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dc.contributor.authorSveinbjørnsson, Baldur
dc.contributor.authorCamilio, Ketil Andre
dc.contributor.authorHaug, Bengt Erik
dc.contributor.authorRekdal, Øystein
dc.date.accessioned2018-07-10T11:26:33Z
dc.date.available2018-07-10T11:26:33Z
dc.date.issued2017-05-08
dc.description.abstractThe oncolytic peptide LTX-315, which has been <i>de novo</i> designed based on structure– activity relationship studies of host defense peptides, has the ability to kill human cancer cells and induce specific anticancer immune response when injected locally into tumors established in immunocompetent mice. The oncolytic effect of LTX-315 involves perturbation of plasma membrane and the mitochondria with subsequent release of danger-associated molecular pattern molecules, which highlights the ability of LTX315 to induce complete regression and protective immune responses. Treatment with LTX-315 reprograms the tumor microenvironment by decreasing the local abundance of immunosuppressive cells and by increasing the frequency of effector T cells.en_US
dc.descriptionSource at: <a href=http://doi.org/10.4155/fmc-2017-0088> http://doi.org/10.4155/fmc-2017-0088</a>en_US
dc.identifier.citationSveinbjørnsson, B., Camilio, K. A., Haug, B. E. & Rekdal, Ø. (2017). LTX-315: a first-in-class oncolytic peptide that reprograms the tumor microenvironment. Future Medicinal Chemistry, 9(12), 1339-1344. http://doi.org/10.4155/fmc-2017-0088en_US
dc.identifier.cristinIDFRIDAID 1485292
dc.identifier.doi10.4155/fmc-2017-0088
dc.identifier.issn1756-8919
dc.identifier.issn1756-8927
dc.identifier.urihttps://hdl.handle.net/10037/13209
dc.language.isoengen_US
dc.publisherFuture Scienceen_US
dc.relation.journalFuture Medicinal Chemistry
dc.rights.accessRightsopenAccessen_US
dc.subjectVDP::Matematikk og Naturvitenskap: 400::Kjemi: 440en_US
dc.subjectVDP::Mathematics and natural science: 400::Chemistry: 440en_US
dc.titleLTX-315: a first-in-class oncolytic peptide that reprograms the tumor microenvironmenten_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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