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dc.contributor.authorWong, C.
dc.contributor.authorDye, Danielle
dc.contributor.authorCoombe, Deirdre
dc.date.accessioned2017-01-30T12:23:05Z
dc.date.available2017-01-30T12:23:05Z
dc.date.created2012-10-25T20:00:27Z
dc.date.issued2012
dc.identifier.citationWong, Chee Wai and Dye, Danielle E. and Coombe, Deirdre R. 2012. The Role of Immunoglobulin Superfamily Cell Adhesion Molecules in Cancer Metastasis. International Journal of Cell Biology. Article ID 340296.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/21079
dc.identifier.doi10.1155/2012/340296
dc.description.abstract

Metastasis is a major clinical problem and results in a poor prognosis for most cancers. The metastatic pathway describes the process by which cancer cells give rise to a metastatic lesion in a new tissue or organ. It consists of interconnecting steps all of which must be successfully completed to result in a metastasis. Cell-cell adhesion is a key aspect of many of these steps. Adhesion molecules belonging to the immunoglobulin superfamily (Ig-SF) commonly play a central role in cell-cell adhesion, and a number of these molecules have been associated with cancer progression and a metastatic phenotype. Surprisingly, the contribution of Ig-SF members to metastasis has not received the attention afforded other cell adhesion molecules (CAMs) such as the integrins. Here we examine the steps in the metastatic pathway focusing on how the Ig-SF members, melanoma cell adhesion molecule (MCAM), L1CAM, neural CAM (NCAM), leukocyte CAM (ALCAM), intercellular CAM-1 (ICAM-1) and platelet endothelial CAM-1 (PECAM-1) could play a role. Although much remains to be understood, this review aims to raise the profile of Ig-SF members in metastasis formation and prompt further research that could lead to useful clinical outcomes.

dc.publisherHindawi Publishing Corporation
dc.subjectmetastatic lesion
dc.subjectmetastasis
dc.subjectcancer
dc.titleThe Role of Immunoglobulin Superfamily Cell Adhesion Molecules in Cancer Metastasis
dc.typeJournal Article
dcterms.source.volume2012
dcterms.source.issn1687-8876
dcterms.source.titleInternational Journal of Cell Biology
curtin.note

This article is published under the Open Access publishing model and distributed under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0/ Please refer to the licence to obtain terms for any further reuse or distribution of this work.

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curtin.accessStatusOpen access


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