Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16757
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dc.contributor.authorCharmsaz, Sara-
dc.contributor.authorScott, Andrew M-
dc.contributor.authorBoyd, Andrew W-
dc.date2017-07-24-
dc.date.accessioned2017-08-02T05:24:02Z-
dc.date.available2017-08-02T05:24:02Z-
dc.date.issued2017-10-
dc.identifier.citationExperimental Hematology 2017; 54: 31-39en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/16757-
dc.description.abstractThe use of monoclonal antibodies and molecules derived from them has achieved considerable attention and success in recent years establishing this mode of therapy as important therapeutic strategy in many cancers and in particular in hematological tumors. Monoclonal antibodies recognize cell surface antigens expressed on target cells and mediate their function through various mechanisms, such as antibody-dependent cellular cytotoxicity, complement-dependent cytotoxicity or by modulating the immune system. The efficacy of monoclonal antibody therapy can be improved when conjugates to a highly potent payloads including cytotoxic drugs and radiolabelled isotopes. The Eph family of protein has received considerable attention in recent years as therapeutic targets for treatment of both solid and hematological cancers. High expression of Eph receptors on cancer cells in comparison to low expression levels in normal adult tissues makes them an attractive candidate for cancer immunotherapeutic. In this review we will detail the modes of action of antibody based therapies and will focus on the Eph family of proteins as potential targets for therapy in hematological malignancies.en_US
dc.subjectCanceren_US
dc.subjectEphen_US
dc.subjectHematological malignanciesen_US
dc.subjectMonoclonal antibodyen_US
dc.subjectTherapeutic targetingen_US
dc.titleTargeted therapies in hematological malignancies using therapeutic monoclonal antibodies against eph family receptorsen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleExperimental Hematologyen_US
dc.identifier.affiliationLeukaemia Foundation Laboratory, QIMR-Berghofer Medical Research Institute, Brisbane, Australiaen_US
dc.identifier.affiliationDepartment of Medicine, University of Queensland, Brisbane, Australiaen_US
dc.identifier.affiliationDepartment of Surgery, Royal College of Surgeons, Dublin, Irelanden_US
dc.identifier.affiliationOlivia Newton-John Cancer Research Institute, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationSchool of Cancer Medicine, La Trobe University, Melbourne, Australiaen_US
dc.identifier.affiliationDepartment of Medicine, University of Melbourne, Melbourne, Australiaen_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/28751189en_US
dc.identifier.doi10.1016/j.exphem.2017.07.003en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-6656-295Xen_US
dc.type.austinJournal Articleen_US
local.name.researcherScott, Andrew M
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
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