Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/19977
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dc.contributor.authorAnderson, Robin L-
dc.contributor.authorBalasas, Theo-
dc.contributor.authorCallaghan, Juliana-
dc.contributor.authorCoombes, R Charles-
dc.contributor.authorEvans, Jeff-
dc.contributor.authorHall, Jacqueline A-
dc.contributor.authorKinrade, Sally-
dc.contributor.authorJones, David-
dc.contributor.authorJones, Paul S-
dc.contributor.authorJones, Rob-
dc.contributor.authorMarshall, John F-
dc.contributor.authorPanico, Maria Beatrice-
dc.contributor.authorShaw, Jacqui A-
dc.contributor.authorSteeg, Patricia S-
dc.contributor.authorSullivan, Mark-
dc.contributor.authorTong, Warwick-
dc.contributor.authorWestwell, Andrew D-
dc.contributor.authorRitchie, James W A-
dc.date2018-12-04-
dc.date.accessioned2019-01-02T01:13:21Z-
dc.date.available2019-01-02T01:13:21Z-
dc.date.issued2019-
dc.identifier.citationNature reviews. Clinical oncology 2019; 16(3): 185-204-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/19977-
dc.description.abstractMost cancer-related deaths are a result of metastasis, and thus the importance of this process as a target of therapy cannot be understated. By asking 'how can we effectively treat cancer?', we do not capture the complexity of a disease encompassing >200 different cancer types - many consisting of multiple subtypes - with considerable intratumoural heterogeneity, which can result in variable responses to a specific therapy. Moreover, we have much less information on the pathophysiological characteristics of metastases than is available for the primary tumour. Most disseminated tumour cells that arrive in distant tissues, surrounded by unfamiliar cells and a foreign microenvironment, are likely to die; however, those that survive can generate metastatic tumours with a markedly different biology from that of the primary tumour. To treat metastasis effectively, we must inhibit fundamental metastatic processes and develop specific preclinical and clinical strategies that do not rely on primary tumour responses. To address this crucial issue, Cancer Research UK and Cancer Therapeutics CRC Australia formed a Metastasis Working Group with representatives from not-for-profit, academic, government, industry and regulatory bodies in order to develop recommendations on how to tackle the challenges associated with treating (micro)metastatic disease. Herein, we describe the challenges identified as well as the proposed approaches for discovering and developing anticancer agents designed specifically to prevent or delay the metastatic outgrowth of cancer.-
dc.language.isoeng-
dc.titleA framework for the development of effective anti-metastatic agents.-
dc.typeJournal Article-
dc.identifier.journaltitleNature reviews. Clinical oncology-
dc.identifier.affiliationWomen's Malignancies Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USAen
dc.identifier.affiliationResearch and Innovation Services, University of Portsmouth, Portsmouth, Hampshire, UKen
dc.identifier.affiliationCommercial Partnerships, Cancer Research UK (CRUK), London, UKen
dc.identifier.affiliationCancer Therapeutics Cooperative Research Centre (CTx), Melbourne, Victoria, Australiaen
dc.identifier.affiliationOlivia Newton-John Cancer Research Institute, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationSchool of Cancer Medicine, La Trobe University, Bundoora, Victoria, Australiaen
dc.identifier.affiliationMedicines Development for Global Health, Southbank, Victoria, Australiaen
dc.identifier.affiliationCentre for Drug Development, CRUK, London, UKen
dc.identifier.affiliationSchool of Pharmacy and Pharmaceutical Sciences, Cardiff University, Cardiff, Wales, UKen
dc.identifier.affiliationLeicester Cancer Research Centre, University of Leicester, Leicester, Leicestershire, UKen
dc.identifier.affiliationMedicines and Healthcare Products Regulatory Agency, London, UKen
dc.identifier.affiliationQueen Mary University of London, Barts Cancer Institute, London, UKen
dc.identifier.affiliationInstitute of Cancer Sciences, University of Glasgow, Glasgow, Scotland, UKen
dc.identifier.affiliationCentre for Drug Development, CRUK, London, UKen
dc.identifier.affiliationResearch and Development, Vivacitv Ltd, Chesham, Buckinghamshire, UKen
dc.identifier.affiliationDepartment of Surgery and Cancer, Imperial College London, Hammersmith Hospital, London, UKen
dc.identifier.doi10.1038/s41571-018-0134-8-
dc.identifier.orcid0000-0002-6841-7422-
dc.identifier.pubmedid30514977-
dc.type.austinJournal Article-
dc.type.austinReview-
local.name.researcherAnderson, Robin L
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
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