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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1016/j.ctarc.2021.100355</dc:identifier><dc:language>eng</dc:language><dc:creator>Al-Wasaby, S.</dc:creator><dc:creator>Guerrero-Ochoa, P.</dc:creator><dc:creator>Ibáñez-Pérez, R.</dc:creator><dc:creator>Soler, R.</dc:creator><dc:creator>Conde, B.</dc:creator><dc:creator>Martínez-Lostao, L.</dc:creator><dc:creator>Anel, A.</dc:creator><dc:title>In vivo potential of recombinant granulysin against human melanoma</dc:title><dc:identifier>ART-2021-124382</dc:identifier><dc:description>9-kDa granulysin is a protein expressed into the granules of human cytotoxic T lymphocytes (CTL) and natural killer (NK) cells. It has been shown to exert cytolysis on microbes and tumors. We showed previously that 9-kDa granulysin exerted cell death by apoptosis in vitro on hematological tumor cell lines and also on cells from B-cell chronic lymphocytic leukemia (B-CLL) patients. In addition, we have shown the anti-tumor efficiency of granulysin as a single agent in two in vivo models of human tumor development in athymic mice, the MDA-MB-231 mammary adenocarcinoma and the NCI-H929 multiple myeloma, without signs of overt secondary effects by itself. In this work, we have tested recombinant 9-kDa granulysin in an in vivo and especially aggressive model of melanoma development, xenografted UACC62 cells in athymic mice. Recombinant granulysin was administered once UACC62-derived tumors were detectable and it substantially retarded the in vivo development of this aggressive tumor. We could also detect apoptosis induction and increased NK cell infiltration inside granulysin-treated tumor tissues. These observations are especially interesting given the possibility of treating melanoma by intra-tumor injection.</dc:description><dc:date>2021</dc:date><dc:source>http://zaguan.unizar.es/record/102211</dc:source><dc:doi>10.1016/j.ctarc.2021.100355</dc:doi><dc:identifier>http://zaguan.unizar.es/record/102211</dc:identifier><dc:identifier>oai:zaguan.unizar.es:102211</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/B31-17R</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO/SAF2016-76338-R</dc:relation><dc:identifier.citation>Cancer Treatment and Research Communications 27 (2021), 100355 [7 pp.]</dc:identifier.citation><dc:rights>by-nc-nd</dc:rights><dc:rights>http://creativecommons.org/licenses/by-nc-nd/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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