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Cell adhesion and invasion during secondary tumor formation: interactions between tumor cells and host organs

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Part of the book series: Cancer Growth and Progression ((CAGP,volume 11))

Abstract

To form clinically evident metastases, the main cause of death in cancer patients, cancer cells must complete a highly complex series of steps called the metastatic cascade. This includes local invasion, intravasation, transport in the circulation, adhesion and extravasation, survival, proliferation and angiogenesis. Since failure to complete any one of these steps results in metastatic failure, understanding the steps of the metastatic cascade may allow us to develop new therapeutic approaches for the treatment of cancer. Here we review the role of specific tumor cell (TC) adhesion and migration processes in organ-selective metastases formation. TC adhesion in the microvasculature of host organs is a specific and highly regulated process. Important adhesion molecules are: selectins in TC-endothelial cell adhesion and integrins in TC–extracellular matrix interactions. Defined expression of adhesion molecules and their corresponding ligands can govern this non-random process of organ-selective metastasis formation. Once TC adhesion in the microcirculation occurs, early extravasation of TCs, which is regulated by chemotactic stimuli of growth factors and/or chemokines in an organ-specific manner, can be observed.

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Gassmann, P., Haier, J., Nicolson, G.L. (2008). Cell adhesion and invasion during secondary tumor formation: interactions between tumor cells and host organs. In: Kaiser, H.E., Nasir, A. (eds) Selected Aspects of Cancer Progression: Metastasis, Apoptosis and Immune Response. Cancer Growth and Progression, vol 11. Springer, Dordrecht. https://doi.org/10.1007/978-1-4020-6729-7_3

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