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dc.contributor.authorLi, J-L
dc.contributor.authorJubb, AM
dc.contributor.authorHarris, AL
dc.date.accessioned2017-11-27T16:47:06Z
dc.date.available2017-11-27T16:47:06Z
dc.date.issued2010-07
dc.identifier.issn1479-6694
dc.identifier.issn1744-8301
dc.identifier.urihttp://hdl.handle.net/10026.1/10312
dc.description.abstract

<jats:p>Evaluation of: Yan M, Callahan CA, Beyer JC et al.: Chronic DLL4 blockade induces vascular neoplasms. Nature 463, E6–E7 (2010). Delta-like ligand 4 (DLL4) is a Notch ligand that is critical in the formation of a functional vascular network in tumors. Blockade of DLL4-mediated Notch signaling strikingly increases nonproductive angiogenesis, but significantly inhibits tumor growth in preclinical mouse models. Thus, DLL4 has emerged as an attractive target for cancer therapy. Anti-DLL4 antibodies have recently entered clinical trials. However, the potential toxic effects of anti-DLL4 are poorly understood. In this article, Yan et al. reported that chronic DLL4 blockade abnormally activates endothelial cells, causes pathological changes of multiple organs and induces vascular neoplasms. The findings need confirmation in further studies using different tumor-bearing animals but, nevertheless, raise important safety concerns regarding the use of anti-DLL4 agents and warrant monitoring for these effects in clinical trials for targeting DLL4.</jats:p>

dc.format.extent1099-1103
dc.format.mediumPrint
dc.languageen
dc.language.isoeng
dc.publisherFuture Medicine Ltd
dc.subjectangiogenesis
dc.subjectanti-DLL4 therapy
dc.subjectDLL4
dc.subjectNotch signaling
dc.subjectvascular neoplasm
dc.subjectxenograft
dc.titleTargeting DLL4 in tumors shows preclinical activity but potentially significant toxicity
dc.typejournal-article
dc.typeEditorial Material
plymouth.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/20624122
plymouth.issue7
plymouth.volume6
plymouth.publication-statusPublished
plymouth.journalFuture Oncology
dc.identifier.doi10.2217/fon.10.62
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA01 Clinical Medicine
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA01 Clinical Medicine/UoA01 Clinical Medicine
dc.publisher.placeEngland
dc.identifier.eissn1744-8301
dc.rights.embargoperiodNot known
rioxxterms.versionofrecord10.2217/fon.10.62
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.typeJournal Article/Review


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