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dc.contributor.authorAhmedah, H.T.*
dc.contributor.authorPatterson, Laurence H.*
dc.contributor.authorShnyder, Steven*
dc.contributor.authorSheldrake, Helen M.*
dc.date.accessioned2017-06-06T13:51:20Z
dc.date.available2017-06-06T13:51:20Z
dc.date.issued26/05/2017
dc.identifier.citationAhmedah HT, Patterson LH, Shnyder SD et al (2017) RGD-Binding Integrins in Head and Neck Cancers. Cancers. 9(6). 56.
dc.identifier.urihttp://hdl.handle.net/10454/12124
dc.descriptionYes
dc.description.abstractAlterations in integrin expression and function promote tumour growth, invasion, metastasis and neoangiogenesis. Head and neck cancers are highly vascular tumours with a tendency to metastasise. They express a wide range of integrin receptors. Expression of the αv and β1 subunits has been explored relatively extensively and linked to tumour progression and metastasis. Individual receptors αvβ3 and αvβ5 have proved popular targets for diagnostic and therapeutic agents but lesser studied receptors, such as αvβ6, αvβ8, and β1 subfamily members, also show promise. This review presents the current knowledge of integrin expression and function in squamous cell carcinoma of the head and neck (HNSCC), with a particular focus on the RGD-binding integrins, in order to highlight the potential of integrins as targets for personalised tumour specific identification and therapy.
dc.language.isoen
dc.rights© 2017 The Authors. This is an open access article distributed under the Creative Commons CC-BY license (https://creativecommons.org/licenses/by/4.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
dc.subjectβ1
dc.subjectβ3
dc.subjectβ6
dc.subjectArginine-glycine-aspartate
dc.subjectRGD
dc.subjectMetastasis
dc.subjectTreatment resistance
dc.subjectIntegrin αv
dc.titleRGD-Binding Integrins in Head and Neck Cancers
dc.status.refereedYes
dc.typeArticle
dc.type.versionPublished version
dc.identifier.doihttps://doi.org/10.3390/cancers9060056
dc.rights.licenseCC-BY
refterms.dateFOA2018-07-27T01:26:08Z
dc.openaccess.statusopenAccess
dc.date.accepted23/05/2017


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