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dc.contributor.authorTabish, TA
dc.contributor.authorPranjol, MZI
dc.contributor.authorWhatmore, JL
dc.contributor.authorZhang, S
dc.date.accessioned2020-05-06T12:59:36Z
dc.date.issued2020-05-06
dc.description.abstractAngiogenesis, tissue invasion and metastasis in the tumour microenvironment are all critical hallmarks of cancer. Upregulation of cathepsin L plays an important role in angiogenesis and metastasis through its ability to degrade the extracellular matrix, facilitating tissue remodeling and tumour cell invasion. Thus, cathepsin L is a potential therapeutic target for anticancer nanomedicine, with its inhibition emerging as an innovative and potentially promising therapeutic intervention for the development of anti-invasion and anti-metastatic enzyme therapies. Nanotechnology-based platforms have been extensively tested in the anti-cancer nanomedicine field with effective anti-tumour efficacy. These nanodrugs can suppress tumour cell proliferation, thereby reducing tumour growth. Recently, nanomedicinal approaches have also emerged as effective anti-metastatic strategies, including the use of graphene oxide and gold nanoparticles. With a focus on recent advances in developing nanotechnology to inhibit cathepsin L, this review provides an in-depth examination of this stimulating field in the context of tumour microenvironments. Innovative anti-metastatic agents may lead to new options for the treatment of cancers.en_GB
dc.description.sponsorshipEngineering and Physical Sciences Research Council (EPSRC)en_GB
dc.description.sponsorshipFORCE Cancer Charityen_GB
dc.identifier.citationVol. 2, article 1en_GB
dc.identifier.doi10.3389/fnano.2020.00001
dc.identifier.grantnumberEP/L015331/1en_GB
dc.identifier.grantnumber50703en_GB
dc.identifier.urihttp://hdl.handle.net/10871/120950
dc.language.isoenen_GB
dc.publisherFrontiers Mediaen_GB
dc.rights© 2020 Tabish, Pranjol, Whatmore and Zhang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.en_GB
dc.subjectnanomedicineen_GB
dc.subjectgrapheneen_GB
dc.subjectnanopartciclesen_GB
dc.subjectcathepsin Len_GB
dc.subjectcanceren_GB
dc.titleStatus and Future Directions of Anti-metastatic Cancer Nanomedicines for the Inhibition of Cathepsin Len_GB
dc.typeArticleen_GB
dc.date.available2020-05-06T12:59:36Z
dc.descriptionThis is the final version. Available on open access from Frontiers Media via the DOI in this recorden_GB
dc.identifier.journalFrontiers in Nanotechnologyen_GB
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2020-04-09
exeter.funder::FORCE Cancer Charityen_GB
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2020-04-09
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2020-05-06T12:57:55Z
refterms.versionFCDVoR
refterms.dateFOA2020-05-06T12:59:42Z
refterms.panelAen_GB


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© 2020 Tabish, Pranjol, Whatmore and Zhang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
Except where otherwise noted, this item's licence is described as © 2020 Tabish, Pranjol, Whatmore and Zhang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.