Main Authors: Greta Sökeland, Udo Schumacher
Format: Article
Language:English
Published: BMC 2019-01-01
Series:Molecular Cancer
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12943-018-0937-3
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author Greta Sökeland
Udo Schumacher
author_facet Greta Sökeland
Udo Schumacher
author_sort Greta Sökeland
collection DOAJ
description Abstract Formation of distant metastases is by far the most common cause of cancer-related deaths. The process of metastasis formation is complex, and within this complex process the formation of migratory cells, the so called epithelial mesenchymal transition (EMT), which enables cancer cells to break loose from the primary tumor mass and to enter the bloodstream, is of particular importance. To break loose from the primary cancer, cancer cells have to down-regulate the cell-to-cell adhesion molecuIes (CAMs) which keep them attached to neighboring cancer cells. In contrast to this downregulation of CAMS in the primary tumor, cancer cells up-regulate other types of CAMs, that enable them to attach to the endothelium in the organ of the future metastasis. During EMT, the expression of cell-to-cell and cell-to-matrix adhesion molecules and their down- and upregulation is therefore critical for metastasis formation. Tumor cells mimic leukocytes to enable transmigration of the endothelial barrier at the metastatic site. The attachment of leukocytes/cancer cells to the endothelium are mediated by several CAMs different from those at the site of the primary tumor. These CAMs and their ligands are organized in a sequential row, the leukocyte adhesion cascade. In this adhesion process, integrins and their ligands are centrally involved in the molecular interactions governing the transmigration. This review discusses the integrin expression patterns found on primary tumor cells and studies whether their expression correlates with tumor progression, metastatic capacity and prognosis. Simultaneously, further possible, but so far unclearly characterized, alternative adhesion molecules and/or ligands, will be considered and emerging therapeutic possibilities reviewed.
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spelling doaj.art-44599e5e9dae49b2b25d5c35681e9b8b2022-12-22T03:38:30ZengBMCMolecular Cancer1476-45982019-01-0118111910.1186/s12943-018-0937-3The functional role of integrins during intra- and extravasation within the metastatic cascadeGreta Sökeland0Udo Schumacher1Institute of Anatomy and Experimental Morphology, University Cancer Center, University Medical Center Hamburg EppendorfInstitute of Anatomy and Experimental Morphology, University Cancer Center, University Medical Center Hamburg EppendorfAbstract Formation of distant metastases is by far the most common cause of cancer-related deaths. The process of metastasis formation is complex, and within this complex process the formation of migratory cells, the so called epithelial mesenchymal transition (EMT), which enables cancer cells to break loose from the primary tumor mass and to enter the bloodstream, is of particular importance. To break loose from the primary cancer, cancer cells have to down-regulate the cell-to-cell adhesion molecuIes (CAMs) which keep them attached to neighboring cancer cells. In contrast to this downregulation of CAMS in the primary tumor, cancer cells up-regulate other types of CAMs, that enable them to attach to the endothelium in the organ of the future metastasis. During EMT, the expression of cell-to-cell and cell-to-matrix adhesion molecules and their down- and upregulation is therefore critical for metastasis formation. Tumor cells mimic leukocytes to enable transmigration of the endothelial barrier at the metastatic site. The attachment of leukocytes/cancer cells to the endothelium are mediated by several CAMs different from those at the site of the primary tumor. These CAMs and their ligands are organized in a sequential row, the leukocyte adhesion cascade. In this adhesion process, integrins and their ligands are centrally involved in the molecular interactions governing the transmigration. This review discusses the integrin expression patterns found on primary tumor cells and studies whether their expression correlates with tumor progression, metastatic capacity and prognosis. Simultaneously, further possible, but so far unclearly characterized, alternative adhesion molecules and/or ligands, will be considered and emerging therapeutic possibilities reviewed.http://link.springer.com/article/10.1186/s12943-018-0937-3CancerEpithelial mesenchymal transitionSelectinIntegrinIntegrin ligandsLeukocyte adhesion cascade
spellingShingle Greta Sökeland
Udo Schumacher
The functional role of integrins during intra- and extravasation within the metastatic cascade
Molecular Cancer
Cancer
Epithelial mesenchymal transition
Selectin
Integrin
Integrin ligands
Leukocyte adhesion cascade
title The functional role of integrins during intra- and extravasation within the metastatic cascade
title_full The functional role of integrins during intra- and extravasation within the metastatic cascade
title_fullStr The functional role of integrins during intra- and extravasation within the metastatic cascade
title_full_unstemmed The functional role of integrins during intra- and extravasation within the metastatic cascade
title_short The functional role of integrins during intra- and extravasation within the metastatic cascade
title_sort functional role of integrins during intra and extravasation within the metastatic cascade
topic Cancer
Epithelial mesenchymal transition
Selectin
Integrin
Integrin ligands
Leukocyte adhesion cascade
url http://link.springer.com/article/10.1186/s12943-018-0937-3
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