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dc.contributor.authorTanveer, Ten
dc.contributor.authorM, Pen
dc.contributor.authorDavid, Hen
dc.contributor.authorRahat, AAen
dc.contributor.authorJacqueline, Wen
dc.contributor.authorPaul, Wen
dc.contributor.authorShaowei, Zen
dc.date.accessioned2019-06-09T11:55:12Z
dc.date.issued2019-03-06en
dc.identifier.issn2072-6694en
dc.identifier.urihttp://hdl.handle.net/10026.1/14272
dc.description.abstract

Overexpression and secretion of the enzymes cathepsin D (CathD) and cathepsin L (CathL) is associated with metastasis in several human cancers. As a superfamily, extracellularly, these proteins may act within the tumor microenvironment to drive cancer progression, proliferation, invasion and metastasis. Therefore, it is important to discover novel therapeutic treatment strategies to target CathD and CathL and potentially impede metastasis. Graphene oxide (GO) could form the basis of such a strategy by acting as an adsorbent for pro-metastatic enzymes. Here, we have conducted research into the potential of targeted anti-metastatic therapy using GO to adsorb these pro-tumorigenic enzymes. Binding of CathD/L to GO revealed that CathD/L were adsorbed onto the surface of GO through its cationic and hydrophilic residues. This work could provide a roadmap for the rational integration of CathD/L-targeting agents into clinical settings.

en
dc.language.isoenen
dc.publisherMDPIen
dc.titleGraphene Oxide-Based Targeting of Extracellular Cathepsin D and Cathepsin L As A Novel Anti-Metastatic Enzyme Cancer Therapyen
dc.typeJournal Article
plymouth.issue3en
plymouth.volume11en
plymouth.journalCancersen
dc.identifier.doi10.3390/cancers11030319en
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Science and Engineering
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA11 Computer Science and Informatics
dcterms.dateAccepted2019-02-27en
dc.rights.embargodate2019-06-11en
dc.rights.embargoperiodNot knownen
rioxxterms.versionAMen
rioxxterms.versionofrecord10.3390/cancers11030319en
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserveden
rioxxterms.licenseref.startdate2019-03-06en
rioxxterms.typeJournal Article/Reviewen


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